| geneid | 6929 |
|---|---|
| ensemblid | ENSG00000071564.19 |
| hgncid | 11633 |
| symbol | TCF3 |
| name | transcription factor 3 |
| refseq_nuc | NM_003200.5 |
| refseq_prot | NP_003191.1 |
| ensembl_nuc | ENST00000262965.12 |
| ensembl_prot | ENSP00000262965.5 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 1609292 |
| end | 1652615 |
| strand | - |
| ver | v1.2 |
| region | chr19:1609292-1652615 |
| region5000 | chr19:1604292-1657615 |
| regionname0 | TCF3_chr19_1609292_1652615 |
| regionname5000 | TCF3_chr19_1604292_1657615 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 654 | 235 | 73 | 67 | 51 | 10 | 32 | 32 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002 | 0/0 | 654 | 57 | 0 | 9 | 46 | 0 | 2 | 35 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003 | 0/0 | 654 | 37 | 3 | 0 | 25 | 2 | 7 | 15 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0004 | 0/0 | 654 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0005 | 0/0 | 654 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0006 | 0/0 | 654 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0007 | 0/0 | 654 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0008 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0009 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0010 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0011 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0012 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0013 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0014 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0015 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0016 | 0/0 | 654 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0017 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0018 | 0/0 | 654 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0019 | 0/0 | 654 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0020 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0021 | 0/0 | 654 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1965 | 57 | 0 | 9 | 46 | 0 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0002 | 0/0 | 1965 | 57 | 32 | 9 | 12 | 0 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0003 | 1/1 | 1965 | 54 | 8 | 20 | 7 | 6 | 11 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0004 | 0/0 | 1965 | 47 | 11 | 25 | 6 | 3 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0005 | 0/0 | 1965 | 47 | 10 | 9 | 16 | 1 | 11 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0006 | 0/0 | 1965 | 29 | 1 | 0 | 24 | 1 | 3 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0007 | 0/0 | 1965 | 21 | 7 | 2 | 8 | 0 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0008 | 0/0 | 1965 | 5 | 0 | 0 | 0 | 1 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0009 | 0/0 | 1965 | 4 | 3 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0010 | 0/0 | 1965 | 3 | 3 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0011 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0012 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0013 | 0/0 | 1965 | 2 | 1 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0014 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0015 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0016 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0017 | 0/0 | 1965 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0018 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0019 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0020 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0021 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0022 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0023 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0024 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0025 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0026 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0027 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0028 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0029 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0030 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0031 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0032 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0033 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| c0034 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2771 | 63 | 20 | 12 | 14 | 5 | 10 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0002 | 0/0 | 2772 | 56 | 17 | 13 | 20 | 1 | 5 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0003 | 0/0 | 2771 | 17 | 6 | 9 | 0 | 2 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0004 | 0/0 | 2772 | 14 | 1 | 5 | 3 | 1 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0005 | 0/0 | 2773 | 13 | 3 | 3 | 4 | 0 | 3 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0006 | 0/0 | 2771 | 11 | 0 | 0 | 11 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0007 | 0/0 | 2770 | 11 | 0 | 0 | 10 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0008 | 0/0 | 2770 | 10 | 1 | 6 | 1 | 1 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0009 | 0/0 | 2771 | 8 | 0 | 4 | 3 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0010 | 0/0 | 2773 | 6 | 0 | 1 | 5 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0011 | 0/0 | 2772 | 6 | 0 | 4 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0012 | 0/0 | 2772 | 6 | 0 | 0 | 5 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0013 | 0/0 | 2770 | 5 | 5 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0014 | 0/0 | 2771 | 4 | 0 | 0 | 4 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0015 | 0/0 | 2771 | 4 | 0 | 3 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0016 | 0/0 | 2769 | 4 | 0 | 3 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0017 | 0/0 | 2773 | 4 | 0 | 0 | 3 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0018 | 0/0 | 2771 | 3 | 3 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0019 | 0/0 | 2772 | 3 | 0 | 0 | 3 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0020 | 0/0 | 2771 | 3 | 3 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0021 | 0/0 | 2772 | 3 | 2 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0022 | 0/0 | 2772 | 3 | 0 | 0 | 3 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0023 | 0/0 | 2773 | 2 | 0 | 0 | 1 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0024 | 0/0 | 2772 | 2 | 0 | 2 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0025 | 0/0 | 2774 | 2 | 0 | 0 | 0 | 0 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0026 | 0/0 | 2772 | 2 | 1 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0027 | 0/0 | 2771 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0028 | 0/0 | 2773 | 2 | 0 | 0 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0029 | 0/0 | 2771 | 2 | 0 | 2 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0030 | 0/0 | 2771 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0031 | 0/0 | 2770 | 2 | 1 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0032 | 0/0 | 2773 | 2 | 1 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0033 | 0/0 | 2774 | 2 | 0 | 0 | 1 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0034 | 0/0 | 2771 | 2 | 0 | 0 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0035 | 0/0 | 2774 | 2 | 1 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0036 | 0/0 | 2773 | 2 | 1 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0037 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0038 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0039 | 0/0 | 2771 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0040 | 0/0 | 2773 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0041 | 0/0 | 2773 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0042 | 0/0 | 2773 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0043 | 0/0 | 2773 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0044 | 0/0 | 2774 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0045 | 0/0 | 2773 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0046 | 0/0 | 2772 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0047 | 0/0 | 2774 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0048 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0049 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0050 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0051 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0052 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0053 | 0/0 | 2771 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0054 | 0/0 | 2785 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0055 | 0/0 | 2773 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0056 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0057 | 0/0 | 2772 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0058 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0059 | 0/0 | 2772 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0060 | 0/0 | 2771 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0061 | 0/0 | 2771 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0062 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0063 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0064 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0065 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0066 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0067 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0068 | 0/0 | 2771 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0069 | 0/0 | 2771 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0070 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0071 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0072 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0073 | 0/0 | 2770 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0074 | 0/0 | 2770 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0075 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0076 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0077 | 0/0 | 2771 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0078 | 0/0 | 2771 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0079 | 0/0 | 2770 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0080 | 0/0 | 2774 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0081 | 0/0 | 2773 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0082 | 0/0 | 2773 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0083 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0084 | 0/0 | 2771 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0085 | 0/0 | 2772 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0086 | 0/0 | 2771 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0087 | 0/0 | 2771 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0088 | 0/0 | 2771 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0089 | 0/0 | 2771 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0090 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0091 | 0/0 | 2773 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0092 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0093 | 0/0 | 2772 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0094 | 0/0 | 2773 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0095 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0096 | 0/0 | 2772 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0097 | 0/0 | 2774 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0098 | 0/0 | 2774 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0099 | 0/0 | 2774 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0100 | 0/0 | 2774 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0101 | 0/0 | 2774 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0102 | 0/0 | 2773 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| t0103 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1965 | 57 | 32 | 9 | 12 | 0 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003 | 1/1 | 1965 | 54 | 8 | 20 | 7 | 6 | 11 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004 | 0/0 | 1965 | 47 | 11 | 25 | 6 | 3 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005 | 0/0 | 1965 | 47 | 10 | 9 | 16 | 1 | 11 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007 | 0/0 | 1965 | 21 | 7 | 2 | 8 | 0 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0009 | 0/0 | 1965 | 4 | 3 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0013 | 0/0 | 1965 | 2 | 1 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0019 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0025 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0029 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001 | 0/0 | 1965 | 57 | 0 | 9 | 46 | 0 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006 | 0/0 | 1965 | 29 | 1 | 0 | 24 | 1 | 3 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0008 | 0/0 | 1965 | 5 | 0 | 0 | 0 | 1 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0011 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0028 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0004c0014 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0004c0033 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0005c0010 | 0/0 | 1965 | 3 | 3 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0006c0012 | 0/0 | 1965 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0007c0016 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0008c0032 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0009c0021 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0010c0023 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0011c0031 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0012c0030 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0013c0022 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0014c0020 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0015c0024 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0016c0027 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0017c0026 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0018c0018 | 0/0 | 1965 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0019c0017 | 0/0 | 1965 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0020c0034 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0021c0015 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 4735 | 19 | 10 | 4 | 4 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0002 | 0/0 | 4736 | 18 | 10 | 1 | 5 | 0 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0004 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0005 | 0/0 | 4737 | 4 | 2 | 0 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0013 | 0/0 | 4734 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0027 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0032 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0035 | 0/0 | 4738 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0036 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0041 | 0/0 | 4737 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0046 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0058 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0065 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0075 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0078 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0083 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0085 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0002t0093 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0001 | 1/1 | 4735 | 17 | 3 | 6 | 0 | 4 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0002 | 0/0 | 4736 | 16 | 4 | 7 | 2 | 0 | 3 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0005 | 0/0 | 4737 | 8 | 0 | 3 | 2 | 0 | 3 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0008 | 0/0 | 4734 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0009 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0010 | 0/0 | 4737 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0012 | 0/0 | 4736 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0028 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0032 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0033 | 0/0 | 4738 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0055 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0059 | 0/0 | 4736 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0060 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0076 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0077 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0003t0089 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0001 | 0/0 | 4735 | 2 | 1 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0002 | 0/0 | 4736 | 3 | 0 | 2 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0003 | 0/0 | 4735 | 16 | 5 | 9 | 0 | 2 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0008 | 0/0 | 4734 | 9 | 1 | 6 | 1 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0011 | 0/0 | 4736 | 6 | 0 | 4 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0021 | 0/0 | 4736 | 3 | 2 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0028 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0062 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0066 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0081 | 0/0 | 4737 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0086 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0094 | 0/0 | 4737 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0099 | 0/0 | 4738 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0004t0102 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0001 | 0/0 | 4735 | 5 | 3 | 0 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0002 | 0/0 | 4736 | 2 | 1 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0004 | 0/0 | 4736 | 12 | 1 | 3 | 3 | 1 | 4 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0009 | 0/0 | 4735 | 7 | 0 | 3 | 3 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0010 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0013 | 0/0 | 4734 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0017 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0023 | 0/0 | 4737 | 2 | 0 | 0 | 1 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0024 | 0/0 | 4736 | 2 | 0 | 2 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0025 | 0/0 | 4738 | 2 | 0 | 0 | 0 | 0 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0026 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0027 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0030 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0038 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0039 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0040 | 0/0 | 4737 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0044 | 0/0 | 4738 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0045 | 0/0 | 4737 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0047 | 0/0 | 4738 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0052 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0005t0097 | 0/0 | 4738 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0001 | 0/0 | 4735 | 3 | 0 | 0 | 1 | 0 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0002 | 0/0 | 4736 | 6 | 1 | 2 | 3 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0003 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0005 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0012 | 0/0 | 4736 | 2 | 0 | 0 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0020 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0031 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0071 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0074 | 0/0 | 4734 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0090 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0091 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0096 | 0/0 | 4736 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0007t0103 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0009t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0009t0049 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0009t0050 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0009t0098 | 0/0 | 4738 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0013t0037 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0013t0042 | 0/0 | 4737 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0019t0026 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0025t0010 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0001c0029t0002 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0001 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0006 | 0/0 | 4735 | 11 | 0 | 0 | 11 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0007 | 0/0 | 4734 | 10 | 0 | 0 | 9 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0014 | 0/0 | 4735 | 4 | 0 | 0 | 4 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0015 | 0/0 | 4735 | 4 | 0 | 3 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0016 | 0/0 | 4733 | 4 | 0 | 3 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0019 | 0/0 | 4736 | 3 | 0 | 0 | 3 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0022 | 0/0 | 4736 | 3 | 0 | 0 | 3 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0029 | 0/0 | 4735 | 2 | 0 | 2 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0034 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0053 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0054 | 0/0 | 4749 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0056 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0057 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0064 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0069 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0070 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0073 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0084 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0087 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0088 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0092 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0095 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0002c0001t0100 | 0/0 | 4738 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0001 | 0/0 | 4735 | 9 | 0 | 0 | 6 | 1 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0002 | 0/0 | 4736 | 7 | 0 | 0 | 7 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0010 | 0/0 | 4737 | 2 | 0 | 0 | 2 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0012 | 0/0 | 4736 | 3 | 0 | 0 | 3 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0017 | 0/0 | 4737 | 3 | 0 | 0 | 2 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0031 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0033 | 0/0 | 4738 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0035 | 0/0 | 4738 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0067 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0006t0080 | 0/0 | 4738 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0008t0001 | 0/0 | 4735 | 2 | 0 | 0 | 0 | 0 | 2 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0008t0068 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0008t0082 | 0/0 | 4737 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0008t0101 | 0/0 | 4738 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0011t0030 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0011t0063 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0003c0028t0043 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0004c0014t0013 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0004c0014t0079 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0004c0033t0036 | 0/0 | 4737 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0005c0010t0018 | 0/0 | 4735 | 3 | 3 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0006c0012t0020 | 0/0 | 4735 | 2 | 2 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0007c0016t0002 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0008c0032t0061 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0009c0021t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0010c0023t0051 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0011c0031t0048 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0012c0030t0002 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0013c0022t0007 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0014c0020t0034 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0015c0024t0072 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0016c0027t0004 | 0/0 | 4736 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0017c0026t0002 | 0/0 | 4736 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0018c0018t0001 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0019c0017t0001 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0020c0034t0010 | 0/0 | 4737 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| a0021c0015t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | copy fasta | chr19 | 1604292 | 1657615 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0027g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0032g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0035g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0036g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0041g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0046g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0058g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0065g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0075g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0078g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0083g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0085g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0002t0093g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0240 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0005g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0008g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0010g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0012g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0028g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0032g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0033g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0055g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0059g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0060g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0076g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0077g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0003t0089g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0011g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0011g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0011g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0011g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0011g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0011g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0021g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0021g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0021g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0028g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0062g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0066g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0081g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0086g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0094g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0099g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0004t0102g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0009g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0009g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0009g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0009g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0009g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0010g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0013g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0013g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0017g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0023g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0023g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0024g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0024g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0025g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0025g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0026g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0027g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0030g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0038g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0039g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0040g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0044g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0045g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0047g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0052g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0005t0097g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0012g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0012g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0020g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0031g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0071g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0074g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0090g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0091g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0096g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0007t0103g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0009t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0009t0049g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0009t0050g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0009t0098g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0013t0037g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0013t0042g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0019t0026g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0025t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0001c0029t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0014g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0014g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0014g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0015g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0015g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0015g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0015g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0016g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0016g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0016g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0019g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0019g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0019g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0022g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0022g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0022g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0029g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0029g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0034g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0053g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0054g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0056g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0057g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0064g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0069g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0070g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0073g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0084g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0087g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0088g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0092g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0095g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0002c0001t0100g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0010g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0010g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0012g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0012g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0012g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0017g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0017g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0017g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0031g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0033g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0035g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0067g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0006t0080g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0008t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0008t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0008t0068g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0008t0082g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0008t0101g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0011t0030g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0011t0063g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0003c0028t0043g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0004c0014t0013g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0004c0014t0079g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0004c0033t0036g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0005c0010t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0005c0010t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0005c0010t0018g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0006c0012t0020g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0006c0012t0020g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0007c0016t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0008c0032t0061g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0009c0021t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0010c0023t0051g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0011c0031t0048g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0012c0030t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0013c0022t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0014c0020t0034g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0015c0024t0072g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0016c0027t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0017c0026t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0018c0018t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0019c0017t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0020c0034t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| a0021c0015t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0165 | EUR | GBR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00099 | hp2 | a0001 | c0004 | t0003 | g0249 | EUR | GBR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00140 | hp1 | a0001 | c0003 | t0012 | g0333 | EUR | GBR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00140 | hp2 | a0001 | c0004 | t0003 | g0091 | EUR | GBR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0227 | EUR | FIN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00280 | hp2 | a0001 | c0003 | t0008 | g0098 | EUR | FIN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00323 | hp1 | a0003 | c0008 | t0068 | g0268 | EUR | FIN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0234 | EUR | FIN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00408 | hp1 | a0002 | c0001 | t0006 | g0076 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00408 | hp2 | a0001 | c0004 | t0102 | g0344 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00423 | hp1 | a0001 | c0007 | t0002 | g0259 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00423 | hp2 | a0017 | c0026 | t0002 | g0112 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00438 | hp1 | a0001 | c0003 | t0032 | g0237 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00438 | hp2 | a0003 | c0006 | t0002 | g0126 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00544 | hp1 | a0003 | c0006 | t0012 | g0313 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00544 | hp2 | a0014 | c0020 | t0034 | g0316 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00558 | hp1 | a0002 | c0001 | t0006 | g0074 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00558 | hp2 | a0003 | c0006 | t0002 | g0077 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00597 | hp1 | a0001 | c0004 | t0099 | g0343 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00597 | hp2 | a0003 | c0006 | t0035 | g0345 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00609 | hp1 | a0001 | c0005 | t0002 | g0224 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00609 | hp2 | a0002 | c0001 | t0088 | g0292 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00621 | hp1 | a0002 | c0001 | t0022 | g0318 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00621 | hp2 | a0003 | c0006 | t0012 | g0329 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00639 | hp1 | a0001 | c0004 | t0008 | g0097 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0228 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00642 | hp1 | a0001 | c0004 | t0003 | g0099 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00642 | hp2 | a0002 | c0001 | t0016 | g0269 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00673 | hp1 | a0002 | c0001 | t0007 | g0085 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00673 | hp2 | a0001 | c0005 | t0017 | g0293 | EAS | CHS | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00735 | hp1 | a0001 | c0004 | t0008 | g0256 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00735 | hp2 | a0001 | c0004 | t0011 | g0145 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00738 | hp1 | a0002 | c0001 | t0029 | g0159 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0275 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0095 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG00741 | hp2 | a0001 | c0004 | t0011 | g0135 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01069 | hp1 | a0001 | c0005 | t0024 | g0002 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01069 | hp2 | a0002 | c0001 | t0057 | g0158 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01070 | hp2 | a0002 | c0001 | t0016 | g0052 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01071 | hp1 | a0001 | c0005 | t0024 | g0003 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01074 | hp1 | a0001 | c0004 | t0011 | g0137 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01074 | hp2 | a0001 | c0003 | t0077 | g0241 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0214 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01081 | hp2 | a0001 | c0003 | t0060 | g0273 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01099 | hp1 | a0001 | c0003 | t0002 | g0274 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01099 | hp2 | a0001 | c0004 | t0008 | g0100 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01106 | hp1 | a0001 | c0004 | t0003 | g0109 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01106 | hp2 | a0001 | c0002 | t0085 | g0304 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01109 | hp1 | a0001 | c0002 | t0046 | g0039 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01109 | hp2 | a0004 | c0033 | t0036 | g0350 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01167 | hp1 | a0001 | c0005 | t0004 | g0028 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0226 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01168 | hp1 | a0001 | c0004 | t0008 | g0248 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01168 | hp2 | a0018 | c0018 | t0001 | g0164 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0230 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01169 | hp2 | a0001 | c0004 | t0008 | g0252 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01175 | hp1 | a0001 | c0013 | t0042 | g0033 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01175 | hp2 | a0001 | c0003 | t0005 | g0340 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01192 | hp1 | a0001 | c0002 | t0093 | g0341 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01192 | hp2 | a0001 | c0009 | t0098 | g0347 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01243 | hp1 | a0001 | c0004 | t0003 | g0246 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01243 | hp2 | a0001 | c0004 | t0003 | g0220 | AMR | PUR | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01255 | hp1 | a0001 | c0003 | t0010 | g0244 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01255 | hp2 | a0001 | c0004 | t0003 | g0105 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0216 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01256 | hp2 | a0001 | c0003 | t0009 | g0007 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0152 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01257 | hp2 | a0001 | c0004 | t0003 | g0153 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01261 | hp1 | a0001 | c0004 | t0021 | g0334 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0277 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01346 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0287 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01358 | hp1 | a0001 | c0004 | t0008 | g0250 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01358 | hp2 | a0002 | c0001 | t0015 | g0080 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01361 | hp1 | a0001 | c0005 | t0004 | g0023 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0166 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01433 | hp1 | a0001 | c0004 | t0094 | g0327 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01884 | hp1 | a0001 | c0002 | t0036 | g0348 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01884 | hp2 | a0005 | c0010 | t0018 | g0170 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01891 | hp2 | a0001 | c0007 | t0020 | g0289 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01934 | hp1 | a0001 | c0003 | t0005 | g0337 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01934 | hp2 | a0001 | c0005 | t0026 | g0037 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01943 | hp1 | a0001 | c0007 | t0002 | g0049 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0247 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0261 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01952 | hp2 | a0002 | c0001 | t0016 | g0050 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01975 | hp1 | a0001 | c0004 | t0002 | g0257 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01975 | hp2 | a0001 | c0004 | t0011 | g0136 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01978 | hp1 | a0002 | c0001 | t0015 | g0155 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01978 | hp2 | a0001 | c0004 | t0003 | g0047 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01981 | hp2 | a0001 | c0005 | t0009 | g0013 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01993 | hp1 | a0007 | c0016 | t0002 | g0260 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01993 | hp2 | a0001 | c0004 | t0086 | g0303 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02004 | hp1 | a0002 | c0001 | t0015 | g0081 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02004 | hp2 | a0001 | c0005 | t0009 | g0022 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02015 | hp1 | a0001 | c0004 | t0011 | g0134 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02027 | hp1 | a0001 | c0002 | t0005 | g0328 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02027 | hp2 | a0003 | c0006 | t0002 | g0114 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02055 | hp1 | a0001 | c0004 | t0003 | g0286 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02055 | hp2 | a0001 | c0002 | t0035 | g0349 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02056 | hp1 | a0002 | c0001 | t0019 | g0284 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02056 | hp2 | a0003 | c0006 | t0012 | g0314 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02071 | hp1 | a0001 | c0007 | t0002 | g0127 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02071 | hp2 | a0001 | c0003 | t0005 | g0325 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02083 | hp1 | a0002 | c0001 | t0007 | g0062 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02083 | hp2 | a0001 | c0029 | t0002 | g0162 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02129 | hp1 | a0001 | c0003 | t0055 | g0235 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0258 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02132 | hp1 | a0002 | c0001 | t0022 | g0308 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02132 | hp2 | a0001 | c0007 | t0001 | g0217 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02135 | hp1 | a0001 | c0002 | t0083 | g0307 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02135 | hp2 | a0003 | c0006 | t0002 | g0150 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0319 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0330 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02148 | hp1 | a0001 | c0004 | t0003 | g0279 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02148 | hp2 | a0001 | c0005 | t0004 | g0017 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02165 | hp1 | a0001 | c0005 | t0004 | g0008 | EAS | CDX | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | CDX | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02257 | hp1 | a0001 | c0002 | t0065 | g0176 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02257 | hp2 | a0001 | c0002 | t0032 | g0161 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02258 | hp1 | a0001 | c0004 | t0021 | g0312 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02258 | hp2 | a0001 | c0007 | t0103 | g0351 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02273 | hp1 | a0002 | c0001 | t0029 | g0156 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0255 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02293 | hp1 | a0001 | c0003 | t0005 | g0336 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02293 | hp2 | a0016 | c0027 | t0004 | g0020 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02300 | hp1 | a0001 | c0007 | t0002 | g0149 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02300 | hp2 | a0001 | c0004 | t0002 | g0154 | AMR | PEL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02451 | hp1 | a0004 | c0014 | t0079 | g0305 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02523 | hp1 | a0001 | c0007 | t0090 | g0306 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02523 | hp2 | a0002 | c0001 | t0095 | g0317 | EAS | KHV | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02602 | hp1 | a0001 | c0003 | t0005 | g0331 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0094 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02615 | hp1 | a0001 | c0009 | t0001 | g0177 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02615 | hp2 | a0003 | c0011 | t0030 | g0139 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02622 | hp1 | a0012 | c0030 | t0002 | g0163 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02622 | hp2 | a0010 | c0023 | t0051 | g0140 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02647 | hp2 | a0001 | c0004 | t0003 | g0285 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0096 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02683 | hp2 | a0003 | c0006 | t0001 | g0128 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0281 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02698 | hp2 | a0001 | c0007 | t0001 | g0232 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0183 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02717 | hp2 | a0001 | c0007 | t0003 | g0107 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02723 | hp1 | a0003 | c0006 | t0067 | g0130 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02723 | hp2 | a0001 | c0002 | t0013 | g0182 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02735 | hp1 | a0003 | c0008 | t0001 | g0118 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02735 | hp2 | a0001 | c0007 | t0001 | g0238 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02738 | hp1 | a0003 | c0008 | t0101 | g0346 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02738 | hp2 | a0001 | c0004 | t0081 | g0302 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0267 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02886 | hp1 | a0001 | c0002 | t0078 | g0189 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02886 | hp2 | a0001 | c0002 | t0013 | g0197 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02895 | hp1 | a0001 | c0005 | t0013 | g0194 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02895 | hp2 | a0006 | c0012 | t0020 | g0262 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02896 | hp1 | a0004 | c0014 | t0013 | g0288 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0200 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0201 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02897 | hp2 | a0001 | c0005 | t0013 | g0195 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02922 | hp1 | a0001 | c0004 | t0003 | g0104 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02922 | hp2 | a0001 | c0005 | t0001 | g0204 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02970 | hp1 | a0001 | c0003 | t0002 | g0242 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02970 | hp2 | a0001 | c0003 | t0076 | g0045 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03017 | hp1 | a0002 | c0001 | t0007 | g0069 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03017 | hp2 | a0001 | c0005 | t0004 | g0019 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0223 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03098 | hp1 | a0001 | c0004 | t0003 | g0280 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03098 | hp2 | a0001 | c0013 | t0037 | g0009 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03130 | hp1 | a0001 | c0005 | t0027 | g0193 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03130 | hp2 | a0015 | c0024 | t0072 | g0179 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03139 | hp1 | a0001 | c0004 | t0003 | g0044 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03209 | hp1 | a0001 | c0007 | t0005 | g0339 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0253 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03453 | hp1 | a0009 | c0021 | t0001 | g0254 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03486 | hp1 | a0001 | c0007 | t0071 | g0199 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0190 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03490 | hp1 | a0001 | c0007 | t0074 | g0090 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03490 | hp2 | a0019 | c0017 | t0001 | g0221 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0229 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03492 | hp2 | a0001 | c0007 | t0096 | g0311 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03516 | hp1 | a0001 | c0004 | t0021 | g0321 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | ESN | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0186 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0184 | AFR | GWD | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03579 | hp1 | a0001 | c0002 | t0075 | g0185 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03579 | hp2 | a0001 | c0009 | t0050 | g0168 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0270 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03654 | hp2 | a0001 | c0003 | t0005 | g0332 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03669 | hp1 | a0001 | c0005 | t0023 | g0032 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03669 | hp2 | a0001 | c0003 | t0033 | g0324 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0272 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0276 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03704 | hp1 | a0003 | c0008 | t0001 | g0113 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03704 | hp2 | a0001 | c0005 | t0040 | g0006 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03710 | hp1 | a0001 | c0003 | t0059 | g0187 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03710 | hp2 | a0003 | c0006 | t0017 | g0298 | SAS | PJL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03831 | hp1 | a0001 | c0004 | t0008 | g0103 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03831 | hp2 | a0001 | c0005 | t0047 | g0042 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03834 | hp1 | a0003 | c0006 | t0001 | g0148 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03834 | hp2 | a0001 | c0005 | t0009 | g0029 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03927 | hp1 | a0002 | c0001 | t0100 | g0342 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03927 | hp2 | a0001 | c0003 | t0089 | g0301 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03942 | hp1 | a0001 | c0003 | t0005 | g0326 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03942 | hp2 | a0001 | c0005 | t0004 | g0030 | SAS | BEB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04115 | hp1 | a0001 | c0005 | t0025 | g0034 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04115 | hp2 | a0001 | c0005 | t0004 | g0027 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04199 | hp1 | a0001 | c0005 | t0025 | g0038 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0271 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04204 | hp1 | a0001 | c0005 | t0004 | g0010 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04204 | hp2 | a0001 | c0005 | t0045 | g0040 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04228 | hp1 | a0003 | c0008 | t0082 | g0299 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG04228 | hp2 | a0001 | c0002 | t0041 | g0004 | SAS | STU | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0243 | AFR | YRI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | YRI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18612 | hp1 | a0002 | c0001 | t0014 | g0073 | EAS | CHB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18612 | hp2 | a0003 | c0006 | t0001 | g0125 | EAS | CHB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18747 | hp1 | a0002 | c0001 | t0007 | g0070 | EAS | CHB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18747 | hp2 | a0003 | c0006 | t0031 | g0129 | EAS | CHB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18906 | hp1 | a0001 | c0005 | t0052 | g0205 | AFR | YRI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18906 | hp2 | a0001 | c0007 | t0002 | g0282 | AFR | YRI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18944 | hp1 | a0001 | c0004 | t0028 | g0101 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18944 | hp2 | a0002 | c0001 | t0006 | g0055 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18945 | hp1 | a0002 | c0001 | t0006 | g0068 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18945 | hp2 | a0002 | c0001 | t0006 | g0067 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18947 | hp1 | a0002 | c0001 | t0092 | g0295 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18947 | hp2 | a0020 | c0034 | t0010 | g0146 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18948 | hp1 | a0002 | c0001 | t0019 | g0056 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18948 | hp2 | a0002 | c0001 | t0014 | g0059 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18950 | hp1 | a0003 | c0006 | t0080 | g0296 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18950 | hp2 | a0002 | c0001 | t0064 | g0053 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18952 | hp2 | a0001 | c0003 | t0002 | g0245 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18962 | hp1 | a0002 | c0001 | t0007 | g0061 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18962 | hp2 | a0001 | c0005 | t0009 | g0016 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18963 | hp1 | a0003 | c0006 | t0033 | g0315 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18963 | hp2 | a0002 | c0001 | t0006 | g0075 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18964 | hp1 | a0003 | c0006 | t0017 | g0294 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18966 | hp1 | a0003 | c0028 | t0043 | g0036 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18966 | hp2 | a0001 | c0003 | t0005 | g0338 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18969 | hp1 | a0002 | c0001 | t0054 | g0157 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18969 | hp2 | a0001 | c0004 | t0008 | g0151 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18970 | hp1 | a0003 | c0006 | t0001 | g0119 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18971 | hp1 | a0003 | c0006 | t0001 | g0160 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18971 | hp2 | a0002 | c0001 | t0070 | g0121 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18977 | hp1 | a0001 | c0005 | t0004 | g0026 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18977 | hp2 | a0001 | c0007 | t0002 | g0278 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18986 | hp1 | a0001 | c0005 | t0001 | g0207 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18986 | hp2 | a0002 | c0001 | t0006 | g0083 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18989 | hp1 | a0002 | c0001 | t0056 | g0206 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18989 | hp2 | a0003 | c0006 | t0017 | g0297 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18990 | hp1 | a0002 | c0001 | t0084 | g0290 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18990 | hp2 | a0001 | c0005 | t0039 | g0014 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18998 | hp1 | a0001 | c0005 | t0023 | g0015 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18998 | hp2 | a0002 | c0001 | t0053 | g0057 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19000 | hp1 | a0002 | c0001 | t0019 | g0084 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19000 | hp2 | a0001 | c0005 | t0004 | g0031 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19004 | hp1 | a0002 | c0001 | t0073 | g0079 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19004 | hp2 | a0001 | c0005 | t0009 | g0024 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19005 | hp1 | a0001 | c0007 | t0091 | g0300 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19005 | hp2 | a0001 | c0007 | t0012 | g0323 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19007 | hp1 | a0002 | c0001 | t0014 | g0058 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19007 | hp2 | a0003 | c0006 | t0002 | g0123 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19010 | hp1 | a0002 | c0001 | t0007 | g0065 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19010 | hp2 | a0003 | c0006 | t0010 | g0141 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19012 | hp2 | a0002 | c0001 | t0087 | g0291 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19030 | hp1 | a0001 | c0005 | t0002 | g0131 | AFR | LWK | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19030 | hp2 | a0001 | c0002 | t0058 | g0283 | AFR | LWK | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19043 | hp1 | a0001 | c0004 | t0062 | g0046 | AFR | LWK | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19043 | hp2 | a0001 | c0009 | t0049 | g0167 | AFR | LWK | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19055 | hp1 | a0002 | c0001 | t0007 | g0060 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19055 | hp2 | a0008 | c0032 | t0061 | g0211 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19056 | hp1 | a0003 | c0006 | t0001 | g0116 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19056 | hp2 | a0002 | c0001 | t0007 | g0054 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19057 | hp1 | a0001 | c0005 | t0001 | g0208 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19057 | hp2 | a0002 | c0001 | t0006 | g0072 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19060 | hp1 | a0001 | c0005 | t0044 | g0041 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19060 | hp2 | a0002 | c0001 | t0016 | g0051 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19063 | hp1 | a0013 | c0022 | t0007 | g0066 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19063 | hp2 | a0001 | c0025 | t0010 | g0266 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19064 | hp1 | a0001 | c0002 | t0005 | g0322 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19064 | hp2 | a0002 | c0001 | t0022 | g0310 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19065 | hp1 | a0003 | c0006 | t0001 | g0115 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19065 | hp2 | a0002 | c0001 | t0007 | g0071 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19066 | hp1 | a0002 | c0001 | t0014 | g0087 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19066 | hp2 | a0002 | c0001 | t0006 | g0063 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19068 | hp1 | a0002 | c0001 | t0069 | g0082 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19068 | hp2 | a0001 | c0007 | t0012 | g0335 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19070 | hp2 | a0003 | c0006 | t0002 | g0120 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19074 | hp1 | a0003 | c0006 | t0010 | g0124 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19077 | hp1 | a0002 | c0001 | t0007 | g0064 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19077 | hp2 | a0003 | c0006 | t0001 | g0142 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19078 | hp1 | a0001 | c0003 | t0028 | g0144 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19078 | hp2 | a0011 | c0031 | t0048 | g0043 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19080 | hp2 | a0002 | c0001 | t0034 | g0309 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19081 | hp1 | a0002 | c0001 | t0015 | g0088 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19081 | hp2 | a0001 | c0005 | t0009 | g0021 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19084 | hp1 | a0001 | c0005 | t0010 | g0117 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19084 | hp2 | a0001 | c0005 | t0097 | g0320 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19085 | hp1 | a0003 | c0006 | t0002 | g0147 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19085 | hp2 | a0001 | c0005 | t0038 | g0025 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19091 | hp1 | a0001 | c0004 | t0011 | g0102 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19091 | hp2 | a0002 | c0001 | t0006 | g0086 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | YRI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA19240 | hp2 | a0001 | c0004 | t0066 | g0172 | AFR | YRI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20129 | hp1 | a0001 | c0004 | t0008 | g0251 | AFR | ASW | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20129 | hp2 | a0001 | c0005 | t0004 | g0011 | AFR | ASW | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20752 | hp1 | a0003 | c0006 | t0001 | g0092 | EUR | TSI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0233 | EUR | TSI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0108 | EUR | TSI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20805 | hp2 | a0001 | c0005 | t0004 | g0005 | EUR | TSI | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01123 | hp1 | a0001 | c0005 | t0009 | g0018 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG01123 | hp2 | a0001 | c0004 | t0003 | g0106 | AMR | CLM | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02486 | hp1 | a0003 | c0011 | t0063 | g0093 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02486 | hp2 | a0006 | c0012 | t0020 | g0263 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG02559 | hp2 | a0005 | c0010 | t0018 | g0171 | AFR | ACB | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03471 | hp1 | a0021 | c0015 | t0001 | g0231 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG03471 | hp2 | a0005 | c0010 | t0018 | g0169 | AFR | MSL | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0225 | AFR | USA | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| HG06807 | hp2 | a0001 | c0002 | t0027 | g0196 | AFR | USA | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18955 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA18955 | hp2 | a0002 | c0001 | t0006 | g0089 | EAS | JPT | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20300 | hp1 | a0001 | c0019 | t0026 | g0035 | AFR | USA | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | USA | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA21309 | hp1 | a0001 | c0005 | t0030 | g0192 | AFR | LWK | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| NA21309 | hp2 | a0001 | c0007 | t0031 | g0239 | AFR | LWK | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0236 | REF | REF | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0240 | REF | REF | TCF3_chr19_1604292_1657615 | TCF3 | chr19 | 1604292 | 1657615 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1611727
|
T | G | 1 | a0010 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1945A>C | p.Asn649His | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2300/4735 | 1945/1965 | 649/654 | chr19 | 1611727 | ||
| chr19:1611777
|
T | C | 1 | a0011 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.1895A>G | p.Asp632Gly | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2250/4735 | 1895/1965 | 632/654 | chr19 | 1611777 | ||
| chr19:1611790
|
C | G | 1 | a0012 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1882G>C | p.Gly628Arg | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2237/4735 | 1882/1965 | 628/654 | chr19 | 1611790 | ||
| chr19:1615692
|
C | T | 1 | a0009 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.1580G>A | p.Arg527Gln | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/19 | 1935/4735 | 1580/1965 | 527/654 | chr19 | 1615692 | ||
| chr19:1615717
|
T | C | 1 | a0008 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.1555A>G | p.Lys519Glu | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/19 | 1910/4735 | 1555/1965 | 519/654 | chr19 | 1615717 | ||
| chr19:1615733
|
G | C | 1 | a0005 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.1539C>G | p.His513Gln | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/19 | 1894/4735 | 1539/1965 | 513/654 | chr19 | 1615733 | ||
| chr19:1615776
|
C | A | 1 | a0006 | 2 | HG02486.hp2 HG02895.hp2 |
missense_variant | MODERATE | c.1496G>T | p.Arg499Leu | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/19 | 1851/4735 | 1496/1965 | 499/654 | chr19 | 1615776 | ||
| chr19:1615780
|
T | G | 1 | a0013 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1492A>C | p.Lys498Gln | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/19 | 1847/4735 | 1492/1965 | 498/654 | chr19 | 1615780 | ||
| chr19:1615797
|
G | A | 3 | a0002a0013a0014 | 59 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
missense_variant | MODERATE | c.1475C>T | p.Ala492Val | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/19 | 1830/4735 | 1475/1965 | 492/654 | chr19 | 1615797 | ||
| chr19:1619351
|
C | T | 5 | a0003a0006a0014others(2): Show | 42 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(39): Show |
missense_variant | MODERATE | c.1291G>A | p.Gly431Ser | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 15/19 | 1646/4735 | 1291/1965 | 431/654 | chr19 | 1619351 | ||
| chr19:1619371
|
G | A | 1 | a0015 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1271C>T | p.Ala424Val | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 15/19 | 1626/4735 | 1271/1965 | 424/654 | chr19 | 1619371 | ||
| chr19:1621901
|
C | T | 1 | a0016 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.892G>A | p.Gly298Arg | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/19 | 1247/4735 | 892/1965 | 298/654 | chr19 | 1621901 | ||
| chr19:1622069
|
G | C | 1 | a0017 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.807C>G | p.His269Gln | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 10/19 | 1162/4735 | 807/1965 | 269/654 | chr19 | 1622069 | ||
| chr19:1622373
|
T | C | 2 | a0004a0005 | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp1 others(3): Show |
missense_variant | MODERATE | c.592A>G | p.Thr198Ala | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 9/19 | 947/4735 | 592/1965 | 198/654 | chr19 | 1622373 | ||
| chr19:1625585
|
C | T | 1 | a0018 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.490G>A | p.Gly164Ser | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/19 | 845/4735 | 490/1965 | 164/654 | chr19 | 1625585 | ||
| chr19:1627366
|
A | G | 1 | a0019 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.359T>C | p.Leu120Pro | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/19 | 714/4735 | 359/1965 | 120/654 | chr19 | 1627366 | ||
| chr19:1627378
|
C | T | 1 | a0007 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.347G>A | p.Gly116Asp | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/19 | 702/4735 | 347/1965 | 116/654 | chr19 | 1627378 | ||
| chr19:1627400
|
C | A | 1 | a0020 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.325G>T | p.Ala109Ser | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/19 | 680/4735 | 325/1965 | 109/654 | chr19 | 1627400 | ||
| chr19:1646364
|
C | T | 1 | a0021 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.136G>A | p.Gly46Arg | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/19 | 491/4735 | 136/1965 | 46/654 | chr19 | 1646364 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1615376
|
T | C | 1 | a0001c0013 | 2 | HG01175.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1731A>G | p.Gln577Gln | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/19 | 2086/4735 | 1731/1965 | 577/654 | chr19 | 1615376 | ||
| chr19:1615796
|
C | T | 1 | a0001c0029 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1476G>A | p.Ala492Ala | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/19 | 1831/4735 | 1476/1965 | 492/654 | chr19 | 1615796 | ||
| chr19:1619148
|
G | A | 1 | a0010c0023 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1413C>T | p.Thr471Thr | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/19 | 1768/4735 | 1413/1965 | 471/654 | chr19 | 1619148 | ||
| chr19:1619334
|
G | A | 7 | a0001c0004a0001c0009a0003c0006others(4): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(81): Show |
synonymous_variant | LOW | c.1308C>T | p.Gly436Gly | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 15/19 | 1663/4735 | 1308/1965 | 436/654 | chr19 | 1619334 | ||
| chr19:1619340
|
T | C | 24 | a0001c0002a0001c0004a0001c0007others(21): Show | 242 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(239): Show |
synonymous_variant | LOW | c.1302A>G | p.Ser434Ser | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 15/19 | 1657/4735 | 1302/1965 | 434/654 | chr19 | 1619340 | ||
| chr19:1619349
|
G | A | 6 | a0003c0006a0003c0008a0003c0028others(3): Show | 38 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(35): Show |
synonymous_variant | LOW | c.1293C>T | p.Gly431Gly | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 15/19 | 1648/4735 | 1293/1965 | 431/654 | chr19 | 1619349 | ||
| chr19:1619454
|
G | A | 1 | a0015c0024 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1188C>T | p.His396His | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 15/19 | 1543/4735 | 1188/1965 | 396/654 | chr19 | 1619454 | ||
| chr19:1619795
|
C | G | 1 | a0001c0019 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1152G>C | p.Gly384Gly | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/19 | 1507/4735 | 1152/1965 | 384/654 | chr19 | 1619795 | ||
| chr19:1619801
|
G | A | 1 | a0001c0025 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.1146C>T | p.Tyr382Tyr | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/19 | 1501/4735 | 1146/1965 | 382/654 | chr19 | 1619801 | ||
| chr19:1620999
|
A | G | 3 | a0004c0014a0004c0033a0005c0010 | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp1 others(3): Show |
synonymous_variant | LOW | c.1062T>C | p.Ser354Ser | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/19 | 1417/4735 | 1062/1965 | 354/654 | chr19 | 1620999 | ||
| chr19:1622111
|
C | T | 1 | a0004c0014 | 2 | HG02451.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.765G>A | p.Pro255Pro | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 10/19 | 1120/4735 | 765/1965 | 255/654 | chr19 | 1622111 | ||
| chr19:1622117
|
G | A | 10 | a0001c0002a0001c0005a0001c0009others(7): Show | 116 | HG00609.hp1 HG00673.hp2 HG01069.hp1 others(113): Show |
synonymous_variant | LOW | c.759C>T | p.Ser253Ser | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 10/19 | 1114/4735 | 759/1965 | 253/654 | chr19 | 1622117 | ||
| chr19:1622407
|
T | C | 3 | a0004c0014a0004c0033a0005c0010 | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp1 others(3): Show |
synonymous_variant | LOW | c.558A>G | p.Pro186Pro | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 9/19 | 913/4735 | 558/1965 | 186/654 | chr19 | 1622407 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1609415
|
C | G | 1 | a0001c0007t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2292G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2292 | chr19 | 1609415 | |||||
| chr19:1609436
|
T | A | 54 | a0001c0002t0058a0001c0002t0083a0001c0003t0008others(51): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2271A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2271 | chr19 | 1609436 | |||||
| chr19:1609484
|
C | CT | 3 | a0001c0007t0103a0005c0010t0018a0010c0023t0051 | 5 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2222_*2223insA | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2222 | chr19 | 1609484 | |||||
| chr19:1609524
|
GC | G | 4 | a0002c0001t0016a0002c0001t0056a0002c0001t0064others(1): Show | 7 | HG00642.hp2 HG01070.hp2 HG01952.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2182delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2182 | chr19 | 1609524 | |||||
| chr19:1609525
|
C | T | 3 | a0001c0013t0037a0001c0013t0042a0003c0011t0063 | 3 | HG01175.hp1 HG02486.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2182G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2182 | chr19 | 1609525 | |||||
| chr19:1609549
|
C | G | 1 | a0001c0004t0062 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2158G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2158 | chr19 | 1609549 | |||||
| chr19:1609617
|
A | T | 27 | a0001c0007t0074a0001c0007t0090a0001c0007t0096others(24): Show | 60 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2090T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2090 | chr19 | 1609617 | |||||
| chr19:1609630
|
G | A | 1 | a0001c0002t0065 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2077C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2077 | chr19 | 1609630 | |||||
| chr19:1609668
|
C | T | 5 | a0002c0001t0014a0002c0001t0053a0002c0001t0070others(2): Show | 8 | HG02523.hp2 NA18612.hp1 NA18948.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2039G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2039 | chr19 | 1609668 | |||||
| chr19:1609670
|
T | C | 56 | a0001c0002t0058a0001c0002t0083a0001c0003t0008others(53): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*2037A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 2037 | chr19 | 1609670 | |||||
| chr19:1609759
|
G | A | 1 | a0003c0006t0067 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1948C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 1948 | chr19 | 1609759 | |||||
| chr19:1609761
|
C | T | 25 | a0001c0007t0074a0001c0007t0090a0001c0007t0096others(22): Show | 57 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 1946 | chr19 | 1609761 | |||||
| chr19:1609843
|
C | T | 1 | a0001c0003t0055 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1864G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 1864 | chr19 | 1609843 | |||||
| chr19:1609891
|
G | A | 4 | a0001c0003t0059a0003c0008t0068a0003c0008t0082others(1): Show | 4 | HG00323.hp1 HG02738.hp1 HG03710.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1816C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 1816 | chr19 | 1609891 | |||||
| chr19:1610363
|
C | T | 17 | a0001c0002t0083a0001c0003t0008a0001c0003t0028others(14): Show | 47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1344G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 1344 | chr19 | 1610363 | |||||
| chr19:1610557
|
G | A | 3 | a0002c0001t0015a0002c0001t0069a0002c0001t0073 | 6 | HG01358.hp2 HG01978.hp1 HG02004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1150C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 1150 | chr19 | 1610557 | |||||
| chr19:1610655
|
G | T | 1 | a0008c0032t0061 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 1052 | chr19 | 1610655 | |||||
| chr19:1610715
|
G | A | 2 | a0001c0007t0074a0001c0007t0096 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*992C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 992 | chr19 | 1610715 | |||||
| chr19:1610719
|
A | G | 3 | a0001c0007t0103a0005c0010t0018a0010c0023t0051 | 5 | HG01884.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*988T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 988 | chr19 | 1610719 | |||||
| chr19:1610785
|
C | T | 2 | a0001c0007t0020a0006c0012t0020 | 3 | HG01891.hp2 HG02486.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*922G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 922 | chr19 | 1610785 | |||||
| chr19:1610878
|
A | T | 2 | a0001c0003t0060a0001c0005t0024 | 3 | HG01069.hp1 HG01071.hp1 HG01081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*829T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 829 | chr19 | 1610878 | |||||
| chr19:1610924
|
C | CG | 48 | a0001c0002t0002a0001c0002t0004a0001c0002t0005others(45): Show | 125 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*782dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 782 | chr19 | 1610924 | |||||
| chr19:1610924
|
C | CGG | 18 | a0001c0003t0010a0001c0003t0028a0001c0003t0033others(15): Show | 21 | HG01192.hp2 HG01255.hp1 HG02129.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*781_*782dupCC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 782 | chr19 | 1610924 | |||||
| chr19:1610924
|
CG | C | 20 | a0001c0003t0008a0001c0003t0089a0001c0004t0008others(17): Show | 40 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*782delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 782 | chr19 | 1610924 | |||||
| chr19:1610938
|
G | A | 1 | a0010c0023t0051 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*769C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 769 | chr19 | 1610938 | |||||
| chr19:1610939
|
A | C | 1 | a0010c0023t0051 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 768 | chr19 | 1610939 | |||||
| chr19:1610940
|
C | G | 1 | a0010c0023t0051 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*767G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 767 | chr19 | 1610940 | |||||
| chr19:1610963
|
G | A | 1 | a0001c0005t0097 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*744C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 744 | chr19 | 1610963 | |||||
| chr19:1610998
|
T | C | 1 | a0001c0002t0075 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 709 | chr19 | 1610998 | |||||
| chr19:1611053
|
G | A | 1 | a0001c0002t0041 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*654C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 654 | chr19 | 1611053 | |||||
| chr19:1611178
|
A | AATGTTTT others(7): Show |
1 | a0002c0001t0054 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*515_*528dupGAAAAT others(8): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 528 | chr19 | 1611178 | |||||
| chr19:1611241
|
G | A | 1 | a0001c0007t0090 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 466 | chr19 | 1611241 | |||||
| chr19:1611320
|
T | C | 2 | a0001c0005t0038a0001c0005t0039 | 2 | NA18990.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*387A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 387 | chr19 | 1611320 | |||||
| chr19:1611373
|
G | GA | 7 | a0001c0002t0032a0001c0002t0041a0001c0003t0032others(4): Show | 7 | HG00438.hp1 HG02257.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*333dupT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 333 | chr19 | 1611373 | |||||
| chr19:1611373
|
GA | G | 14 | a0001c0002t0013a0001c0002t0027a0001c0002t0093others(11): Show | 18 | HG01192.hp1 HG01192.hp2 HG01884.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*333delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 333 | chr19 | 1611373 | |||||
| chr19:1611648
|
G | A | 1 | a0001c0003t0077 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*59C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 59 | chr19 | 1611648 | |||||
| chr19:1611697
|
G | A | 1 | a0001c0002t0078 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 19/19 | 10 | chr19 | 1611697 | |||||
| chr19:1650259
|
C | G | 3 | a0001c0009t0049a0001c0009t0050a0001c0009t0098 | 3 | HG01192.hp2 HG03579.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-11G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/19 | 11 | chr19 | 1650259 | |||||
| chr19:1652329
|
T | TG | 32 | a0001c0002t0035a0001c0002t0036a0001c0002t0083others(29): Show | 35 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-70dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/19 | 2082 | chr19 | 1652329 | |||||
| chr19:1652359
|
G | GC | 30 | a0001c0002t0005a0001c0002t0035a0001c0002t0036others(27): Show | 47 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-100dupG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/19 | 2112 | chr19 | 1652359 | |||||
| chr19:1652400
|
G | A | 1 | a0001c0007t0103 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-140C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/19 | 2152 | chr19 | 1652400 | |||||
| chr19:1652512
|
C | G | 1 | a0011c0031t0048 | 1 | NA19078.hp2 | 5_prime_UTR_variant | MODIFIER | c.-252G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/19 | 2264 | chr19 | 1652512 | |||||
| chr19:1652526
|
C | G | 21 | a0001c0002t0004a0001c0002t0041a0001c0002t0046others(18): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
5_prime_UTR_variant | MODIFIER | c.-266G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/19 | 2278 | chr19 | 1652526 | |||||
| chr19:1652545
|
C | G | 21 | a0001c0002t0004a0001c0002t0041a0001c0002t0046others(18): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
5_prime_UTR_variant | MODIFIER | c.-285G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/19 | 2297 | chr19 | 1652545 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:1611857
|
G | A | 45 | a0001c0003t0008g0098a0001c0003t0028g0144a0001c0003t0076g0045others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(42): Show |
splice_region_variant&intron_variant | LOW | c.1823-8C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611857 | ||||||
| chr19:1611918
|
G | T | 62 | a0001c0007t0074g0090a0001c0007t0090g0306a0001c0007t0096g0311others(59): Show | 62 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1823-69C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611918 | ||||||
| chr19:1611930
|
C | CG | 117 | a0001c0002t0001g0078a0001c0002t0001g0138a0001c0002t0001g0173others(114): Show | 117 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1823-82dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611930 | ||||||
| chr19:1611930
|
C | CGG | 26 | a0001c0002t0002g0191a0001c0002t0078g0189a0001c0003t0001g0200others(23): Show | 26 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1823-83_1823-82dup others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611930 | ||||||
| chr19:1611930
|
C | CGGG | 19 | a0001c0004t0003g0249a0001c0004t0003g0286a0001c0004t0008g0100others(16): Show | 19 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1823-84_1823-82dup others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611930 | ||||||
| chr19:1611932
|
G | C | 1 | a0001c0002t0005g0322 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1823-83C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611932 | ||||||
| chr19:1611933
|
G | A | 1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1823-84C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611933 | ||||||
| chr19:1611933
|
G | GA | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1823-85_1823-84ins others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611933 | ||||||
| chr19:1611935
|
G | T | 1 | a0001c0002t0005g0322 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1823-86C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611935 | ||||||
| chr19:1611940
|
G | C | 1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1823-91C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1611940 | ||||||
| chr19:1612123
|
G | A | 1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1823-274C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612123 | ||||||
| chr19:1612348
|
G | C | 1 | a0002c0001t0056g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1823-499C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612348 | ||||||
| chr19:1612350
|
A | G | 1 | a0002c0001t0056g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1823-501T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612350 | ||||||
| chr19:1612428
|
G | A | 1 | a0001c0007t0091g0300 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1823-579C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612428 | ||||||
| chr19:1612518
|
C | A | 2 | a0001c0002t0002g0190a0001c0002t0002g0191 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1823-669G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612518 | ||||||
| chr19:1612634
|
G | GGGTACAC others(28): Show |
3 | a0004c0014t0013g0288a0004c0014t0079g0305a0010c0023t0051g0140 | 3 | HG02451.hp1 HG02622.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1823-820_1823-786d others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612634 | ||||||
| chr19:1612685
|
T | G | 1 | a0002c0001t0034g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1823-836A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612685 | ||||||
| chr19:1612704
|
G | A | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1823-855C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612704 | ||||||
| chr19:1612720
|
T | C | 120 | a0001c0003t0008g0098a0001c0003t0028g0144a0001c0003t0076g0045others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1823-871A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612720 | ||||||
| chr19:1612720
|
T | TTGGTGTG others(63): Show |
3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1823-872_1823-871i others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612720 | ||||||
| chr19:1612739
|
G | A | 1 | a0001c0004t0008g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1823-890C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612739 | ||||||
| chr19:1612747
|
G | A | 44 | a0001c0003t0008g0098a0001c0003t0028g0144a0001c0003t0076g0045others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.1823-898C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612747 | ||||||
| chr19:1612818
|
G | A | 4 | a0001c0003t0076g0045a0001c0004t0003g0044a0001c0004t0003g0047others(1): Show | 4 | HG01978.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1823-969C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1612818 | ||||||
| chr19:1613038
|
T | C | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1823-1189A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613038 | ||||||
| chr19:1613057
|
G | C | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1823-1208C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613057 | ||||||
| chr19:1613130
|
G | C | 1 | a0003c0006t0001g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1823-1281C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613130 | ||||||
| chr19:1613140
|
C | T | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1823-1291G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613140 | ||||||
| chr19:1613152
|
CTGA | C | 62 | a0001c0007t0074g0090a0001c0007t0090g0306a0001c0007t0096g0311others(59): Show | 62 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.1823-1306_1823-130 others(7): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613152 | ||||||
| chr19:1613253
|
G | A | 2 | a0001c0007t0003g0107a0003c0011t0063g0093 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1823-1404C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613253 | ||||||
| chr19:1613258
|
C | T | 1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1823-1409G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613258 | ||||||
| chr19:1613259
|
G | T | 1 | a0001c0007t0103g0351 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1823-1410C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613259 | ||||||
| chr19:1613359
|
C | T | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1823-1510G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613359 | ||||||
| chr19:1613409
|
G | A | 3 | a0004c0014t0013g0288a0004c0014t0079g0305a0015c0024t0072g0179 | 3 | HG02451.hp1 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1823-1560C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613409 | ||||||
| chr19:1613593
|
G | A | 1 | a0001c0002t0013g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1822+1692C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613593 | ||||||
| chr19:1613595
|
A | C | 1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1822+1690T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613595 | ||||||
| chr19:1613609
|
C | A | 2 | a0001c0004t0003g0249a0001c0004t0008g0250 | 2 | HG00099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1822+1676G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613609 | ||||||
| chr19:1613679
|
G | A | 1 | a0002c0001t0001g0122 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1822+1606C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613679 | ||||||
| chr19:1613711
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1822+1574C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613711 | ||||||
| chr19:1613796
|
G | GT | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822+1488_1822+148 others(5): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613796 | ||||||
| chr19:1613848
|
A | G | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822+1437T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613848 | ||||||
| chr19:1613880
|
G | C | 1 | a0003c0006t0002g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1822+1405C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613880 | ||||||
| chr19:1613900
|
C | A | 1 | a0001c0002t0002g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1822+1385G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613900 | ||||||
| chr19:1613941
|
C | T | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1822+1344G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613941 | ||||||
| chr19:1613963
|
C | T | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822+1322G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613963 | ||||||
| chr19:1613982
|
C | T | 2 | a0005c0010t0018g0169a0005c0010t0018g0170 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1822+1303G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613982 | ||||||
| chr19:1613997
|
C | T | 3 | a0001c0004t0003g0105a0001c0004t0003g0106a0001c0004t0011g0145 | 3 | HG00735.hp2 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1822+1288G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1613997 | ||||||
| chr19:1614109
|
G | A | 1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1822+1176C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614109 | ||||||
| chr19:1614188
|
C | A | 8 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0002g0133others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1822+1097G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614188 | ||||||
| chr19:1614305
|
G | A | 1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1822+980C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614305 | ||||||
| chr19:1614326
|
G | T | 1 | a0002c0001t0095g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1822+959C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614326 | ||||||
| chr19:1614327
|
T | G | 1 | a0002c0001t0095g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1822+958A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614327 | ||||||
| chr19:1614359
|
G | T | 1 | a0001c0005t0025g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1822+926C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614359 | ||||||
| chr19:1614418
|
G | A | 1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1822+867C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614418 | ||||||
| chr19:1614454
|
G | A | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822+831C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614454 | ||||||
| chr19:1614479
|
G | A | 2 | a0001c0002t0001g0174a0001c0002t0085g0304 | 2 | HG01106.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1822+806C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614479 | ||||||
| chr19:1614712
|
T | A | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1822+573A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614712 | ||||||
| chr19:1614714
|
T | A | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1822+571A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614714 | ||||||
| chr19:1614779
|
G | A | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1822+506C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614779 | ||||||
| chr19:1614821
|
A | G | 125 | a0001c0002t0002g0175a0001c0002t0041g0004a0001c0003t0008g0098others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1822+464T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614821 | ||||||
| chr19:1614911
|
G | A | 36 | a0001c0002t0004g0012a0001c0005t0004g0005a0001c0005t0004g0010others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1822+374C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614911 | ||||||
| chr19:1614983
|
G | T | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822+302C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1614983 | ||||||
| chr19:1615046
|
A | G | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1822+239T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1615046 | ||||||
| chr19:1615153
|
A | C | 6 | a0001c0002t0001g0178a0001c0002t0001g0198a0001c0002t0002g0267others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822+132T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1615153 | ||||||
| chr19:1615203
|
G | A | 2 | a0001c0007t0074g0090a0001c0007t0096g0311 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1822+82C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 18/18 | chr19 | 1615203 | ||||||
| chr19:1615665
|
T | G | 7 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1586+21A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/18 | chr19 | 1615665 | ||||||
| chr19:1615669
|
G | A | 1 | a0001c0004t0008g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1586+17C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 17/18 | chr19 | 1615669 | ||||||
| chr19:1615847
|
C | T | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451-26G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1615847 | ||||||
| chr19:1615853
|
C | T | 48 | a0001c0003t0008g0098a0001c0003t0028g0144a0001c0003t0076g0045others(45): Show | 48 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.1451-32G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1615853 | ||||||
| chr19:1615947
|
CA | C | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1451-127delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1615947 | ||||||
| chr19:1615968
|
T | C | 4 | a0001c0003t0001g0261a0001c0003t0005g0336a0001c0007t0002g0049others(1): Show | 4 | HG01943.hp1 HG01952.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1451-147A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1615968 | ||||||
| chr19:1616041
|
G | A | 3 | a0001c0003t0002g0245a0001c0003t0032g0237a0001c0007t0091g0300 | 3 | HG00438.hp1 NA18952.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1451-220C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616041 | ||||||
| chr19:1616061
|
A | G | 1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1451-240T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616061 | ||||||
| chr19:1616070
|
G | A | 3 | a0001c0003t0002g0245a0001c0003t0032g0237a0001c0007t0091g0300 | 3 | HG00438.hp1 NA18952.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1451-249C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616070 | ||||||
| chr19:1616070
|
G | C | 1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1451-249C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616070 | ||||||
| chr19:1616079
|
C | T | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451-258G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616079 | ||||||
| chr19:1616123
|
T | C | 1 | a0001c0003t0002g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1451-302A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616123 | ||||||
| chr19:1616342
|
T | C | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451-521A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616342 | ||||||
| chr19:1616431
|
G | A | 1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1451-610C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616431 | ||||||
| chr19:1616449
|
G | A | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1451-628C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616449 | ||||||
| chr19:1616469
|
G | A | 1 | a0002c0001t0007g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1451-648C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616469 | ||||||
| chr19:1616473
|
CA | C | 8 | a0001c0004t0002g0257a0001c0004t0003g0099a0001c0004t0008g0256others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1451-653delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616473 | ||||||
| chr19:1616488
|
G | A | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1451-667C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616488 | ||||||
| chr19:1616625
|
G | A | 1 | a0001c0002t0002g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1451-804C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616625 | ||||||
| chr19:1616645
|
G | A | 38 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0003t0005g0331others(35): Show | 38 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1451-824C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616645 | ||||||
| chr19:1616702
|
G | A | 1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1451-881C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616702 | ||||||
| chr19:1616771
|
A | G | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1451-950T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616771 | ||||||
| chr19:1616889
|
C | T | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451-1068G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616889 | ||||||
| chr19:1616946
|
AAAAG | A | 4 | a0001c0003t0001g0261a0001c0003t0005g0336a0001c0007t0002g0049others(1): Show | 4 | HG01943.hp1 HG01952.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1451-1129_1451-112 others(8): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616946 | ||||||
| chr19:1616990
|
G | C | 1 | a0001c0002t0002g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1451-1169C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1616990 | ||||||
| chr19:1617012
|
C | G | 1 | a0001c0002t0002g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1451-1191G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617012 | ||||||
| chr19:1617038
|
C | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1451-1217G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617038 | ||||||
| chr19:1617171
|
C | T | 2 | a0001c0005t0004g0010a0001c0005t0025g0034 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1451-1350G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617171 | ||||||
| chr19:1617281
|
G | A | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1451-1460C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617281 | ||||||
| chr19:1617297
|
A | C | 1 | a0003c0006t0033g0315 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1451-1476T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617297 | ||||||
| chr19:1617299
|
G | A | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1451-1478C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617299 | ||||||
| chr19:1617374
|
G | A | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1451-1553C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617374 | ||||||
| chr19:1617463
|
A | G | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1451-1642T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617463 | ||||||
| chr19:1617515
|
C | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1450+1596G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617515 | ||||||
| chr19:1617602
|
C | G | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+1509G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617602 | ||||||
| chr19:1617636
|
T | C | 3 | a0001c0004t0001g0166a0001c0004t0002g0257a0001c0004t0086g0303 | 3 | HG01361.hp2 HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1450+1475A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617636 | ||||||
| chr19:1617766
|
A | G | 1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1450+1345T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617766 | ||||||
| chr19:1617821
|
C | G | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1450+1290G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617821 | ||||||
| chr19:1617825
|
G | A | 1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1450+1286C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617825 | ||||||
| chr19:1617835
|
T | C | 1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1450+1276A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617835 | ||||||
| chr19:1617954
|
A | G | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450+1157T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1617954 | ||||||
| chr19:1618087
|
C | T | 3 | a0001c0004t0001g0110a0001c0004t0002g0108a0001c0004t0002g0154 | 3 | HG02109.hp1 HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1450+1024G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618087 | ||||||
| chr19:1618090
|
TCAA | T | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+1018_1450+102 others(7): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618090 | ||||||
| chr19:1618324
|
C | T | 1 | a0001c0003t0005g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1450+787G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618324 | ||||||
| chr19:1618379
|
G | A | 1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1450+732C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618379 | ||||||
| chr19:1618489
|
T | A | 2 | a0001c0013t0037g0009a0001c0013t0042g0033 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1450+622A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618489 | ||||||
| chr19:1618504
|
C | T | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450+607G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618504 | ||||||
| chr19:1618505
|
G | A | 2 | a0001c0004t0011g0102a0001c0004t0028g0101 | 2 | NA18944.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1450+606C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618505 | ||||||
| chr19:1618514
|
C | G | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1450+597G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618514 | ||||||
| chr19:1618515
|
C | G | 1 | a0001c0004t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1450+596G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618515 | ||||||
| chr19:1618545
|
C | T | 3 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0032g0161 | 3 | HG02257.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1450+566G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618545 | ||||||
| chr19:1618553
|
C | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1450+558G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618553 | ||||||
| chr19:1618638
|
C | T | 1 | a0001c0007t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1450+473G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618638 | ||||||
| chr19:1618719
|
C | T | 1 | a0002c0001t0064g0053 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1450+392G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618719 | ||||||
| chr19:1618741
|
C | T | 4 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450+370G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618741 | ||||||
| chr19:1618776
|
C | G | 1 | a0002c0001t0006g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1450+335G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618776 | ||||||
| chr19:1618787
|
G | A | 2 | a0001c0007t0020g0289a0003c0011t0030g0139 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1450+324C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618787 | ||||||
| chr19:1618835
|
G | A | 1 | a0001c0005t0045g0040 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1450+276C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618835 | ||||||
| chr19:1618835
|
G | GCC | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450+274_1450+275d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618835 | ||||||
| chr19:1618853
|
A | G | 1 | a0001c0019t0026g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1450+258T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618853 | ||||||
| chr19:1618909
|
T | C | 5 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450+202A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618909 | ||||||
| chr19:1618938
|
C | T | 1 | a0002c0001t0064g0053 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1450+173G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1618938 | ||||||
| chr19:1619011
|
G | GACC | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0169others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450+99_1450+100in others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 16/18 | chr19 | 1619011 | ||||||
| chr19:1619309
|
C | A | 6 | a0001c0007t0002g0127a0001c0007t0012g0323a0002c0001t0029g0156others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG02071.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1326+7G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 15/18 | chr19 | 1619309 | ||||||
| chr19:1619600
|
G | A | 1 | a0003c0006t0002g0114 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1168-126C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619600 | ||||||
| chr19:1619723
|
C | A | 1 | a0001c0005t0023g0015 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1167+57G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619723 | ||||||
| chr19:1619745
|
G | A | 1 | a0001c0005t0039g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1167+35C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619745 | ||||||
| chr19:1619750
|
A | AGGGTG | 151 | a0001c0002t0001g0181a0001c0002t0013g0197a0001c0002t0027g0196others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1167+25_1167+29dup others(5): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619750 | ||||||
| chr19:1619750
|
A | AGGGTGGG others(3): Show |
9 | a0001c0004t0001g0110a0001c0004t0002g0108a0001c0004t0002g0154others(6): Show | 9 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1167+20_1167+29dup others(10): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619750 | ||||||
| chr19:1619758
|
G | C | 6 | a0001c0002t0001g0174a0001c0002t0001g0203a0001c0002t0002g0175others(3): Show | 6 | HG01106.hp2 HG01884.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1167+22C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619758 | ||||||
| chr19:1619768
|
G | T | 1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1167+12C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619768 | ||||||
| chr19:1619770
|
A | C | 1 | a0001c0002t0065g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1167+10T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 14/18 | chr19 | 1619770 | ||||||
| chr19:1619885
|
G | A | 3 | a0005c0010t0018g0169a0005c0010t0018g0170a0005c0010t0018g0171 | 3 | HG01884.hp2 HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1094-32C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1619885 | ||||||
| chr19:1619910
|
G | A | 2 | a0001c0007t0071g0199a0015c0024t0072g0179 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1094-57C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1619910 | ||||||
| chr19:1619958
|
G | A | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1094-105C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1619958 | ||||||
| chr19:1619981
|
C | T | 2 | a0001c0005t0027g0193a0003c0008t0082g0299 | 2 | HG03130.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1094-128G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1619981 | ||||||
| chr19:1620002
|
A | G | 2 | a0001c0007t0071g0199a0015c0024t0072g0179 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1094-149T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620002 | ||||||
| chr19:1620179
|
G | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1094-326C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620179 | ||||||
| chr19:1620198
|
C | T | 2 | a0001c0007t0071g0199a0015c0024t0072g0179 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1094-345G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620198 | ||||||
| chr19:1620202
|
A | G | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1094-349T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620202 | ||||||
| chr19:1620328
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1094-475C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620328 | ||||||
| chr19:1620370
|
C | T | 2 | a0001c0004t0003g0249a0001c0004t0008g0250 | 2 | HG00099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1094-517G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620370 | ||||||
| chr19:1620396
|
G | A | 10 | a0001c0004t0003g0246a0001c0004t0003g0249a0001c0004t0003g0286others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1094-543C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620396 | ||||||
| chr19:1620435
|
G | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1093+533C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620435 | ||||||
| chr19:1620494
|
A | T | 1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1093+474T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620494 | ||||||
| chr19:1620498
|
T | C | 2 | a0001c0003t0001g0234a0001c0003t0005g0340 | 2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1093+470A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620498 | ||||||
| chr19:1620537
|
G | A | 13 | a0001c0003t0076g0045a0001c0004t0001g0110a0001c0004t0002g0108others(10): Show | 13 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1093+431C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620537 | ||||||
| chr19:1620741
|
T | C | 1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1093+227A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620741 | ||||||
| chr19:1620830
|
G | C | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0004c0033t0036g0350others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093+138C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620830 | ||||||
| chr19:1620867
|
C | A | 2 | a0001c0013t0037g0009a0001c0013t0042g0033 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1093+101G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620867 | ||||||
| chr19:1620883
|
C | T | 1 | a0001c0005t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1093+85G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620883 | ||||||
| chr19:1620884
|
G | C | 3 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0032g0161 | 3 | HG02257.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1093+84C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620884 | ||||||
| chr19:1620919
|
C | G | 1 | a0001c0004t0099g0343 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1093+49G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620919 | ||||||
| chr19:1620951
|
C | T | 1 | a0001c0004t0066g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1093+17G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 13/18 | chr19 | 1620951 | ||||||
| chr19:1621113
|
C | T | 1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1014+20G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 12/18 | chr19 | 1621113 | ||||||
| chr19:1621228
|
C | A | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.956-37G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621228 | ||||||
| chr19:1621236
|
C | T | 1 | a0002c0001t0006g0074 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.956-45G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621236 | ||||||
| chr19:1621247
|
G | A | 1 | a0003c0006t0012g0313 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.956-56C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621247 | ||||||
| chr19:1621262
|
G | A | 1 | a0001c0004t0002g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.956-71C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621262 | ||||||
| chr19:1621291
|
G | A | 12 | a0001c0004t0003g0153a0001c0004t0008g0103a0001c0004t0008g0151others(9): Show | 12 | HG00408.hp2 HG00597.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.956-100C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621291 | ||||||
| chr19:1621450
|
T | C | 68 | a0001c0007t0001g0217a0001c0007t0002g0049a0001c0007t0002g0127others(65): Show | 68 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.956-259A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621450 | ||||||
| chr19:1621462
|
T | C | 4 | a0001c0002t0001g0180a0001c0002t0001g0265a0001c0002t0002g0264others(1): Show | 4 | HG02451.hp2 NA18970.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-271A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621462 | ||||||
| chr19:1621479
|
CTGAGTCC others(19): Show |
C | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.956-314_956-289del others(26): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621479 | ||||||
| chr19:1621500
|
G | C | 1 | a0002c0001t0007g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.956-309C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621500 | ||||||
| chr19:1621521
|
G | GCCTGGGT others(19): Show |
14 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0213others(11): Show | 14 | HG01081.hp1 HG01256.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.955+291_955+316dup others(26): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621521 | ||||||
| chr19:1621521
|
G | GCCTGGGT others(45): Show |
2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.955+265_955+316dup others(52): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621521 | ||||||
| chr19:1621521
|
GCCTGGGT others(19): Show |
G | 1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.955+291_955+316del others(26): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621521 | ||||||
| chr19:1621629
|
C | T | 1 | a0001c0007t0012g0323 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.955+209G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621629 | ||||||
| chr19:1621631
|
C | A | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.955+207G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621631 | ||||||
| chr19:1621662
|
G | A | 7 | a0001c0003t0001g0200a0001c0003t0001g0201a0001c0003t0001g0255others(4): Show | 7 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.955+176C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621662 | ||||||
| chr19:1621673
|
G | A | 1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.955+165C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621673 | ||||||
| chr19:1621767
|
A | AC | 11 | a0001c0002t0002g0272a0001c0003t0005g0332a0001c0005t0004g0017others(8): Show | 11 | HG00597.hp2 HG02056.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.955+70dupG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 11/18 | chr19 | 1621767 | ||||||
| chr19:1621983
|
G | A | 1 | a0002c0001t0006g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.823-13C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 10/18 | chr19 | 1621983 | ||||||
| chr19:1622297
|
C | A | 4 | a0002c0001t0029g0156a0002c0001t0029g0159a0002c0001t0054g0157others(1): Show | 4 | HG00738.hp1 HG01069.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+16G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 9/18 | chr19 | 1622297 | ||||||
| chr19:1622459
|
A | G | 6 | a0004c0014t0013g0288a0004c0014t0079g0305a0004c0033t0036g0350others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.550-44T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1622459 | ||||||
| chr19:1622561
|
T | A | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.550-146A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1622561 | ||||||
| chr19:1622672
|
G | A | 2 | a0001c0002t0013g0182a0002c0001t0092g0295 | 2 | HG02723.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.550-257C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1622672 | ||||||
| chr19:1622675
|
T | C | 1 | a0001c0003t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.550-260A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1622675 | ||||||
| chr19:1622785
|
C | T | 62 | a0001c0007t0001g0217a0001c0007t0002g0049a0001c0007t0002g0282others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.550-370G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1622785 | ||||||
| chr19:1623014
|
G | C | 1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.550-599C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623014 | ||||||
| chr19:1623150
|
T | C | 1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-735A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623150 | ||||||
| chr19:1623168
|
G | C | 1 | a0001c0003t0002g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.550-753C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623168 | ||||||
| chr19:1623221
|
G | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+730C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623221 | ||||||
| chr19:1623266
|
G | A | 7 | a0001c0003t0001g0200a0001c0003t0001g0201a0001c0003t0001g0255others(4): Show | 7 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+685C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623266 | ||||||
| chr19:1623382
|
C | CT | 95 | a0001c0002t0001g0111a0001c0002t0001g0180a0001c0002t0001g0209others(92): Show | 95 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.549+568dupA | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623382 | ||||||
| chr19:1623382
|
C | CTT | 9 | a0001c0007t0002g0282a0002c0001t0006g0067a0002c0001t0006g0075others(6): Show | 9 | HG00738.hp1 HG02523.hp2 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.549+567_549+568dup others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623382 | ||||||
| chr19:1623382
|
CT | C | 9 | a0001c0002t0002g0048a0001c0004t0003g0105a0001c0004t0003g0280others(6): Show | 9 | HG01255.hp2 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+568delA | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623382 | ||||||
| chr19:1623382
|
CTT | C | 7 | a0001c0004t0001g0110a0001c0004t0002g0108a0001c0004t0002g0154others(4): Show | 7 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+567_549+568del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623382 | ||||||
| chr19:1623441
|
C | T | 2 | a0003c0008t0082g0299a0003c0008t0101g0346 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.549+510G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623441 | ||||||
| chr19:1623469
|
C | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.549+482G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623469 | ||||||
| chr19:1623576
|
G | A | 2 | a0001c0004t0011g0102a0001c0004t0028g0101 | 2 | NA18944.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.549+375C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623576 | ||||||
| chr19:1623687
|
T | C | 3 | a0001c0003t0005g0326a0001c0003t0077g0241a0001c0007t0001g0238 | 3 | HG01074.hp2 HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.549+264A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623687 | ||||||
| chr19:1623816
|
C | A | 1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.549+135G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623816 | ||||||
| chr19:1623851
|
G | C | 62 | a0001c0007t0001g0217a0001c0007t0002g0049a0001c0007t0002g0282others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.549+100C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623851 | ||||||
| chr19:1623883
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+68G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 8/18 | chr19 | 1623883 | ||||||
| chr19:1624008
|
A | G | 155 | a0001c0003t0008g0098a0001c0003t0028g0144a0001c0003t0059g0187others(152): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
splice_region_variant&intron_variant | LOW | c.500-8T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624008 | ||||||
| chr19:1624037
|
C | A | 4 | a0001c0007t0020g0289a0003c0011t0030g0139a0006c0012t0020g0262others(1): Show | 4 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-37G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624037 | ||||||
| chr19:1624040
|
T | C | 1 | a0001c0003t0055g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.500-40A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624040 | ||||||
| chr19:1624089
|
C | T | 2 | a0001c0002t0001g0181a0001c0002t0002g0186 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.500-89G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624089 | ||||||
| chr19:1624146
|
C | A | 3 | a0001c0004t0003g0099a0001c0004t0008g0097a0001c0004t0008g0100 | 3 | HG00639.hp1 HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.500-146G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624146 | ||||||
| chr19:1624264
|
C | T | 115 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(112): Show | 115 | HG00609.hp1 HG00673.hp2 HG01069.hp1 others(112): Show |
intron_variant | MODIFIER | c.500-264G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624264 | ||||||
| chr19:1624333
|
C | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.500-333G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624333 | ||||||
| chr19:1624344
|
C | T | 2 | a0003c0011t0030g0139a0015c0024t0072g0179 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.500-344G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624344 | ||||||
| chr19:1624412
|
G | A | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.500-412C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624412 | ||||||
| chr19:1624415
|
G | A | 1 | a0001c0002t0046g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500-415C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624415 | ||||||
| chr19:1624491
|
G | A | 1 | a0002c0001t0006g0086 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.500-491C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624491 | ||||||
| chr19:1624528
|
A | G | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.500-528T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624528 | ||||||
| chr19:1624619
|
C | A | 1 | a0001c0002t0083g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.500-619G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624619 | ||||||
| chr19:1624678
|
C | G | 3 | a0002c0001t0006g0055a0002c0001t0006g0089a0002c0001t0019g0056 | 3 | NA18944.hp2 NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.500-678G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624678 | ||||||
| chr19:1624679
|
G | A | 1 | a0001c0005t0045g0040 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.500-679C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624679 | ||||||
| chr19:1624705
|
G | A | 1 | a0021c0015t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.500-705C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624705 | ||||||
| chr19:1624766
|
C | G | 40 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(37): Show | 40 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.500-766G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624766 | ||||||
| chr19:1624767
|
T | G | 40 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(37): Show | 40 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.500-767A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624767 | ||||||
| chr19:1624852
|
G | A | 5 | a0001c0002t0001g0178a0001c0002t0001g0198a0001c0002t0002g0267others(2): Show | 5 | HG01192.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+724C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624852 | ||||||
| chr19:1624924
|
C | T | 1 | a0001c0002t0005g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.499+652G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624924 | ||||||
| chr19:1624997
|
C | T | 3 | a0001c0003t0005g0326a0001c0003t0077g0241a0001c0007t0001g0238 | 3 | HG01074.hp2 HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.499+579G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1624997 | ||||||
| chr19:1625021
|
A | C | 1 | a0001c0003t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.499+555T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625021 | ||||||
| chr19:1625038
|
G | A | 1 | a0002c0001t0007g0060 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.499+538C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625038 | ||||||
| chr19:1625039
|
A | T | 1 | a0002c0001t0007g0060 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.499+537T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625039 | ||||||
| chr19:1625218
|
G | A | 1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.499+358C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625218 | ||||||
| chr19:1625384
|
C | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.499+192G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625384 | ||||||
| chr19:1625437
|
C | T | 4 | a0001c0005t0009g0016a0001c0005t0023g0015a0001c0005t0038g0025others(1): Show | 4 | NA18962.hp2 NA18990.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+139G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625437 | ||||||
| chr19:1625438
|
G | A | 1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.499+138C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625438 | ||||||
| chr19:1625559
|
G | A | 44 | a0001c0002t0001g0078a0001c0002t0001g0180a0001c0002t0001g0209others(41): Show | 44 | HG00609.hp1 HG01081.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.499+17C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 7/18 | chr19 | 1625559 | ||||||
| chr19:1625812
|
T | C | 160 | a0001c0002t0002g0188a0001c0003t0001g0096a0001c0003t0002g0094others(157): Show | 160 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.367-104A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1625812 | ||||||
| chr19:1625813
|
G | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.367-105C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1625813 | ||||||
| chr19:1625912
|
A | C | 1 | a0001c0004t0008g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.367-204T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1625912 | ||||||
| chr19:1625921
|
G | A | 1 | a0001c0005t0004g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.367-213C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1625921 | ||||||
| chr19:1625984
|
G | A | 2 | a0001c0002t0001g0078a0001c0002t0002g0143 | 2 | HG02015.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.367-276C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1625984 | ||||||
| chr19:1626095
|
G | T | 2 | a0001c0003t0001g0228a0001c0003t0002g0274 | 2 | HG00639.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.367-387C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626095 | ||||||
| chr19:1626143
|
T | C | 2 | a0001c0007t0074g0090a0001c0007t0096g0311 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.367-435A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626143 | ||||||
| chr19:1626172
|
C | T | 3 | a0002c0001t0015g0080a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01358.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.367-464G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626172 | ||||||
| chr19:1626182
|
G | A | 1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.367-474C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626182 | ||||||
| chr19:1626259
|
T | C | 1 | a0001c0005t0009g0022 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.367-551A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626259 | ||||||
| chr19:1626318
|
C | T | 1 | a0018c0018t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.367-610G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626318 | ||||||
| chr19:1626382
|
A | T | 1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.367-674T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626382 | ||||||
| chr19:1626406
|
C | T | 1 | a0001c0003t0005g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.367-698G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626406 | ||||||
| chr19:1626435
|
C | G | 2 | a0001c0013t0037g0009a0001c0013t0042g0033 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.367-727G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626435 | ||||||
| chr19:1626448
|
CA | C | 6 | a0001c0003t0002g0247a0001c0005t0044g0041a0001c0007t0003g0107others(3): Show | 6 | HG01943.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-741delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626448 | ||||||
| chr19:1626457
|
A | G | 3 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0002t0078g0189 | 3 | HG02886.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.367-749T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626457 | ||||||
| chr19:1626477
|
A | G | 2 | a0001c0004t0011g0102a0001c0004t0028g0101 | 2 | NA18944.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.367-769T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626477 | ||||||
| chr19:1626555
|
C | T | 2 | a0001c0013t0037g0009a0001c0013t0042g0033 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.366+804G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626555 | ||||||
| chr19:1626702
|
C | T | 1 | a0001c0004t0003g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.366+657G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626702 | ||||||
| chr19:1626758
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.366+601G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626758 | ||||||
| chr19:1626869
|
C | T | 1 | a0009c0021t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.366+490G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1626869 | ||||||
| chr19:1627016
|
G | C | 1 | a0006c0012t0020g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.366+343C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1627016 | ||||||
| chr19:1627026
|
G | A | 1 | a0001c0003t0032g0237 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.366+333C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1627026 | ||||||
| chr19:1627076
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.366+283C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1627076 | ||||||
| chr19:1627116
|
A | G | 1 | a0001c0005t0009g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.366+243T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 6/18 | chr19 | 1627116 | ||||||
| chr19:1627539
|
A | C | 1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-113T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627539 | ||||||
| chr19:1627556
|
C | T | 2 | a0004c0014t0013g0288a0004c0014t0079g0305 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.299-130G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627556 | ||||||
| chr19:1627577
|
GTGCCCAT others(23): Show |
G | 3 | a0002c0001t0007g0065a0002c0001t0019g0084a0013c0022t0007g0066 | 3 | NA19000.hp1 NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.299-181_299-152del others(30): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627577 | ||||||
| chr19:1627594
|
C | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-168G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627594 | ||||||
| chr19:1627598
|
G | A | 3 | a0001c0002t0001g0111a0001c0002t0005g0319a0001c0004t0066g0172 | 3 | HG02145.hp1 HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.299-172C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627598 | ||||||
| chr19:1627620
|
G | A | 1 | a0001c0002t0013g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.299-194C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627620 | ||||||
| chr19:1627631
|
C | A | 1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.299-205G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627631 | ||||||
| chr19:1627747
|
G | A | 1 | a0001c0002t0078g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-321C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627747 | ||||||
| chr19:1627750
|
C | T | 2 | a0003c0006t0001g0148a0003c0008t0001g0118 | 2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.299-324G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627750 | ||||||
| chr19:1627753
|
A | AAAGGGGA others(129): Show |
1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.299-328_299-327ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627753 | ||||||
| chr19:1627753
|
A | AAAGGGGA others(26): Show |
1 | a0001c0004t0021g0334 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.299-360_299-328dup others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627753 | ||||||
| chr19:1627753
|
A | AAAGGGGA others(96): Show |
1 | a0001c0007t0090g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.299-430_299-328dup others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627753 | ||||||
| chr19:1627753
|
A | G | 1 | a0001c0002t0078g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-327T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627753 | ||||||
| chr19:1627753
|
AAAGGGGA others(1157): Show |
A | 2 | a0002c0001t0006g0074a0002c0001t0006g0086 | 2 | HG00558.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.299-1491_299-328de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627753 | ||||||
| chr19:1627777
|
G | A | 1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.299-351C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627777 | ||||||
| chr19:1627780
|
A | G | 1 | a0001c0007t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.299-354T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627780 | ||||||
| chr19:1627781
|
G | T | 1 | a0001c0005t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.299-355C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627781 | ||||||
| chr19:1627783
|
T | C | 14 | a0001c0002t0002g0186a0001c0002t0078g0189a0001c0003t0002g0229others(11): Show | 14 | HG00323.hp1 HG02071.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-357A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627783 | ||||||
| chr19:1627783
|
T | TGGGAAGG others(28): Show |
1 | a0001c0003t0001g0233 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.299-392_299-358dup others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627783 | ||||||
| chr19:1627783
|
T | TGGGAAGG others(130): Show |
1 | a0001c0003t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.299-358_299-357ins others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627783 | ||||||
| chr19:1627783
|
TGGGAAGG others(63): Show |
T | 3 | a0001c0005t0052g0205a0001c0009t0001g0177a0001c0009t0049g0167 | 3 | HG02615.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299-427_299-358del others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627783 | ||||||
| chr19:1627784
|
G | GGGAAGGG others(62): Show |
1 | a0001c0004t0002g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-359_299-358ins others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627784 | ||||||
| chr19:1627789
|
G | A | 1 | a0001c0007t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.299-363C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627789 | ||||||
| chr19:1627796
|
G | GCAGAACT others(27): Show |
2 | a0004c0033t0036g0350a0005c0010t0018g0169 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299-371_299-370ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627796 | ||||||
| chr19:1627797
|
C | T | 1 | a0002c0001t0070g0121 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.299-371G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627797 | ||||||
| chr19:1627801
|
G | A | 2 | a0003c0011t0030g0139a0005c0010t0018g0170 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.299-375C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627801 | ||||||
| chr19:1627805
|
A | ACGGGGGG others(230): Show |
1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-380_299-379ins others(237): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627805 | ||||||
| chr19:1627805
|
A | ACGGGGGG others(1107): Show |
1 | a0001c0002t0036g0348 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-380_299-379ins others(1114): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627805 | ||||||
| chr19:1627805
|
A | ACGGGGGT others(327): Show |
1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-380_299-379ins others(334): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627805 | ||||||
| chr19:1627805
|
A | G | 1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-379T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627805 | ||||||
| chr19:1627806
|
CAG | C | 3 | a0001c0007t0103g0351a0003c0008t0068g0268a0021c0015t0001g0231 | 3 | HG00323.hp1 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.299-382_299-381del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627806 | ||||||
| chr19:1627807
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-381T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627807 | ||||||
| chr19:1627807
|
AGGGGGTG others(270): Show |
A | 1 | a0001c0009t0098g0347 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.299-658_299-382del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627807 | ||||||
| chr19:1627808
|
G | C | 3 | a0001c0002t0002g0175a0001c0002t0036g0348a0003c0011t0030g0139 | 3 | HG01884.hp1 HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.299-382C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627808 | ||||||
| chr19:1627808
|
G | GGGGGTGA others(261): Show |
1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-383_299-382ins others(268): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627808 | ||||||
| chr19:1627808
|
G | GGGGGTGA others(128): Show |
1 | a0001c0007t0031g0239 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.299-383_299-382ins others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627808 | ||||||
| chr19:1627808
|
G | GGGGGTGA others(96): Show |
1 | a0001c0003t0005g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-383_299-382ins others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627808 | ||||||
| chr19:1627808
|
G | GGGGGTGA others(229): Show |
1 | a0001c0004t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.299-383_299-382ins others(236): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627808 | ||||||
| chr19:1627808
|
G | GGGGGTGG others(94): Show |
1 | a0001c0002t0002g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.299-383_299-382ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627808 | ||||||
| chr19:1627812
|
G | A | 3 | a0001c0002t0078g0189a0001c0003t0002g0229a0001c0007t0002g0149 | 3 | HG02300.hp1 HG02886.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.299-386C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627812 | ||||||
| chr19:1627815
|
A | G | 1 | a0005c0010t0018g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-389T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627815 | ||||||
| chr19:1627818
|
C | CGGGAAGG others(26): Show |
1 | a0002c0001t0007g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.299-393_299-392ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627818 | ||||||
| chr19:1627818
|
C | CGGGAAGG others(61): Show |
4 | a0001c0003t0008g0098a0001c0004t0003g0099a0001c0004t0008g0097others(1): Show | 4 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-393_299-392ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627818 | ||||||
| chr19:1627818
|
C | CGGGAAGG others(130): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-393_299-392ins others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627818 | ||||||
| chr19:1627818
|
C | CGGGAAGG others(61): Show |
1 | a0001c0005t0009g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.299-393_299-392ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627818 | ||||||
| chr19:1627818
|
C | CGGGAAGG others(63): Show |
6 | a0001c0005t0004g0011a0001c0005t0004g0023a0001c0005t0004g0028others(3): Show | 6 | HG01167.hp1 HG01361.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-393_299-392ins others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627818 | ||||||
| chr19:1627818
|
C | CGGGAAGG others(164): Show |
1 | a0001c0003t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.299-393_299-392ins others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627818 | ||||||
| chr19:1627818
|
C | CGGGAAGG others(66): Show |
1 | a0001c0005t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.299-393_299-392ins others(73): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627818 | ||||||
| chr19:1627824
|
G | A | 3 | a0004c0014t0013g0288a0004c0014t0079g0305a0005c0010t0018g0171 | 3 | HG02451.hp1 HG02559.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.299-398C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627824 | ||||||
| chr19:1627831
|
G | C | 1 | a0005c0010t0018g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-405C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627831 | ||||||
| chr19:1627836
|
G | A | 3 | a0001c0002t0002g0202a0001c0009t0050g0168a0002c0001t0019g0284 | 3 | HG02056.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299-410C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627836 | ||||||
| chr19:1627840
|
A | ACGGGGGT others(93): Show |
2 | a0003c0006t0001g0125a0017c0026t0002g0112 | 2 | HG00423.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.299-415_299-414ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627840 | ||||||
| chr19:1627840
|
A | ACGGGGGT others(194): Show |
1 | a0003c0006t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.299-415_299-414ins others(201): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627840 | ||||||
| chr19:1627840
|
A | ACGGGGGT others(262): Show |
1 | a0003c0008t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-415_299-414ins others(269): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627840 | ||||||
| chr19:1627840
|
A | ACGGGGTG others(91): Show |
1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-415_299-414ins others(98): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627840 | ||||||
| chr19:1627841
|
C | CGGGGTGA others(403): Show |
1 | a0001c0003t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-416_299-415ins others(410): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627841 | ||||||
| chr19:1627841
|
CA | C | 36 | a0001c0003t0055g0235a0001c0003t0059g0187a0001c0004t0003g0286others(33): Show | 36 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.299-416delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627841 | ||||||
| chr19:1627841
|
CAG | C | 25 | a0001c0002t0002g0202a0001c0002t0002g0210a0001c0003t0001g0152others(22): Show | 26 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-417_299-416del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627841 | ||||||
| chr19:1627842
|
A | AGGGGATG others(60): Show |
1 | a0001c0002t0078g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-417_299-416ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627842 | ||||||
| chr19:1627842
|
A | AGGGGGTG others(27): Show |
1 | a0001c0003t0005g0325 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.299-450_299-417dup others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627842 | ||||||
| chr19:1627842
|
A | AGGGGGTG others(229): Show |
1 | a0001c0005t0017g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.299-417_299-416ins others(236): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627842 | ||||||
| chr19:1627842
|
A | AGGGGGTG others(27): Show |
1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-417_299-416ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627842 | ||||||
| chr19:1627842
|
A | C | 1 | a0001c0003t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-416T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627842 | ||||||
| chr19:1627842
|
A | G | 2 | a0001c0002t0036g0348a0003c0011t0030g0139 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.299-416T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627842 | ||||||
| chr19:1627843
|
G | C | 5 | a0001c0005t0002g0131a0003c0006t0001g0115a0003c0006t0001g0125others(2): Show | 5 | HG00423.hp2 HG03704.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-417C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627843 | ||||||
| chr19:1627843
|
G | GGGGATGA others(26): Show |
8 | a0001c0004t0003g0044a0001c0004t0003g0105a0001c0004t0003g0106others(5): Show | 8 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-418_299-417ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627843 | ||||||
| chr19:1627843
|
G | GGGGGTGA others(500): Show |
1 | a0001c0002t0002g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-418_299-417ins others(507): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627843 | ||||||
| chr19:1627843
|
G | GGGGGTGA others(59): Show |
1 | a0001c0007t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.299-418_299-417ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627843 | ||||||
| chr19:1627843
|
G | GGGGGTGG others(129): Show |
1 | a0001c0003t0076g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-418_299-417ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627843 | ||||||
| chr19:1627847
|
G | A | 26 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0002g0133others(23): Show | 26 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.299-421C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627847 | ||||||
| chr19:1627847
|
G | GTGAGGCG others(298): Show |
1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-422_299-421ins others(305): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627847 | ||||||
| chr19:1627850
|
A | AGGCGGGA others(59): Show |
1 | a0001c0002t0035g0349 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299-425_299-424ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627850 | ||||||
| chr19:1627850
|
A | G | 5 | a0001c0002t0013g0197a0001c0007t0071g0199a0001c0007t0103g0351others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-424T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627850 | ||||||
| chr19:1627853
|
C | CGGGAAAG others(197): Show |
1 | a0001c0004t0011g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.299-428_299-427ins others(204): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627853 | ||||||
| chr19:1627853
|
C | CGGGAAGG others(26): Show |
4 | a0002c0001t0014g0073a0002c0001t0029g0159a0002c0001t0053g0057others(1): Show | 4 | HG00738.hp1 HG01069.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-428_299-427ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627853 | ||||||
| chr19:1627853
|
C | CGGGAAGG others(164): Show |
1 | a0001c0004t0086g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.299-428_299-427ins others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627853 | ||||||
| chr19:1627853
|
C | CGGGAAGG others(28): Show |
1 | a0001c0005t0023g0032 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.299-428_299-427ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627853 | ||||||
| chr19:1627853
|
C | CGGGAAGG others(26): Show |
1 | a0001c0005t0009g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.299-428_299-427ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627853 | ||||||
| chr19:1627853
|
C | T | 15 | a0001c0002t0001g0203a0001c0002t0002g0202a0001c0003t0002g0094others(12): Show | 15 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-427G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627853 | ||||||
| chr19:1627859
|
G | A | 18 | a0001c0004t0003g0153a0001c0004t0011g0134a0001c0004t0011g0136others(15): Show | 18 | HG01074.hp1 HG01257.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-433C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627859 | ||||||
| chr19:1627859
|
G | GGGGACAG others(59): Show |
1 | a0001c0007t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-434_299-433ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627859 | ||||||
| chr19:1627871
|
G | A | 16 | a0001c0002t0001g0173a0001c0002t0002g0267a0001c0002t0036g0348others(13): Show | 16 | HG00621.hp1 HG01192.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-445C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627871 | ||||||
| chr19:1627871
|
G | GCTCACGG others(200): Show |
1 | a0001c0005t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.299-446_299-445ins others(207): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627871 | ||||||
| chr19:1627875
|
A | ACGGGGGT others(94): Show |
1 | a0001c0007t0020g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.299-450_299-449ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627875 | ||||||
| chr19:1627875
|
A | ACGGGGGT others(25): Show |
1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.299-450_299-449ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627875 | ||||||
| chr19:1627875
|
A | ACGGGGTG others(24): Show |
1 | a0001c0007t0003g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-450_299-449ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627875 | ||||||
| chr19:1627875
|
A | ACGGGGTG others(58): Show |
1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-450_299-449ins others(65): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627875 | ||||||
| chr19:1627875
|
A | ACGGGGTG others(696): Show |
1 | a0002c0001t0007g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.299-450_299-449ins others(703): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627875 | ||||||
| chr19:1627875
|
A | ACGGGGTG others(57): Show |
2 | a0001c0003t0001g0200a0001c0003t0001g0201 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.299-450_299-449ins others(64): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627875 | ||||||
| chr19:1627875
|
A | G | 1 | a0004c0014t0079g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.299-449T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627875 | ||||||
| chr19:1627876
|
CA | C | 19 | a0001c0002t0001g0209a0001c0002t0001g0216a0001c0002t0002g0202others(16): Show | 19 | HG00099.hp1 HG00438.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-451delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627876 | ||||||
| chr19:1627876
|
CAG | C | 37 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0001g0180others(34): Show | 37 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.299-452_299-451del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627876 | ||||||
| chr19:1627877
|
A | AGGGGATG others(129): Show |
1 | a0001c0004t0081g0302 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.299-452_299-451ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627877 | ||||||
| chr19:1627877
|
A | AGGGGGTG others(27): Show |
1 | a0001c0004t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299-485_299-452dup others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627877 | ||||||
| chr19:1627877
|
A | G | 5 | a0001c0002t0001g0173a0001c0002t0001g0203a0001c0002t0002g0267others(2): Show | 5 | HG01192.hp1 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-451T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627877 | ||||||
| chr19:1627877
|
AGGGGGTG others(200): Show |
A | 5 | a0001c0002t0001g0271a0001c0002t0002g0270a0001c0003t0001g0226others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-658_299-452del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627877 | ||||||
| chr19:1627878
|
G | C | 7 | a0001c0002t0001g0181a0001c0003t0001g0200a0001c0003t0001g0201others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-452C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGATGA others(26): Show |
19 | a0001c0007t0002g0127a0001c0025t0010g0266a0002c0001t0001g0122others(16): Show | 19 | HG00544.hp2 HG00621.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-453_299-452ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGATGA others(59): Show |
2 | a0001c0002t0013g0182a0001c0005t0027g0193 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299-453_299-452ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGATGA others(395): Show |
1 | a0002c0001t0015g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-453_299-452ins others(402): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGATGA others(663): Show |
2 | a0002c0001t0006g0068a0002c0001t0088g0292 | 2 | HG00609.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.299-453_299-452ins others(670): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGATGA others(160): Show |
3 | a0001c0004t0003g0286a0001c0007t0012g0323a0003c0006t0002g0123 | 3 | HG02055.hp1 NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.299-453_299-452ins others(167): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGATGA others(261): Show |
1 | a0002c0001t0015g0080 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-453_299-452ins others(268): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGATGA others(26): Show |
2 | a0001c0002t0002g0191a0003c0006t0067g0130 | 2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.299-453_299-452ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGGTGA others(26): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-485_299-453dup others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGGTGA others(297): Show |
1 | a0001c0005t0009g0022 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.299-453_299-452ins others(304): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGGTGA others(59): Show |
1 | a0001c0005t0009g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.299-453_299-452ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGGTGA others(608): Show |
1 | a0001c0003t0089g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-453_299-452ins others(615): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
G | GGGGGTGA others(61): Show |
3 | a0001c0005t0023g0015a0001c0005t0038g0025a0001c0005t0039g0014 | 3 | NA18990.hp2 NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.299-453_299-452ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
GGGGGTGA others(268): Show |
G | 1 | a0003c0006t0001g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.299-727_299-453del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627878
|
GGGGGTGA others(953): Show |
G | 1 | a0001c0002t0027g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.299-1412_299-453de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627878 | ||||||
| chr19:1627882
|
G | A | 51 | a0001c0002t0002g0175a0001c0002t0002g0190a0001c0002t0078g0189others(48): Show | 51 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.299-456C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627882 | ||||||
| chr19:1627885
|
A | G | 5 | a0001c0003t0076g0045a0005c0010t0018g0170a0005c0010t0018g0171others(2): Show | 5 | HG01884.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-459T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627885 | ||||||
| chr19:1627888
|
C | CGGGAAGG others(61): Show |
1 | a0001c0004t0008g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-463_299-462ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627888 | ||||||
| chr19:1627888
|
C | T | 32 | a0001c0002t0001g0138a0001c0002t0078g0189a0001c0003t0008g0098others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.299-462G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627888 | ||||||
| chr19:1627894
|
G | A | 6 | a0001c0007t0074g0090a0001c0007t0096g0311a0002c0001t0100g0342others(3): Show | 6 | HG00423.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-468C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627894 | ||||||
| chr19:1627901
|
G | C | 1 | a0005c0010t0018g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-475C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627901 | ||||||
| chr19:1627902
|
C | CAGAACTC others(302): Show |
1 | a0001c0002t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299-477_299-476ins others(309): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627902 | ||||||
| chr19:1627902
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-476G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627902 | ||||||
| chr19:1627906
|
G | A | 65 | a0001c0002t0001g0111a0001c0002t0001g0173a0001c0002t0001g0174others(62): Show | 65 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.299-480C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627906 | ||||||
| chr19:1627910
|
A | ACGGGGGT others(60): Show |
1 | a0001c0002t0002g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.299-485_299-484ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627910 | ||||||
| chr19:1627910
|
A | ACGGGGGT others(127): Show |
1 | a0006c0012t0020g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.299-485_299-484ins others(134): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627910 | ||||||
| chr19:1627910
|
A | ACGGGGTG others(24): Show |
1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-485_299-484ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627910 | ||||||
| chr19:1627910
|
A | ACGGGGTG others(368): Show |
1 | a0001c0004t0011g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-485_299-484ins others(375): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627910 | ||||||
| chr19:1627910
|
A | ACGGGGTG others(24): Show |
1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.299-485_299-484ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627910 | ||||||
| chr19:1627911
|
C | CGGGGTGA others(59): Show |
2 | a0002c0001t0016g0052a0002c0001t0016g0269 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.299-486_299-485ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627911
|
C | CGGGGTGA others(159): Show |
1 | a0002c0001t0073g0079 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.299-486_299-485ins others(166): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627911
|
C | CGGGGTGA others(25): Show |
2 | a0001c0002t0001g0173a0001c0002t0093g0341 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.299-486_299-485ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627911
|
CA | C | 14 | a0001c0002t0001g0218a0001c0002t0002g0188a0001c0002t0083g0307others(11): Show | 14 | HG00621.hp1 HG01106.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-486delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627911
|
CAG | C | 76 | a0001c0002t0001g0181a0001c0002t0001g0203a0001c0002t0002g0190others(73): Show | 76 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.299-487_299-486del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627911
|
CAGGGGGT others(29): Show |
C | 1 | a0001c0013t0037g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.299-521_299-486del others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627911
|
CAGGGGGT others(98): Show |
C | 2 | a0001c0007t0103g0351a0006c0012t0020g0262 | 2 | HG02258.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.299-590_299-486del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627911
|
CAGGGGGT others(133): Show |
C | 1 | a0003c0008t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299-625_299-486del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627911 | ||||||
| chr19:1627912
|
A | AGGGGATG others(194): Show |
1 | a0001c0002t0004g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-487_299-486ins others(201): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627912 | ||||||
| chr19:1627912
|
A | C | 5 | a0001c0002t0001g0173a0001c0002t0093g0341a0002c0001t0016g0052others(2): Show | 5 | HG00642.hp2 HG01070.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-486T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627912 | ||||||
| chr19:1627912
|
A | G | 12 | a0001c0002t0001g0111a0001c0002t0001g0174a0001c0002t0001g0178others(9): Show | 12 | HG01106.hp2 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-486T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627912 | ||||||
| chr19:1627912
|
AG | A | 9 | a0001c0003t0001g0152a0001c0003t0001g0227a0001c0003t0001g0228others(6): Show | 10 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-487delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627912 | ||||||
| chr19:1627913
|
G | C | 5 | a0001c0002t0002g0186a0001c0004t0011g0134a0003c0006t0001g0148others(2): Show | 5 | HG02015.hp1 HG02486.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-487C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGATGA others(59): Show |
1 | a0001c0005t0009g0013 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.299-488_299-487ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGATGA others(92): Show |
1 | a0001c0005t0024g0002 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.299-488_299-487ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGATGA others(129): Show |
1 | a0001c0003t0002g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.299-488_299-487ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGATGA others(192): Show |
1 | a0001c0002t0002g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-488_299-487ins others(199): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGATGA others(233): Show |
1 | a0001c0003t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-488_299-487ins others(240): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGATGA others(506): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-488_299-487ins others(513): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGATGA others(431): Show |
1 | a0001c0002t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299-488_299-487ins others(438): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(27): Show |
2 | a0001c0002t0001g0218a0001c0002t0083g0307 | 2 | HG01981.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.299-488_299-487ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(162): Show |
2 | a0001c0004t0003g0279a0001c0004t0021g0321 | 2 | HG02148.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.299-488_299-487ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(193): Show |
1 | a0001c0003t0055g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.299-488_299-487ins others(200): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(294): Show |
2 | a0001c0002t0001g0178a0001c0002t0005g0330 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.299-488_299-487ins others(301): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(199): Show |
1 | a0001c0003t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.299-488_299-487ins others(206): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(61): Show |
9 | a0001c0002t0001g0213a0001c0002t0001g0215a0001c0002t0002g0214others(6): Show | 9 | HG00609.hp1 HG01081.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-488_299-487ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(363): Show |
1 | a0001c0002t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.299-488_299-487ins others(370): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
G | GGGGGTGA others(129): Show |
6 | a0001c0002t0001g0209a0001c0002t0001g0216a0001c0002t0002g0219others(3): Show | 6 | HG01256.hp1 HG01433.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-488_299-487ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
GGGGGTGA others(61): Show |
G | 1 | a0001c0004t0003g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.299-555_299-488del others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627913
|
GGGGGTGA others(918): Show |
G | 1 | a0021c0015t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.299-1412_299-488de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627913 | ||||||
| chr19:1627917
|
G | A | 24 | a0001c0002t0002g0048a0001c0002t0002g0175a0001c0002t0002g0267others(21): Show | 24 | HG00673.hp2 HG01071.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-491C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627917 | ||||||
| chr19:1627917
|
GTGAGGCG others(28): Show |
G | 2 | a0001c0004t0011g0102a0001c0005t0004g0019 | 2 | HG03017.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.299-526_299-492del others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627917 | ||||||
| chr19:1627917
|
GTGAGGCG others(782): Show |
G | 1 | a0001c0004t0062g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.299-1280_299-492de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627917 | ||||||
| chr19:1627919
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.299-493C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627919 | ||||||
| chr19:1627919
|
G | GAGGCGGG others(164): Show |
5 | a0001c0002t0001g0212a0001c0002t0001g0265a0001c0002t0002g0264others(2): Show | 5 | HG02027.hp1 NA18970.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-494_299-493ins others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627919 | ||||||
| chr19:1627920
|
A | AGGCGGGA others(468): Show |
1 | a0001c0004t0003g0109 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.299-495_299-494ins others(475): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627920 | ||||||
| chr19:1627920
|
A | G | 13 | a0001c0003t0001g0152a0001c0003t0001g0227a0001c0003t0001g0228others(10): Show | 14 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-494T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627920 | ||||||
| chr19:1627923
|
C | CGGGAAGG others(94): Show |
3 | a0001c0004t0003g0153a0001c0004t0011g0136a0001c0004t0011g0137 | 3 | HG01074.hp1 HG01257.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.299-498_299-497ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627923 | ||||||
| chr19:1627923
|
C | CGGGAAGG others(26): Show |
1 | a0002c0001t0006g0075 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.299-498_299-497ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627923 | ||||||
| chr19:1627923
|
C | T | 6 | a0001c0002t0001g0203a0001c0003t0002g0095a0001c0004t0003g0091others(3): Show | 6 | HG00140.hp2 HG00741.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-497G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627923 | ||||||
| chr19:1627929
|
G | A | 9 | a0002c0001t0006g0055a0002c0001t0006g0076a0002c0001t0006g0089others(6): Show | 9 | HG00408.hp1 HG01358.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-503C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627929 | ||||||
| chr19:1627929
|
G | GGGGACAG others(162): Show |
1 | a0001c0002t0075g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-504_299-503ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627929 | ||||||
| chr19:1627929
|
G | GGGGACAG others(94): Show |
1 | a0003c0006t0010g0124 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.299-504_299-503ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627929 | ||||||
| chr19:1627937
|
C | CAGAACTC others(60): Show |
2 | a0001c0002t0005g0319a0012c0030t0002g0163 | 2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.299-512_299-511ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627937 | ||||||
| chr19:1627937
|
C | CAGAGCTC others(161): Show |
1 | a0001c0002t0085g0304 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.299-512_299-511ins others(168): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627937 | ||||||
| chr19:1627937
|
C | T | 2 | a0001c0002t0001g0173a0001c0002t0093g0341 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.299-511G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627937 | ||||||
| chr19:1627941
|
G | A | 29 | a0001c0002t0001g0111a0001c0002t0001g0198a0001c0002t0002g0184others(26): Show | 30 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.299-515C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627941 | ||||||
| chr19:1627945
|
A | ACGGGATG others(24): Show |
1 | a0001c0003t0002g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.299-520_299-519ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(625): Show |
1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-520_299-519ins others(632): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(197): Show |
1 | a0008c0032t0061g0211 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.299-520_299-519ins others(204): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(59): Show |
3 | a0002c0001t0006g0063a0002c0001t0007g0064a0002c0001t0069g0082 | 3 | NA19066.hp2 NA19068.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.299-520_299-519ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(327): Show |
2 | a0002c0001t0007g0085a0002c0001t0092g0295 | 2 | HG00673.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.299-520_299-519ins others(334): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(595): Show |
1 | a0002c0001t0064g0053 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.299-520_299-519ins others(602): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(829): Show |
1 | a0001c0007t0002g0049 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.299-520_299-519ins others(836): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(562): Show |
2 | a0002c0001t0007g0065a0013c0022t0007g0066 | 2 | NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.299-520_299-519ins others(569): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGGT others(124): Show |
3 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0032g0161 | 3 | HG02257.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.299-520_299-519ins others(131): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGTG others(59): Show |
2 | a0003c0006t0001g0092a0003c0006t0001g0116 | 2 | NA19056.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.299-520_299-519ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGTG others(92): Show |
1 | a0001c0004t0002g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-520_299-519ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGTG others(192): Show |
1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-520_299-519ins others(199): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGTG others(58): Show |
1 | a0001c0004t0021g0312 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.299-520_299-519ins others(65): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGTG others(193): Show |
1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.299-520_299-519ins others(200): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGTG others(360): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-520_299-519ins others(367): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627945
|
A | ACGGGGTG others(90): Show |
1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-520_299-519ins others(97): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627945 | ||||||
| chr19:1627946
|
C | CGGGGGTG others(294): Show |
1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299-521_299-520ins others(301): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627946 | ||||||
| chr19:1627946
|
C | CGGGGGTG others(294): Show |
1 | a0002c0001t0019g0084 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.299-521_299-520ins others(301): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627946 | ||||||
| chr19:1627946
|
C | CGGGGGTG others(59): Show |
1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-521_299-520ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627946 | ||||||
| chr19:1627946
|
CA | C | 47 | a0001c0002t0001g0203a0001c0002t0002g0143a0001c0002t0002g0191others(44): Show | 47 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.299-521delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627946 | ||||||
| chr19:1627946
|
CAG | C | 48 | a0001c0002t0001g0181a0001c0002t0002g0048a0001c0002t0002g0184others(45): Show | 49 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.299-522_299-521del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627946 | ||||||
| chr19:1627946
|
CAGGGGAT others(27): Show |
C | 1 | a0001c0009t0050g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-554_299-521del others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627946 | ||||||
| chr19:1627946
|
CAGGGGAT others(63): Show |
C | 1 | a0001c0002t0002g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.299-590_299-521del others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627946 | ||||||
| chr19:1627947
|
A | AGGGGGTG others(397): Show |
1 | a0002c0001t0087g0291 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.299-522_299-521ins others(404): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627947 | ||||||
| chr19:1627947
|
A | C | 3 | a0002c0001t0007g0070a0002c0001t0015g0155a0002c0001t0019g0084 | 3 | HG01978.hp1 NA18747.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.299-521T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627947 | ||||||
| chr19:1627947
|
A | G | 4 | a0001c0002t0013g0197a0001c0004t0003g0109a0001c0005t0001g0183others(1): Show | 4 | HG00423.hp1 HG01106.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-521T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627947 | ||||||
| chr19:1627948
|
G | C | 19 | a0001c0002t0001g0111a0001c0002t0001g0174a0001c0002t0001g0198others(16): Show | 19 | HG00673.hp1 HG01943.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.299-522C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627948 | ||||||
| chr19:1627948
|
G | GGGGGTGA others(96): Show |
2 | a0001c0005t0004g0027a0001c0005t0009g0021 | 2 | HG04115.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.299-523_299-522ins others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627948 | ||||||
| chr19:1627948
|
G | GGGGGTGA others(161): Show |
1 | a0001c0003t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.299-523_299-522ins others(168): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627948 | ||||||
| chr19:1627948
|
G | GGGGGTGA others(162): Show |
1 | a0001c0005t0023g0032 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.299-523_299-522ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627948 | ||||||
| chr19:1627948
|
G | T | 4 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0032g0161others(1): Show | 4 | HG02257.hp2 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-522C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627948 | ||||||
| chr19:1627952
|
A | G | 222 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0174others(219): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.299-526T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627952 | ||||||
| chr19:1627952
|
ATGAGGCG others(61): Show |
A | 1 | a0001c0007t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.299-594_299-527del others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627952 | ||||||
| chr19:1627954
|
G | A | 6 | a0001c0002t0001g0209a0001c0002t0001g0216a0001c0002t0002g0219others(3): Show | 6 | HG01256.hp1 HG01433.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-528C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627954 | ||||||
| chr19:1627955
|
A | AGGCGGGA others(94): Show |
1 | a0002c0001t0006g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.299-530_299-529ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627955 | ||||||
| chr19:1627955
|
A | G | 9 | a0001c0003t0028g0144a0001c0004t0081g0302a0001c0007t0074g0090others(6): Show | 9 | HG00621.hp1 HG02083.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-529T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627955 | ||||||
| chr19:1627956
|
G | A | 1 | a0001c0003t0028g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.299-530C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627956 | ||||||
| chr19:1627956
|
G | T | 1 | a0001c0007t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.299-530C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627956 | ||||||
| chr19:1627958
|
C | T | 10 | a0001c0002t0001g0198a0001c0002t0002g0184a0001c0002t0013g0197others(7): Show | 10 | HG00140.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-532G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627958 | ||||||
| chr19:1627964
|
G | A | 22 | a0001c0003t0059g0187a0001c0004t0003g0279a0001c0004t0021g0321others(19): Show | 22 | HG00544.hp2 HG00621.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-538C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627964 | ||||||
| chr19:1627972
|
C | T | 1 | a0002c0001t0070g0121 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.299-546G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627972 | ||||||
| chr19:1627976
|
G | A | 123 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(120): Show | 124 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.299-550C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627976 | ||||||
| chr19:1627981
|
C | CA | 6 | a0001c0002t0002g0143a0001c0003t0001g0234a0001c0003t0005g0338others(3): Show | 6 | HG00323.hp2 HG01175.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-556_299-555ins others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAG | 44 | a0001c0002t0001g0180a0001c0004t0003g0091a0001c0004t0003g0153others(41): Show | 44 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.299-556_299-555ins others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGAT others(768): Show |
1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.299-556_299-555ins others(775): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGAT others(432): Show |
3 | a0002c0001t0014g0058a0002c0001t0014g0059a0002c0001t0095g0317 | 3 | HG02523.hp2 NA18948.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.299-556_299-555ins others(439): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGAT others(634): Show |
1 | a0002c0001t0029g0156 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.299-556_299-555ins others(641): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(266): Show |
1 | a0003c0006t0080g0296 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.299-556_299-555ins others(273): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(165): Show |
1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-556_299-555ins others(172): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(132): Show |
1 | a0001c0002t0002g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-556_299-555ins others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(131): Show |
1 | a0001c0007t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.299-556_299-555ins others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(370): Show |
1 | a0001c0005t0004g0010 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299-556_299-555ins others(377): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(100): Show |
1 | a0001c0005t0009g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.299-556_299-555ins others(107): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(132): Show |
1 | a0002c0001t0029g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.299-556_299-555ins others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CAGGGGGT others(166): Show |
1 | a0001c0004t0011g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.299-556_299-555ins others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CG | 27 | a0001c0002t0001g0178a0001c0002t0002g0190a0001c0002t0002g0202others(24): Show | 27 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.299-556dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | CGGGGTGA others(865): Show |
1 | a0002c0001t0014g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.299-556_299-555ins others(872): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | G | 1 | a0001c0009t0050g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-555G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
C | T | 4 | a0001c0002t0002g0186a0001c0003t0002g0094a0001c0003t0028g0144others(1): Show | 4 | HG02602.hp2 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-555G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627981
|
CGGGGTGA others(95): Show |
C | 1 | a0003c0028t0043g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.299-657_299-556del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627981 | ||||||
| chr19:1627982
|
GGGGTGAG others(164): Show |
G | 1 | a0001c0002t0013g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.299-727_299-557del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627982 | ||||||
| chr19:1627982
|
GGGGTGAG others(402): Show |
G | 1 | a0002c0001t0070g0121 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.299-965_299-557del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627982 | ||||||
| chr19:1627985
|
G | A | 7 | a0001c0002t0001g0078a0001c0002t0002g0188a0001c0005t0009g0029others(4): Show | 7 | HG01175.hp1 HG02015.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-559C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627985 | ||||||
| chr19:1627985
|
G | GA | 3 | a0001c0003t0028g0144a0001c0004t0028g0101a0001c0005t0024g0002 | 3 | HG01069.hp1 NA18944.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.299-560_299-559ins others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627985 | ||||||
| chr19:1627985
|
G | GGTGGGGC others(166): Show |
1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-560_299-559ins others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627985 | ||||||
| chr19:1627985
|
G | GTGAGGCG others(28): Show |
1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.299-560_299-559ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627985 | ||||||
| chr19:1627987
|
GAGGCGGG others(164): Show |
G | 1 | a0001c0003t0028g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.299-732_299-562del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627987 | ||||||
| chr19:1627988
|
A | AGGTGGGA others(26): Show |
1 | a0001c0003t0076g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-563_299-562ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627988 | ||||||
| chr19:1627988
|
A | G | 12 | a0001c0002t0001g0173a0001c0009t0050g0168a0002c0001t0006g0067others(9): Show | 12 | HG01952.hp2 HG02132.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-562T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627988 | ||||||
| chr19:1627991
|
C | CGGGAAGG others(26): Show |
1 | a0002c0001t0015g0080 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-566_299-565ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627991 | ||||||
| chr19:1627991
|
C | T | 21 | a0001c0003t0001g0096a0001c0003t0002g0094a0001c0004t0003g0153others(18): Show | 21 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-565G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627991 | ||||||
| chr19:1627994
|
G | A | 4 | a0001c0003t0001g0152a0001c0003t0001g0227a0001c0003t0002g0001others(1): Show | 5 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-568C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627994 | ||||||
| chr19:1627997
|
G | A | 2 | a0003c0006t0002g0126a0003c0006t0012g0313 | 2 | HG00438.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.299-571C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1627997 | ||||||
| chr19:1628004
|
G | C | 1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-578C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628004 | ||||||
| chr19:1628005
|
C | T | 5 | a0001c0002t0002g0267a0001c0005t0009g0022a0001c0007t0002g0149others(2): Show | 5 | HG00597.hp2 HG02004.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-579G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628005 | ||||||
| chr19:1628009
|
G | A | 44 | a0001c0002t0001g0138a0001c0002t0041g0004a0001c0002t0078g0189others(41): Show | 44 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.299-583C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628009 | ||||||
| chr19:1628009
|
G | GCTCACAG others(229): Show |
1 | a0001c0005t0025g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.299-584_299-583ins others(236): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628009 | ||||||
| chr19:1628009
|
G | GCTCACGG others(94): Show |
1 | a0001c0019t0026g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.299-584_299-583ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628009 | ||||||
| chr19:1628009
|
GCTCACAG others(132): Show |
G | 1 | a0001c0002t0002g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.299-722_299-584del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628009 | ||||||
| chr19:1628013
|
A | ACGGGGGT others(328): Show |
1 | a0002c0001t0053g0057 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.299-588_299-587ins others(335): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGGT others(529): Show |
1 | a0002c0001t0054g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(536): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGGT others(461): Show |
1 | a0002c0001t0019g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(468): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGGT others(60): Show |
1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGGT others(92): Show |
1 | a0002c0001t0015g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(92): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(163): Show |
1 | a0002c0001t0057g0158 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.299-588_299-587ins others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(527): Show |
1 | a0003c0006t0002g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.299-588_299-587ins others(534): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(59): Show |
2 | a0001c0004t0003g0099a0001c0004t0008g0100 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.299-588_299-587ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(331): Show |
1 | a0001c0003t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(338): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(395): Show |
1 | a0002c0001t0007g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(402): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(331): Show |
1 | a0001c0005t0004g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.299-588_299-587ins others(338): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(90): Show |
1 | a0001c0002t0002g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.299-588_299-587ins others(97): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628013
|
A | ACGGGGTG others(431): Show |
1 | a0001c0002t0002g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.299-588_299-587ins others(438): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628013 | ||||||
| chr19:1628014
|
C | CGGGGTGA others(59): Show |
1 | a0002c0001t0022g0318 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.299-589_299-588ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628014 | ||||||
| chr19:1628014
|
CA | C | 25 | a0001c0002t0001g0203a0001c0002t0075g0185a0001c0002t0078g0189others(22): Show | 25 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.299-589delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628014 | ||||||
| chr19:1628014
|
CAG | C | 83 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0138others(80): Show | 83 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.299-590_299-589del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628014 | ||||||
| chr19:1628015
|
A | AGGGGGTG others(93): Show |
1 | a0003c0006t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.299-590_299-589ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628015 | ||||||
| chr19:1628015
|
A | AGGGGGTG others(27): Show |
1 | a0018c0018t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-623_299-590dup others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628015 | ||||||
| chr19:1628015
|
A | C | 1 | a0002c0001t0022g0318 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.299-589T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628015 | ||||||
| chr19:1628015
|
A | G | 13 | a0001c0002t0085g0304a0001c0003t0001g0200a0001c0003t0001g0201others(10): Show | 13 | HG01106.hp2 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-589T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628015 | ||||||
| chr19:1628016
|
G | C | 12 | a0001c0002t0002g0048a0001c0002t0002g0190a0001c0003t0002g0243others(9): Show | 12 | HG01069.hp2 HG02004.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-590C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGATGA others(59): Show |
1 | a0002c0001t0006g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.299-591_299-590ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGATGA others(428): Show |
2 | a0002c0001t0006g0055a0002c0001t0019g0056 | 2 | NA18944.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.299-591_299-590ins others(435): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGATGA others(26): Show |
6 | a0001c0003t0001g0234a0001c0003t0005g0338a0001c0003t0005g0340others(3): Show | 6 | HG00323.hp2 HG01175.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-591_299-590ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTAA others(61): Show |
1 | a0001c0002t0002g0214 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.299-591_299-590ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTGA others(26): Show |
1 | a0003c0008t0068g0268 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.299-591_299-590ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTGA others(26): Show |
1 | a0001c0004t0003g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.299-591_299-590ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTGA others(26): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-591_299-590ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTGA others(129): Show |
1 | a0001c0007t0090g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.299-591_299-590ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTGA others(196): Show |
1 | a0001c0005t0004g0027 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-591_299-590ins others(203): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTGA others(535): Show |
2 | a0001c0005t0047g0042a0019c0017t0001g0221 | 2 | HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.299-591_299-590ins others(542): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | GGGGGTGA others(401): Show |
1 | a0001c0005t0009g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.299-591_299-590ins others(408): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628016
|
G | T | 3 | a0001c0004t0003g0099a0001c0004t0008g0100a0001c0005t0030g0192 | 3 | HG00642.hp1 HG01099.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.299-590C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628016 | ||||||
| chr19:1628020
|
G | A | 17 | a0001c0002t0001g0173a0001c0002t0002g0143a0001c0002t0002g0175others(14): Show | 17 | HG00438.hp1 HG01884.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-594C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628020 | ||||||
| chr19:1628020
|
G | GTGAGGCG others(162): Show |
1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-595_299-594ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628020 | ||||||
| chr19:1628020
|
GTGAGGCG others(97): Show |
G | 1 | a0001c0003t0005g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-698_299-595del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628020 | ||||||
| chr19:1628022
|
G | A | 9 | a0001c0002t0001g0213a0001c0002t0001g0215a0001c0002t0001g0218others(6): Show | 9 | HG00609.hp1 HG01981.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-596C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628022 | ||||||
| chr19:1628023
|
A | AGGCGGGA others(27): Show |
1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-598_299-597ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628023 | ||||||
| chr19:1628023
|
A | G | 2 | a0002c0001t0006g0083a0002c0001t0022g0318 | 2 | HG00621.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.299-597T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628023 | ||||||
| chr19:1628024
|
G | GGCGGGAA others(61): Show |
1 | a0003c0006t0002g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.299-599_299-598ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628024 | ||||||
| chr19:1628026
|
C | CGGGAAGG others(264): Show |
2 | a0001c0004t0003g0091a0001c0004t0008g0103 | 2 | HG00140.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.299-601_299-600ins others(271): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628026 | ||||||
| chr19:1628026
|
C | T | 10 | a0001c0003t0076g0045a0001c0004t0008g0151a0001c0004t0066g0172others(7): Show | 10 | HG01069.hp2 HG01891.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-600G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628026 | ||||||
| chr19:1628029
|
G | A | 3 | a0001c0003t0005g0325a0001c0003t0077g0241a0001c0004t0002g0257 | 3 | HG01074.hp2 HG01975.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.299-603C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628029 | ||||||
| chr19:1628032
|
G | A | 6 | a0001c0007t0012g0323a0002c0001t0015g0080a0002c0001t0022g0318others(3): Show | 6 | HG00558.hp2 HG00621.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-606C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628032 | ||||||
| chr19:1628040
|
C | T | 4 | a0001c0007t0002g0149a0003c0006t0001g0115a0003c0006t0001g0142others(1): Show | 4 | HG00597.hp2 HG02300.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-614G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628040 | ||||||
| chr19:1628044
|
G | A | 51 | a0001c0002t0001g0138a0001c0002t0001g0212a0001c0002t0001g0265others(48): Show | 52 | HG00438.hp2 HG00544.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.299-618C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628044 | ||||||
| chr19:1628046
|
TCA | T | 3 | a0001c0004t0001g0110a0001c0004t0002g0108a0001c0004t0002g0154 | 3 | HG02109.hp1 HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.299-622_299-621del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628046 | ||||||
| chr19:1628048
|
A | ACGGGGGA others(158): Show |
1 | a0002c0001t0007g0060 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.299-623_299-622ins others(165): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGGG others(93): Show |
1 | a0001c0004t0003g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.299-623_299-622ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGGT others(126): Show |
1 | a0002c0001t0007g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.299-623_299-622ins others(133): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGGT others(92): Show |
2 | a0002c0001t0016g0052a0002c0001t0016g0269 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.299-623_299-622ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGTG others(90): Show |
1 | a0003c0006t0001g0125 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.299-623_299-622ins others(97): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGTG others(192): Show |
1 | a0002c0001t0006g0083 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.299-623_299-622ins others(199): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGTG others(24): Show |
2 | a0004c0033t0036g0350a0005c0010t0018g0169 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299-623_299-622ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGTG others(333): Show |
1 | a0001c0005t0026g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299-623_299-622ins others(340): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ACGGGGTG others(159): Show |
6 | a0002c0001t0006g0067a0002c0001t0016g0050a0002c0001t0016g0051others(3): Show | 6 | HG01952.hp2 HG02132.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-623_299-622ins others(166): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628048
|
A | ATGGGGTG others(93): Show |
1 | a0001c0003t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.299-623_299-622ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628048 | ||||||
| chr19:1628049
|
CA | C | 39 | a0001c0002t0001g0111a0001c0002t0001g0174a0001c0002t0001g0212others(36): Show | 39 | HG00408.hp1 HG00673.hp1 HG01981.hp1 others(36): Show |
intron_variant | MODIFIER | c.299-624delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628049 | ||||||
| chr19:1628049
|
CAG | C | 55 | a0001c0002t0001g0078a0001c0002t0001g0138a0001c0002t0001g0178others(52): Show | 56 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.299-625_299-624del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628049 | ||||||
| chr19:1628049
|
CAGGGGGT others(64): Show |
C | 1 | a0001c0003t0001g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.299-694_299-624del others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628049 | ||||||
| chr19:1628050
|
A | AGGGGGTG others(27): Show |
1 | a0004c0014t0079g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.299-625_299-624ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628050 | ||||||
| chr19:1628050
|
A | G | 3 | a0001c0003t0001g0200a0001c0003t0001g0201a0001c0007t0020g0289 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.299-624T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628050 | ||||||
| chr19:1628051
|
G | C | 16 | a0001c0004t0003g0104a0001c0005t0026g0037a0002c0001t0006g0067others(13): Show | 16 | HG00642.hp2 HG01070.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-625C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGATGA others(26): Show |
1 | a0003c0006t0002g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.299-626_299-625ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGATGA others(195): Show |
1 | a0001c0002t0001g0213 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.299-626_299-625ins others(202): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGATGA others(396): Show |
1 | a0001c0002t0083g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.299-626_299-625ins others(403): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGATGA others(61): Show |
1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-626_299-625ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGATGA others(125): Show |
1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-626_299-625ins others(132): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGGTGA others(162): Show |
2 | a0001c0004t0003g0099a0001c0004t0008g0100 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.299-626_299-625ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGGTGA others(26): Show |
1 | a0001c0007t0012g0323 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.299-626_299-625ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGGTGA others(58): Show |
1 | a0001c0005t0044g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.299-626_299-625ins others(65): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGGTGA others(160): Show |
1 | a0001c0007t0002g0127 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-626_299-625ins others(167): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGGTGA others(59): Show |
1 | a0001c0005t0009g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.299-626_299-625ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | GGGGGTGA others(127): Show |
1 | a0003c0006t0031g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.299-626_299-625ins others(134): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
G | T | 4 | a0001c0003t0002g0247a0001c0004t0001g0110a0001c0004t0002g0108others(1): Show | 4 | HG01943.hp2 HG02109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-625C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628051
|
GGGGGTGA others(95): Show |
G | 1 | a0001c0004t0099g0343 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.299-727_299-626del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628051 | ||||||
| chr19:1628055
|
G | A | 22 | a0001c0002t0001g0215a0001c0002t0002g0210a0001c0002t0002g0222others(19): Show | 22 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-629C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628055 | ||||||
| chr19:1628057
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.299-631C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628057 | ||||||
| chr19:1628058
|
A | AGGCGGGA others(365): Show |
1 | a0001c0004t0003g0109 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.299-633_299-632ins others(372): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628058 | ||||||
| chr19:1628058
|
A | AGGCGGGA others(60): Show |
2 | a0001c0002t0001g0132a0001c0002t0002g0133 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.299-633_299-632ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628058 | ||||||
| chr19:1628058
|
A | AGGCGGGA others(229): Show |
1 | a0004c0014t0013g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.299-633_299-632ins others(236): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628058 | ||||||
| chr19:1628058
|
A | G | 13 | a0001c0007t0001g0217a0001c0007t0074g0090a0001c0007t0096g0311others(10): Show | 13 | HG00408.hp1 HG00673.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-632T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628058 | ||||||
| chr19:1628059
|
G | C | 1 | a0001c0007t0103g0351 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.299-633C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628059 | ||||||
| chr19:1628061
|
C | CGGGAAGG others(302): Show |
1 | a0001c0002t0035g0349 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299-636_299-635ins others(309): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628061 | ||||||
| chr19:1628061
|
C | T | 21 | a0001c0003t0002g0247a0001c0004t0003g0279a0001c0004t0008g0151others(18): Show | 21 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.299-635G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628061 | ||||||
| chr19:1628062
|
G | GGGAAGGG others(128): Show |
1 | a0001c0003t0009g0007 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.299-637_299-636ins others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628062 | ||||||
| chr19:1628067
|
G | A | 1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-641C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628067 | ||||||
| chr19:1628074
|
G | C | 1 | a0003c0006t0002g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.299-648C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628074 | ||||||
| chr19:1628075
|
C | T | 2 | a0001c0002t0002g0190a0003c0006t0080g0296 | 2 | HG03486.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.299-649G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628075 | ||||||
| chr19:1628079
|
G | A | 45 | a0001c0002t0001g0173a0001c0002t0001g0209a0001c0002t0001g0215others(42): Show | 45 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.299-653C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628079 | ||||||
| chr19:1628079
|
G | GCTCACAG others(771): Show |
1 | a0002c0001t0057g0158 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.299-654_299-653ins others(778): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628079 | ||||||
| chr19:1628083
|
A | ATGGGGTG others(27): Show |
1 | a0001c0004t0021g0312 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.299-658_299-657ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628083 | ||||||
| chr19:1628083
|
AC | A | 3 | a0001c0002t0032g0161a0001c0003t0008g0098a0001c0004t0003g0220 | 3 | HG00280.hp2 HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.299-658delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628083 | ||||||
| chr19:1628083
|
ACGGGGGT others(745): Show |
A | 1 | a0001c0005t0052g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.299-1409_299-658de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628083 | ||||||
| chr19:1628084
|
C | A | 2 | a0001c0004t0021g0312a0003c0028t0043g0036 | 2 | HG02258.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.299-658G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CA | 84 | a0001c0002t0001g0138a0001c0002t0001g0178a0001c0002t0001g0181others(81): Show | 84 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.299-659_299-658ins others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(60): Show |
1 | a0001c0007t0002g0259 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(95): Show |
6 | a0001c0003t0001g0236a0001c0003t0002g0225a0001c0004t0003g0249others(3): Show | 6 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-659_299-658ins others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(442): Show |
1 | a0001c0004t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(449): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(60): Show |
1 | a0001c0003t0002g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.299-659_299-658ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(269): Show |
1 | a0001c0003t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(276): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(435): Show |
1 | a0001c0007t0091g0300 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(442): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(508): Show |
1 | a0001c0003t0002g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.299-659_299-658ins others(515): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGAT others(164): Show |
1 | a0001c0004t0086g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.299-659_299-658ins others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGGT others(744): Show |
1 | a0001c0003t0005g0325 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.299-659_299-658ins others(751): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGGT others(131): Show |
1 | a0003c0006t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CAGGGGTG others(163): Show |
1 | a0001c0003t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CG | 6 | a0001c0002t0001g0173a0001c0002t0085g0304a0001c0004t0003g0109others(3): Show | 6 | HG01106.hp1 HG01106.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-659dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CGGGGTGA others(129): Show |
4 | a0003c0006t0001g0119a0003c0006t0002g0120a0003c0006t0017g0294others(1): Show | 4 | HG00423.hp2 NA18964.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-659_299-658ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CGGGGTGA others(62): Show |
1 | a0001c0004t0008g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CGGGGTGA others(337): Show |
1 | a0001c0004t0003g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299-659_299-658ins others(344): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CGGGGTGA others(131): Show |
1 | a0001c0004t0008g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CGGGGTGA others(95): Show |
1 | a0001c0003t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.299-659_299-658ins others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | CGGGGTGA others(162): Show |
1 | a0001c0005t0004g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.299-659_299-658ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
C | T | 2 | a0001c0004t0008g0097a0005c0010t0018g0170 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.299-658G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628084
|
CG | C | 81 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0174others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.299-659delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628084 | ||||||
| chr19:1628085
|
G | A | 1 | a0001c0003t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.299-659C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | C | 3 | a0001c0003t0002g0287a0001c0003t0005g0325a0001c0007t0002g0259 | 3 | HG00423.hp1 HG01346.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.299-659C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGGTGA others(59): Show |
1 | a0001c0003t0005g0336 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGGTGA others(26): Show |
2 | a0001c0002t0001g0209a0001c0002t0001g0216 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.299-692_299-660dup others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGGTGA others(611): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(618): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGGTGA others(59): Show |
1 | a0001c0005t0001g0208 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGGTGG others(59): Show |
1 | a0001c0007t0020g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.299-660_299-659ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGGTGG others(497): Show |
1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(504): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGGTGG others(59): Show |
1 | a0002c0001t0006g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(25): Show |
1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299-660_299-659ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(193): Show |
1 | a0012c0030t0002g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(200): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(25): Show |
3 | a0001c0005t0004g0026a0001c0005t0009g0018a0016c0027t0004g0020 | 3 | HG01123.hp1 HG02293.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.299-660_299-659ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(60): Show |
1 | a0001c0004t0008g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(93): Show |
1 | a0002c0001t0007g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.299-660_299-659ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(160): Show |
1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-660_299-659ins others(167): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(93): Show |
1 | a0002c0001t0022g0318 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.299-660_299-659ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(559): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-660_299-659ins others(566): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(25): Show |
3 | a0001c0002t0065g0176a0001c0003t0076g0045a0001c0004t0003g0044 | 3 | HG02257.hp1 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.299-660_299-659ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(59): Show |
2 | a0001c0003t0001g0200a0001c0003t0001g0201 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.299-660_299-659ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(160): Show |
1 | a0001c0007t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-660_299-659ins others(167): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | GGGGTGAG others(59): Show |
1 | a0002c0001t0006g0072 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.299-660_299-659ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
G | T | 3 | a0001c0002t0032g0161a0001c0003t0008g0098a0001c0004t0003g0220 | 3 | HG00280.hp2 HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.299-659C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628085
|
GGGGGTGA others(94): Show |
G | 1 | a0001c0009t0049g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.299-760_299-660del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628085 | ||||||
| chr19:1628089
|
G | A | 18 | a0001c0002t0001g0178a0001c0002t0005g0319a0001c0002t0005g0330others(15): Show | 18 | HG01071.hp1 HG01243.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-663C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628089 | ||||||
| chr19:1628091
|
G | A | 1 | a0001c0002t0002g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.299-665C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628091 | ||||||
| chr19:1628092
|
A | G | 28 | a0001c0002t0001g0180a0001c0002t0085g0304a0001c0003t0002g0243others(25): Show | 28 | HG00609.hp2 HG00673.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.299-666T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628092 | ||||||
| chr19:1628093
|
G | T | 2 | a0001c0002t0002g0190a0003c0006t0002g0077 | 2 | HG00558.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.299-667C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628093 | ||||||
| chr19:1628095
|
C | T | 11 | a0001c0004t0003g0153a0001c0004t0011g0136a0001c0004t0011g0137others(8): Show | 11 | HG00408.hp1 HG01074.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-669G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628095 | ||||||
| chr19:1628098
|
G | A | 8 | a0001c0003t0001g0236a0001c0003t0002g0225a0001c0003t0002g0229others(5): Show | 8 | HG00099.hp2 HG01261.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-672C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628098 | ||||||
| chr19:1628101
|
G | A | 4 | a0001c0004t0003g0091a0002c0001t0006g0072a0003c0006t0001g0092others(1): Show | 4 | HG00140.hp2 NA19056.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-675C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628101 | ||||||
| chr19:1628109
|
C | T | 2 | a0001c0002t0004g0012a0001c0002t0035g0349 | 2 | HG01346.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.299-683G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628109 | ||||||
| chr19:1628113
|
G | A | 54 | a0001c0002t0001g0138a0001c0002t0001g0173a0001c0002t0002g0188others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.299-687C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628113 | ||||||
| chr19:1628113
|
G | GCTCACAG others(199): Show |
3 | a0001c0005t0004g0023a0001c0005t0004g0028a0001c0005t0045g0040 | 3 | HG01167.hp1 HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.299-688_299-687ins others(206): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628113 | ||||||
| chr19:1628113
|
GCTCACAG others(28): Show |
G | 1 | a0001c0013t0037g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.299-722_299-688del others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628113 | ||||||
| chr19:1628117
|
A | ACGGGGTG others(59): Show |
5 | a0001c0025t0010g0266a0002c0001t0001g0122a0003c0006t0010g0141others(2): Show | 5 | NA18955.hp1 NA18963.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-692_299-691ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628117 | ||||||
| chr19:1628117
|
A | ACGGGGTG others(262): Show |
1 | a0001c0004t0002g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.299-692_299-691ins others(269): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628117 | ||||||
| chr19:1628118
|
C | CGGGGGTG others(93): Show |
1 | a0001c0003t0002g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.299-693_299-692ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
C | CGGGGGTG others(428): Show |
1 | a0002c0001t0034g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.299-693_299-692ins others(435): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
C | CGGGGGTG others(163): Show |
1 | a0001c0004t0003g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-693_299-692ins others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
C | CGGGGTGA others(226): Show |
3 | a0002c0001t0006g0067a0002c0001t0016g0051a0002c0001t0056g0206 | 3 | NA18945.hp2 NA18989.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.299-693_299-692ins others(233): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
C | CGGGGTGA others(25): Show |
1 | a0001c0002t0075g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-693_299-692ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
C | CGGGGTGA others(93): Show |
1 | a0001c0005t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.299-693_299-692ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
CA | C | 46 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0001g0218others(43): Show | 46 | HG00408.hp1 HG00735.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.299-693delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
CAG | C | 63 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0180others(60): Show | 64 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.299-694_299-693del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628118
|
CAGGGGAT others(96): Show |
C | 1 | a0001c0003t0077g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.299-795_299-693del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628118 | ||||||
| chr19:1628119
|
A | AGGGGGTG others(129): Show |
1 | a0001c0003t0033g0324 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.299-694_299-693ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628119 | ||||||
| chr19:1628119
|
A | C | 8 | a0001c0002t0075g0185a0001c0003t0002g0253a0001c0004t0003g0285others(5): Show | 8 | HG02647.hp2 HG03041.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-693T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628119 | ||||||
| chr19:1628119
|
A | G | 5 | a0001c0002t0002g0188a0001c0005t0001g0183a0001c0007t0020g0289others(2): Show | 5 | HG01891.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-693T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628119 | ||||||
| chr19:1628120
|
G | C | 6 | a0001c0004t0002g0108a0001c0025t0010g0266a0002c0001t0001g0122others(3): Show | 6 | NA18955.hp1 NA18963.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-694C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628120
|
G | GGGGGTGA others(92): Show |
1 | a0014c0020t0034g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.299-695_299-694ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628120
|
G | GGGGGTGA others(61): Show |
1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.299-695_299-694ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628120
|
G | GGGGGTGA others(163): Show |
1 | a0001c0002t0085g0304 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.299-695_299-694ins others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628120
|
G | GGGGGTGA others(94): Show |
1 | a0020c0034t0010g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.299-695_299-694ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628120
|
G | GGGGGTGA others(59): Show |
1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-695_299-694ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628120
|
GGGGATGA others(26): Show |
G | 2 | a0002c0001t0100g0342a0003c0008t0082g0299 | 2 | HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.299-727_299-695del others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628120
|
GGGGATGA others(161): Show |
G | 1 | a0001c0005t0004g0019 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.299-862_299-695del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628120 | ||||||
| chr19:1628123
|
GA | G | 8 | a0001c0002t0032g0161a0001c0003t0001g0096a0001c0003t0001g0226others(5): Show | 8 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-698delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628123 | ||||||
| chr19:1628124
|
A | ATGAGGCG others(26): Show |
1 | a0007c0016t0002g0260 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.299-731_299-699dup others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628124 | ||||||
| chr19:1628124
|
A | ATGAGGCG others(296): Show |
1 | a0003c0006t0035g0345 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.299-699_299-698ins others(303): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628124 | ||||||
| chr19:1628124
|
A | G | 218 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0001g0173others(215): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.299-698T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628124 | ||||||
| chr19:1628124
|
ATGAGGCG others(59): Show |
A | 1 | a0005c0010t0018g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-764_299-699del others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628124 | ||||||
| chr19:1628124
|
ATGAGGCG others(810): Show |
A | 2 | a0001c0003t0002g0245a0001c0003t0032g0237 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.299-1515_299-699de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628124 | ||||||
| chr19:1628127
|
A | G | 16 | a0001c0002t0001g0132a0001c0002t0001g0218a0001c0002t0002g0133others(13): Show | 16 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-701T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628127 | ||||||
| chr19:1628128
|
G | C | 2 | a0004c0033t0036g0350a0005c0010t0018g0169 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299-702C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628128 | ||||||
| chr19:1628128
|
G | T | 1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299-702C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628128 | ||||||
| chr19:1628130
|
C | CGGGAAGG others(27): Show |
1 | a0001c0007t0003g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-705_299-704ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628130 | ||||||
| chr19:1628130
|
C | T | 17 | a0001c0002t0001g0173a0001c0004t0066g0172a0001c0007t0002g0049others(14): Show | 17 | HG00609.hp2 HG01943.hp1 HG02273.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-704G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628130 | ||||||
| chr19:1628136
|
G | A | 7 | a0001c0003t0001g0096a0001c0003t0008g0098a0001c0003t0059g0187others(4): Show | 7 | HG00280.hp2 HG00558.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-710C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628136 | ||||||
| chr19:1628136
|
G | GGGGACAG others(467): Show |
1 | a0003c0006t0001g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.299-711_299-710ins others(474): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628136 | ||||||
| chr19:1628148
|
A | G | 140 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(137): Show | 140 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.299-722T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628148 | ||||||
| chr19:1628150
|
T | TCATGGGG others(164): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-725_299-724ins others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628150 | ||||||
| chr19:1628153
|
C | CAG | 40 | a0001c0002t0001g0138a0001c0002t0002g0048a0001c0002t0004g0012others(37): Show | 40 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.299-728_299-727ins others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CAGGGGGT others(132): Show |
1 | a0001c0005t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.299-728_299-727ins others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CAGGGGGT others(202): Show |
1 | a0016c0027t0004g0020 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.299-728_299-727ins others(209): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CAGGGGGT others(29): Show |
1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-728_299-727ins others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CAGGGGGT others(98): Show |
7 | a0001c0003t0001g0236a0001c0003t0002g0225a0001c0004t0003g0249others(4): Show | 7 | HG00099.hp2 HG00735.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-728_299-727ins others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CAGGGGGT others(131): Show |
1 | a0001c0004t0081g0302 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.299-728_299-727ins others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CG | 40 | a0001c0002t0001g0173a0001c0002t0001g0215a0001c0002t0002g0188others(37): Show | 40 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.299-728dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGGTG others(28): Show |
1 | a0001c0007t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.299-728_299-727ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGGTG others(233): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-728_299-727ins others(240): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGGTG others(29): Show |
1 | a0001c0004t0002g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-728_299-727ins others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGGTG others(61): Show |
4 | a0002c0001t0006g0055a0002c0001t0019g0056a0002c0001t0019g0284others(1): Show | 4 | HG02056.hp1 NA18944.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-728_299-727ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGGTG others(128): Show |
1 | a0002c0001t0007g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.299-728_299-727ins others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGGTG others(162): Show |
1 | a0002c0001t0054g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.299-728_299-727ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGTGA others(97): Show |
1 | a0001c0005t0024g0003 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.299-728_299-727ins others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGTGA others(28): Show |
1 | a0001c0003t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-728_299-727ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGTGA others(61): Show |
3 | a0001c0004t0003g0153a0001c0004t0011g0136a0001c0004t0011g0137 | 3 | HG01074.hp1 HG01257.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.299-728_299-727ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGTGA others(28): Show |
2 | a0001c0004t0008g0097a0002c0001t0029g0159 | 2 | HG00639.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.299-728_299-727ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGTGA others(27): Show |
5 | a0002c0001t0007g0085a0002c0001t0019g0084a0002c0001t0069g0082others(2): Show | 5 | HG00673.hp1 NA19000.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-728_299-727ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | CGGGGTGA others(263): Show |
1 | a0002c0001t0015g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-728_299-727ins others(270): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | G | 1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-727G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
C | T | 4 | a0001c0002t0058g0283a0001c0004t0003g0280a0001c0004t0011g0134others(1): Show | 4 | HG00741.hp2 HG02015.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-727G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628153
|
CGGGGTGA others(336): Show |
C | 1 | a0006c0012t0020g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.299-1070_299-728de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628153 | ||||||
| chr19:1628157
|
G | A | 5 | a0001c0002t0001g0138a0001c0004t0099g0343a0001c0007t0001g0232others(2): Show | 5 | HG00597.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-731C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628157 | ||||||
| chr19:1628157
|
G | GA | 5 | a0001c0004t0003g0099a0001c0004t0008g0100a0001c0004t0011g0102others(2): Show | 5 | HG00642.hp1 HG01099.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-732_299-731ins others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628157 | ||||||
| chr19:1628157
|
G | GGTGGGGC others(99): Show |
1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-732_299-731ins others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628157 | ||||||
| chr19:1628157
|
G | GGTGGGGC others(333): Show |
1 | a0001c0003t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299-732_299-731ins others(340): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628157 | ||||||
| chr19:1628157
|
G | GGTGGGGC others(401): Show |
1 | a0009c0021t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299-732_299-731ins others(408): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628157 | ||||||
| chr19:1628160
|
A | G | 6 | a0001c0002t0002g0186a0001c0003t0002g0243a0001c0003t0002g0253others(3): Show | 6 | HG03225.hp2 HG03540.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-734T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628160 | ||||||
| chr19:1628161
|
G | A | 1 | a0001c0003t0028g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.299-735C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628161 | ||||||
| chr19:1628163
|
C | T | 24 | a0001c0002t0005g0319a0001c0003t0002g0247a0001c0004t0001g0110others(21): Show | 24 | HG00621.hp1 HG00642.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.299-737G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628163 | ||||||
| chr19:1628164
|
G | A | 1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-738C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628164 | ||||||
| chr19:1628166
|
G | A | 2 | a0001c0003t0001g0165a0018c0018t0001g0164 | 2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.299-740C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628166 | ||||||
| chr19:1628169
|
G | A | 4 | a0003c0006t0002g0126a0003c0006t0002g0147a0003c0006t0012g0313others(1): Show | 4 | HG00438.hp2 HG00544.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-743C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628169 | ||||||
| chr19:1628176
|
G | C | 2 | a0001c0004t0003g0091a0001c0004t0008g0103 | 2 | HG00140.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.299-750C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628176 | ||||||
| chr19:1628177
|
C | CAGAGCTC others(27): Show |
6 | a0003c0006t0001g0115a0003c0006t0001g0119a0003c0006t0002g0120others(3): Show | 6 | HG00423.hp2 NA18950.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-752_299-751ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628177 | ||||||
| chr19:1628177
|
C | T | 2 | a0001c0002t0001g0173a0001c0007t0002g0149 | 2 | HG02300.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.299-751G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628177 | ||||||
| chr19:1628181
|
G | A | 71 | a0001c0002t0002g0191a0001c0002t0004g0012a0001c0002t0013g0182others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.299-755C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628181
|
G | GCTCACAG others(98): Show |
1 | a0001c0003t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.299-756_299-755ins others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628181
|
G | GCTCACAG others(167): Show |
1 | a0001c0005t0009g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.299-756_299-755ins others(174): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628181
|
G | GCTCACAG others(168): Show |
1 | a0001c0005t0044g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.299-756_299-755ins others(175): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628181
|
G | GCTCACAG others(197): Show |
1 | a0001c0002t0041g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.299-756_299-755ins others(204): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628181
|
G | GCTCACGG others(61): Show |
1 | a0001c0019t0026g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.299-756_299-755ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628181
|
G | GCTCACGG others(27): Show |
8 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0216others(5): Show | 8 | HG01256.hp1 HG01433.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-756_299-755ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628181
|
G | GCTCACGG others(61): Show |
1 | a0001c0002t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.299-756_299-755ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628181 | ||||||
| chr19:1628186
|
C | CAG | 51 | a0001c0002t0001g0173a0001c0002t0001g0181a0001c0002t0002g0048others(48): Show | 51 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.299-761_299-760ins others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGAT others(28): Show |
1 | a0001c0002t0078g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGAT others(30): Show |
1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGAT others(63): Show |
1 | a0001c0005t0025g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(30): Show |
1 | a0001c0004t0003g0246 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(166): Show |
1 | a0001c0004t0011g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(30): Show |
1 | a0003c0008t0068g0268 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(265): Show |
3 | a0001c0004t0003g0105a0001c0004t0003g0106a0001c0004t0011g0145 | 3 | HG00735.hp2 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.299-761_299-760ins others(272): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(30): Show |
1 | a0001c0002t0002g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(65): Show |
1 | a0001c0003t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(63): Show |
1 | a0001c0003t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(64): Show |
1 | a0001c0004t0003g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CAGGGGGT others(689): Show |
1 | a0001c0004t0021g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(696): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CG | 40 | a0001c0002t0001g0111a0001c0002t0002g0143a0001c0002t0002g0191others(37): Show | 40 | HG00597.hp2 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.299-761dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CGGGGGTG others(305): Show |
1 | a0001c0005t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(312): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CGGGGGTG others(98): Show |
1 | a0001c0004t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CGGGGGTG others(197): Show |
1 | a0001c0005t0009g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(204): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CGGGGGTG others(97): Show |
1 | a0001c0003t0005g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-761_299-760ins others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CGGGGGTG others(61): Show |
1 | a0002c0001t0006g0072 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | CGGGGTGA others(304): Show |
1 | a0001c0003t0002g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.299-761_299-760ins others(311): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | G | 2 | a0001c0007t0074g0090a0001c0007t0096g0311 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.299-760G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
C | T | 2 | a0001c0002t0002g0186a0003c0006t0001g0128 | 2 | HG02683.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-760G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628186
|
CGGGGTGA others(27): Show |
C | 1 | a0001c0004t0011g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.299-794_299-761del others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628186 | ||||||
| chr19:1628190
|
G | A | 6 | a0001c0004t0003g0246a0001c0004t0003g0279a0001c0005t0025g0038others(3): Show | 6 | HG00558.hp2 HG01243.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-764C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628190 | ||||||
| chr19:1628190
|
G | GA | 3 | a0001c0005t0004g0010a0001c0005t0026g0037a0003c0006t0001g0128 | 3 | HG01934.hp2 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.299-765_299-764ins others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628190 | ||||||
| chr19:1628190
|
G | GTGAGGCG others(28): Show |
1 | a0001c0007t0002g0259 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.299-765_299-764ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628190 | ||||||
| chr19:1628190
|
G | GTGAGGTG others(62): Show |
2 | a0001c0003t0001g0200a0001c0003t0001g0201 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.299-765_299-764ins others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628190 | ||||||
| chr19:1628193
|
A | G | 9 | a0001c0002t0002g0191a0001c0002t0032g0161a0001c0004t0003g0280others(6): Show | 9 | HG02257.hp2 HG02486.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-767T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628193 | ||||||
| chr19:1628194
|
G | T | 2 | a0001c0004t0008g0103a0003c0008t0068g0268 | 2 | HG00323.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.299-768C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628194 | ||||||
| chr19:1628196
|
C | A | 1 | a0003c0006t0001g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.299-770G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628196 | ||||||
| chr19:1628196
|
C | T | 20 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0013g0197others(17): Show | 20 | HG00597.hp1 HG01106.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-770G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628196 | ||||||
| chr19:1628199
|
G | A | 4 | a0001c0003t0001g0226a0001c0003t0001g0230a0001c0003t0002g0275others(1): Show | 4 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-773C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628199 | ||||||
| chr19:1628202
|
G | A | 1 | a0003c0006t0002g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.299-776C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628202 | ||||||
| chr19:1628209
|
G | C | 1 | a0001c0004t0003g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299-783C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628209 | ||||||
| chr19:1628214
|
G | A | 24 | a0001c0002t0001g0173a0001c0002t0002g0190a0001c0002t0013g0182others(21): Show | 24 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-788C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628214 | ||||||
| chr19:1628214
|
G | GCTCACAG others(231): Show |
1 | a0001c0002t0004g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-789_299-788ins others(238): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628214 | ||||||
| chr19:1628218
|
A | ACGGGGGT others(25): Show |
1 | a0001c0005t0026g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299-793_299-792ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGGT others(628): Show |
1 | a0002c0001t0022g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-793_299-792ins others(635): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGGT others(92): Show |
1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-793_299-792ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGGT others(196): Show |
1 | a0002c0001t0015g0080 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-793_299-792ins others(203): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGGT others(92): Show |
8 | a0002c0001t0006g0083a0002c0001t0006g0089a0002c0001t0007g0060others(5): Show | 8 | HG01952.hp2 HG02083.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-793_299-792ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(59): Show |
2 | a0001c0002t0002g0191a0018c0018t0001g0164 | 2 | HG01168.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.299-793_299-792ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(93): Show |
1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-793_299-792ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(195): Show |
1 | a0001c0002t0002g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.299-793_299-792ins others(202): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(158): Show |
1 | a0001c0002t0035g0349 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299-793_299-792ins others(165): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(156): Show |
1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.299-793_299-792ins others(163): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(125): Show |
1 | a0001c0004t0003g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-793_299-792ins others(132): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(24): Show |
1 | a0001c0003t0076g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-793_299-792ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(92): Show |
1 | a0001c0002t0005g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.299-793_299-792ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628218
|
A | ACGGGGTG others(92): Show |
2 | a0004c0033t0036g0350a0005c0010t0018g0169 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299-793_299-792ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628218 | ||||||
| chr19:1628219
|
C | CGGGGGTG others(268): Show |
1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-794_299-793ins others(275): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628219 | ||||||
| chr19:1628219
|
C | CGGGGTGA others(126): Show |
1 | a0002c0001t0007g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.299-794_299-793ins others(133): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628219 | ||||||
| chr19:1628219
|
C | CGGGGTGA others(60): Show |
1 | a0002c0001t0006g0075 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.299-794_299-793ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628219 | ||||||
| chr19:1628219
|
CA | C | 26 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0093g0341others(23): Show | 26 | HG00621.hp1 HG00642.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.299-794delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628219 | ||||||
| chr19:1628219
|
CAG | C | 32 | a0001c0002t0002g0143a0001c0002t0002g0188a0001c0002t0005g0328others(29): Show | 32 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.299-795_299-794del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628219 | ||||||
| chr19:1628220
|
A | AGGGGATG others(27): Show |
1 | a0001c0004t0003g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-795_299-794ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628220 | ||||||
| chr19:1628220
|
A | AGGGGGTG others(129): Show |
2 | a0001c0003t0005g0332a0001c0003t0012g0333 | 2 | HG00140.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.299-795_299-794ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628220 | ||||||
| chr19:1628220
|
A | C | 3 | a0002c0001t0006g0075a0002c0001t0007g0064a0005c0010t0018g0171 | 3 | HG02559.hp2 NA18963.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.299-794T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628220 | ||||||
| chr19:1628220
|
A | G | 4 | a0001c0002t0001g0173a0001c0009t0049g0167a0003c0011t0030g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-794T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628220 | ||||||
| chr19:1628220
|
A | T | 2 | a0001c0007t0103g0351a0002c0001t0100g0342 | 2 | HG02258.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.299-794T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628220 | ||||||
| chr19:1628221
|
G | C | 20 | a0001c0002t0001g0111a0001c0002t0002g0186a0001c0002t0002g0191others(17): Show | 20 | HG01168.hp2 HG01358.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-795C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628221 | ||||||
| chr19:1628221
|
G | GGGGATGA others(26): Show |
3 | a0001c0002t0001g0213a0001c0002t0001g0215a0001c0003t0001g0165 | 3 | HG00099.hp1 HG02273.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.299-796_299-795ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628221 | ||||||
| chr19:1628221
|
G | GGGGATGA others(196): Show |
1 | a0020c0034t0010g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.299-796_299-795ins others(203): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628221 | ||||||
| chr19:1628221
|
G | GGGGGTGA others(26): Show |
1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.299-796_299-795ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628221 | ||||||
| chr19:1628221
|
G | GGGGGTGA others(26): Show |
1 | a0001c0004t0008g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.299-796_299-795ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628221 | ||||||
| chr19:1628221
|
G | GGGGGTGA others(26): Show |
1 | a0001c0007t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.299-828_299-796dup others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628221 | ||||||
| chr19:1628221
|
G | T | 4 | a0001c0004t0003g0280a0001c0004t0021g0312a0004c0033t0036g0350others(1): Show | 4 | HG01109.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-795C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628221 | ||||||
| chr19:1628225
|
G | A | 34 | a0001c0002t0001g0181a0001c0002t0001g0218a0001c0002t0002g0175others(31): Show | 34 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.299-799C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628225 | ||||||
| chr19:1628225
|
G | GTGAGGCG others(27): Show |
1 | a0001c0005t0025g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.299-800_299-799ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628225 | ||||||
| chr19:1628225
|
G | GTGAGGCG others(164): Show |
2 | a0001c0002t0046g0039a0001c0005t0040g0006 | 2 | HG01109.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.299-800_299-799ins others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628225 | ||||||
| chr19:1628228
|
A | AGGCGGGA others(330): Show |
1 | a0001c0004t0011g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-803_299-802ins others(337): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628228 | ||||||
| chr19:1628228
|
A | AGGCGGGA others(128): Show |
1 | a0002c0001t0006g0063 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.299-803_299-802ins others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628228 | ||||||
| chr19:1628228
|
A | G | 18 | a0001c0003t0028g0144a0001c0003t0076g0045a0001c0004t0001g0110others(15): Show | 18 | HG00621.hp1 HG00642.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-802T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628228 | ||||||
| chr19:1628229
|
G | T | 1 | a0001c0004t0003g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299-803C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628229 | ||||||
| chr19:1628231
|
C | CGGGAAGG others(127): Show |
2 | a0002c0001t0073g0079a0002c0001t0092g0295 | 2 | NA18947.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.299-806_299-805ins others(134): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628231 | ||||||
| chr19:1628231
|
C | CGGGAAGG others(60): Show |
3 | a0001c0007t0001g0217a0002c0001t0006g0076a0002c0001t0034g0309 | 3 | HG00408.hp1 HG02132.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.299-806_299-805ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628231 | ||||||
| chr19:1628231
|
C | T | 18 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0002g0188others(15): Show | 18 | HG00280.hp2 HG00741.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-805G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628231 | ||||||
| chr19:1628232
|
G | A | 1 | a0001c0003t0028g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.299-806C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628232 | ||||||
| chr19:1628234
|
G | A | 5 | a0001c0003t0005g0326a0001c0004t0003g0286a0001c0004t0008g0251others(2): Show | 5 | HG01978.hp1 HG02055.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-808C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628234 | ||||||
| chr19:1628237
|
G | A | 6 | a0001c0004t0003g0105a0001c0004t0003g0106a0001c0004t0008g0103others(3): Show | 6 | HG00735.hp2 HG01123.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-811C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628237 | ||||||
| chr19:1628245
|
C | T | 2 | a0003c0008t0001g0118a0020c0034t0010g0146 | 2 | HG02735.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.299-819G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628245 | ||||||
| chr19:1628249
|
G | A | 37 | a0001c0002t0001g0138a0001c0002t0001g0173a0001c0002t0078g0189others(34): Show | 37 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.299-823C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628249 | ||||||
| chr19:1628249
|
G | ACTCACGG others(162): Show |
1 | a0001c0003t0005g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-823_299-822ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628249 | ||||||
| chr19:1628250
|
C | T | 1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-824G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628250 | ||||||
| chr19:1628254
|
C | CA | 74 | a0001c0002t0001g0180a0001c0002t0002g0186a0001c0002t0002g0191others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.299-829_299-828ins others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CAGGGGAT others(29): Show |
1 | a0001c0004t0003g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-829_299-828ins others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CAGGGGAT others(129): Show |
1 | a0003c0006t0035g0345 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.299-829_299-828ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CAGGGGAT others(130): Show |
1 | a0001c0003t0002g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.299-829_299-828ins others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CAGGGGGT others(98): Show |
1 | a0001c0005t0004g0017 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.299-829_299-828ins others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CAGGGGGT others(96): Show |
1 | a0012c0030t0002g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.299-829_299-828ins others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CAGGGGTG others(95): Show |
2 | a0001c0002t0001g0132a0001c0002t0002g0133 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.299-829_299-828ins others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGATG others(28): Show |
1 | a0001c0005t0004g0005 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.299-829_299-828ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGATG others(402): Show |
1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-829_299-828ins others(409): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGGTG others(28): Show |
1 | a0001c0003t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.299-829_299-828ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGGTG others(467): Show |
1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-829_299-828ins others(474): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGGTG others(63): Show |
1 | a0001c0005t0039g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.299-829_299-828ins others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGGTG others(28): Show |
1 | a0001c0004t0086g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.299-829_299-828ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGTGA others(27): Show |
1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.299-829_299-828ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | CGGGGTGA others(230): Show |
1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299-829_299-828ins others(237): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
C | T | 2 | a0002c0001t0015g0155a0005c0010t0018g0171 | 2 | HG01978.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.299-828G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628254
|
CG | C | 65 | a0001c0002t0001g0138a0001c0002t0001g0173a0001c0002t0001g0181others(62): Show | 65 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.299-829delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628254 | ||||||
| chr19:1628255
|
G | A | 5 | a0001c0004t0003g0099a0001c0004t0008g0100a0001c0004t0021g0312others(2): Show | 5 | HG00408.hp2 HG00642.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-829C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | C | 2 | a0001c0002t0001g0132a0001c0002t0002g0133 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.299-829C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGGGTG others(130): Show |
1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-830_299-829ins others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGGTGA others(26): Show |
1 | a0001c0002t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299-862_299-830dup others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGGTGA others(61): Show |
1 | a0001c0002t0065g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.299-830_299-829ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGGTGA others(193): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-830_299-829ins others(200): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGGTGG others(26): Show |
2 | a0002c0001t0016g0052a0002c0001t0016g0269 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.299-830_299-829ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(25): Show |
1 | a0003c0008t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-830_299-829ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(25): Show |
1 | a0001c0002t0002g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.299-830_299-829ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(195): Show |
1 | a0006c0012t0020g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.299-830_299-829ins others(202): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(126): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-830_299-829ins others(133): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(60): Show |
1 | a0001c0005t0004g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.299-830_299-829ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(129): Show |
1 | a0001c0003t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-830_299-829ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(93): Show |
1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-830_299-829ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(59): Show |
1 | a0003c0006t0001g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.299-830_299-829ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628255
|
G | GGGGTGAG others(162): Show |
1 | a0001c0002t0032g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-830_299-829ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628255 | ||||||
| chr19:1628258
|
GGTGAGGC others(62): Show |
G | 1 | a0001c0004t0028g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.299-901_299-833del others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628258 | ||||||
| chr19:1628259
|
G | A | 31 | a0001c0002t0041g0004a0001c0003t0001g0165a0001c0003t0002g0095others(28): Show | 31 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.299-833C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628259 | ||||||
| chr19:1628259
|
G | GTGAGGCG others(62): Show |
1 | a0001c0003t0055g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.299-834_299-833ins others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628259 | ||||||
| chr19:1628259
|
G | GTGAGGCG others(28): Show |
1 | a0001c0002t0002g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-834_299-833ins others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628259 | ||||||
| chr19:1628261
|
G | A | 1 | a0001c0002t0002g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.299-835C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628261 | ||||||
| chr19:1628261
|
G | GAGGCGGG others(59): Show |
2 | a0001c0002t0002g0222a0001c0005t0002g0224 | 2 | HG00609.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.299-836_299-835ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628261 | ||||||
| chr19:1628262
|
A | G | 27 | a0001c0002t0002g0175a0001c0002t0005g0330a0001c0003t0002g0242others(24): Show | 27 | HG00621.hp1 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.299-836T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628262 | ||||||
| chr19:1628265
|
C | T | 7 | a0001c0002t0001g0173a0001c0003t0001g0096a0001c0003t0002g0243others(4): Show | 7 | HG02486.hp1 HG02683.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-839G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628265 | ||||||
| chr19:1628266
|
G | A | 1 | a0001c0003t0077g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.299-840C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628266 | ||||||
| chr19:1628268
|
G | A | 1 | a0002c0001t0015g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-842C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628268 | ||||||
| chr19:1628271
|
G | A | 11 | a0001c0003t0001g0228a0001c0003t0002g0001a0001c0003t0002g0095others(8): Show | 12 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-845C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628271 | ||||||
| chr19:1628279
|
C | T | 3 | a0001c0007t0002g0149a0003c0006t0002g0077a0003c0008t0001g0118 | 3 | HG00558.hp2 HG02300.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.299-853G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628279 | ||||||
| chr19:1628283
|
G | A | 99 | a0001c0002t0001g0213a0001c0002t0001g0215a0001c0002t0002g0191others(96): Show | 99 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.299-857C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628283 | ||||||
| chr19:1628287
|
ACGGGGTG others(94): Show |
A | 1 | a0002c0001t0100g0342 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.299-962_299-862del | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628287 | ||||||
| chr19:1628287
|
ACGGGGTG others(574): Show |
A | 1 | a0003c0006t0001g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.299-1442_299-862de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628287 | ||||||
| chr19:1628288
|
C | CAG | 37 | a0001c0002t0058g0283a0001c0002t0078g0189a0001c0003t0001g0165others(34): Show | 38 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.299-863_299-862ins others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGAT others(29): Show |
4 | a0001c0025t0010g0266a0003c0006t0010g0141a0003c0006t0017g0297others(1): Show | 4 | NA18963.hp1 NA18989.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-863_299-862ins others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGAT others(781): Show |
1 | a0002c0001t0001g0122 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.299-863_299-862ins others(788): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGAT others(374): Show |
1 | a0001c0003t0005g0336 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.299-863_299-862ins others(381): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGGT others(30): Show |
1 | a0001c0002t0075g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-863_299-862ins others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGGT others(64): Show |
1 | a0001c0003t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.299-863_299-862ins others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGGT others(166): Show |
1 | a0001c0004t0008g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-863_299-862ins others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGGT others(133): Show |
1 | a0001c0004t0003g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.299-863_299-862ins others(140): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGGT others(98): Show |
1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-863_299-862ins others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGGT others(30): Show |
1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.299-863_299-862ins others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CAGGGGTG others(337): Show |
1 | a0001c0007t0002g0127 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-863_299-862ins others(344): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CG | 32 | a0001c0002t0001g0173a0001c0004t0001g0166a0001c0004t0003g0153others(29): Show | 32 | HG00423.hp2 HG00621.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.299-863dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CGGGGGTG others(132): Show |
1 | a0001c0005t0009g0013 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.299-863_299-862ins others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CGGGGTGA others(163): Show |
1 | a0001c0005t0004g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.299-863_299-862ins others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628288
|
C | CGGGGTGA others(131): Show |
1 | a0003c0006t0001g0125 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.299-863_299-862ins others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628288 | ||||||
| chr19:1628289
|
G | GGGGGTGA others(779): Show |
1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-864_299-863ins others(786): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628289 | ||||||
| chr19:1628292
|
G | A | 8 | a0001c0002t0058g0283a0001c0002t0078g0189a0001c0004t0003g0044others(5): Show | 8 | HG00544.hp1 HG02148.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-866C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628292 | ||||||
| chr19:1628292
|
G | GGTGAGGC others(230): Show |
1 | a0001c0005t0004g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.299-867_299-866ins others(237): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628292 | ||||||
| chr19:1628292
|
G | GTGAGGCG others(234): Show |
1 | a0001c0002t0005g0330 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.299-867_299-866ins others(241): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628292 | ||||||
| chr19:1628295
|
A | AGGCGGGA others(195): Show |
1 | a0001c0004t0021g0312 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.299-870_299-869ins others(202): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628295 | ||||||
| chr19:1628295
|
A | AGGCGGGA others(59): Show |
1 | a0001c0002t0002g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-870_299-869ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628295 | ||||||
| chr19:1628295
|
A | AGGCGGGA others(26): Show |
1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.299-870_299-869ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628295 | ||||||
| chr19:1628295
|
A | G | 12 | a0001c0002t0001g0180a0001c0002t0002g0186a0001c0002t0005g0319others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-869T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628295 | ||||||
| chr19:1628296
|
G | GGTGGGAA others(63): Show |
1 | a0001c0004t0008g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.299-871_299-870ins others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628296 | ||||||
| chr19:1628296
|
G | T | 1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-870C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628296 | ||||||
| chr19:1628298
|
C | T | 23 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0032g0161others(20): Show | 23 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.299-872G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628298 | ||||||
| chr19:1628299
|
G | A | 1 | a0001c0004t0003g0246 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.299-873C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628299 | ||||||
| chr19:1628301
|
G | A | 1 | a0001c0013t0037g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.299-875C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628301 | ||||||
| chr19:1628304
|
G | A | 4 | a0001c0003t0001g0152a0001c0004t0003g0109a0003c0006t0002g0147others(1): Show | 4 | HG01106.hp1 HG01257.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-878C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628304 | ||||||
| chr19:1628311
|
G | C | 4 | a0001c0004t0003g0099a0001c0004t0102g0344a0003c0006t0002g0077others(1): Show | 4 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-885C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628311 | ||||||
| chr19:1628312
|
C | T | 4 | a0001c0007t0002g0127a0001c0007t0002g0149a0002c0001t0001g0122others(1): Show | 4 | HG02071.hp1 HG02300.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-886G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628312 | ||||||
| chr19:1628316
|
G | A | 20 | a0001c0002t0002g0210a0001c0004t0003g0109a0001c0005t0004g0026others(17): Show | 20 | HG00621.hp1 HG01106.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-890C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628316 | ||||||
| chr19:1628316
|
GCTCACAG others(63): Show |
G | 1 | a0001c0004t0003g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.299-960_299-891del others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628316 | ||||||
| chr19:1628316
|
GCTCACAG others(304): Show |
G | 1 | a0001c0002t0002g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.299-1201_299-891de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628316 | ||||||
| chr19:1628320
|
A | ACGGGGGT others(25): Show |
3 | a0001c0007t0074g0090a0001c0007t0096g0311a0002c0001t0007g0071 | 3 | HG03490.hp1 HG03492.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.299-895_299-894ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628320
|
A | ACGGGGGT others(227): Show |
1 | a0002c0001t0029g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.299-895_299-894ins others(234): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628320
|
A | ACGGGGTA others(24): Show |
2 | a0001c0002t0005g0322a0001c0029t0002g0162 | 2 | HG02083.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.299-895_299-894ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628320
|
A | ACGGGGTG others(195): Show |
1 | a0001c0002t0002g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-895_299-894ins others(202): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628320
|
A | ACGGGGTG others(59): Show |
1 | a0001c0003t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299-895_299-894ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628320
|
A | ACGGGGTG others(362): Show |
1 | a0001c0002t0085g0304 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.299-895_299-894ins others(369): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628320
|
A | ACGGGGTG others(331): Show |
1 | a0001c0004t0002g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.299-895_299-894ins others(338): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628320
|
A | G | 2 | a0002c0001t0015g0155a0002c0001t0057g0158 | 2 | HG01069.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.299-894T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628320 | ||||||
| chr19:1628321
|
C | CGGGGGTG others(61): Show |
1 | a0001c0004t0011g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.299-896_299-895ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628321 | ||||||
| chr19:1628321
|
C | CGGGGTGA others(162): Show |
1 | a0001c0005t0047g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.299-896_299-895ins others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628321 | ||||||
| chr19:1628321
|
CA | C | 36 | a0001c0002t0002g0188a0001c0002t0041g0004a0001c0002t0046g0039others(33): Show | 36 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.299-896delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628321 | ||||||
| chr19:1628321
|
CAG | C | 40 | a0001c0002t0001g0078a0001c0002t0001g0138a0001c0002t0001g0203others(37): Show | 40 | HG00438.hp2 HG00621.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.299-897_299-896del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628321 | ||||||
| chr19:1628321
|
CAGGGGAT others(202): Show |
C | 2 | a0001c0002t0001g0271a0001c0002t0002g0270 | 2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.299-1104_299-896de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628321 | ||||||
| chr19:1628321
|
CAGGGGAT others(444): Show |
C | 3 | a0001c0003t0001g0226a0001c0003t0001g0230a0001c0003t0002g0275 | 3 | HG00738.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.299-1346_299-896de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628321 | ||||||
| chr19:1628322
|
A | AGGGGGTG others(27): Show |
1 | a0001c0005t0017g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.299-897_299-896ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628322 | ||||||
| chr19:1628322
|
A | AGGGGGTG others(128): Show |
1 | a0001c0005t0009g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.299-897_299-896ins others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628322 | ||||||
| chr19:1628322
|
A | C | 1 | a0001c0005t0047g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.299-896T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628322 | ||||||
| chr19:1628322
|
A | G | 4 | a0001c0004t0021g0312a0001c0005t0001g0183a0003c0011t0030g0139others(1): Show | 4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-896T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628322 | ||||||
| chr19:1628322
|
A | T | 2 | a0001c0004t0003g0280a0001c0004t0011g0135 | 2 | HG00741.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.299-896T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628322 | ||||||
| chr19:1628323
|
G | C | 10 | a0001c0002t0002g0184a0001c0002t0005g0322a0001c0002t0085g0304others(7): Show | 10 | HG00738.hp1 HG01106.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-897C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628323
|
G | GGGGGTGA others(26): Show |
1 | a0001c0002t0013g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.299-898_299-897ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628323
|
G | GGGGGTGA others(26): Show |
4 | a0001c0004t0003g0153a0001c0004t0011g0136a0001c0004t0011g0137others(1): Show | 4 | HG01074.hp1 HG01257.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-898_299-897ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628323
|
G | GGGGGTGA others(95): Show |
1 | a0001c0004t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299-898_299-897ins others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628323
|
G | GGGGGTGA others(93): Show |
3 | a0002c0001t0014g0059a0002c0001t0053g0057a0002c0001t0095g0317 | 3 | HG02523.hp2 NA18948.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.299-898_299-897ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628323
|
G | T | 2 | a0004c0033t0036g0350a0005c0010t0018g0169 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299-897C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628323
|
GGGGATGA others(61): Show |
G | 2 | a0001c0003t0001g0227a0001c0003t0002g0001 | 3 | HG00280.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.299-965_299-898del others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628323
|
GGGGATGA others(541): Show |
G | 1 | a0001c0009t0098g0347 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.299-1445_299-898de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628323 | ||||||
| chr19:1628324
|
G | GGGGTGAG others(229): Show |
1 | a0002c0001t0007g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.299-899_299-898ins others(236): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628324 | ||||||
| chr19:1628325
|
G | C | 1 | a0001c0002t0083g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.299-899C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628325 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(300): Show |
1 | a0001c0002t0002g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.299-902_299-901ins others(307): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(742): Show |
1 | a0001c0005t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.299-902_299-901ins others(749): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(26): Show |
1 | a0018c0018t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-902_299-901ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(27): Show |
1 | a0003c0006t0001g0116 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.299-902_299-901ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(94): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-902_299-901ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(328): Show |
1 | a0001c0002t0002g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.299-902_299-901ins others(335): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(405): Show |
1 | a0003c0008t0068g0268 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.299-902_299-901ins others(412): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGCG others(26): Show |
1 | a0003c0011t0063g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.299-902_299-901ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | ATGAGGTG others(197): Show |
1 | a0001c0005t0027g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.299-902_299-901ins others(204): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628327
|
A | G | 216 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0138others(213): Show | 216 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.299-901T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628327 | ||||||
| chr19:1628330
|
A | AGGCGGGA others(191): Show |
1 | a0001c0002t0001g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-905_299-904ins others(198): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628330 | ||||||
| chr19:1628330
|
A | G | 8 | a0001c0003t0076g0045a0001c0004t0003g0280a0001c0004t0008g0248others(5): Show | 8 | HG00741.hp2 HG01109.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-904T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628330 | ||||||
| chr19:1628331
|
G | T | 3 | a0001c0004t0003g0099a0001c0004t0102g0344a0003c0006t0002g0123 | 3 | HG00408.hp2 HG00642.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.299-905C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628331 | ||||||
| chr19:1628333
|
C | A | 1 | a0001c0004t0011g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.299-907G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628333 | ||||||
| chr19:1628333
|
C | CGGGAAGG others(27): Show |
1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-908_299-907ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628333 | ||||||
| chr19:1628333
|
C | CGGGAAGG others(26): Show |
2 | a0001c0005t0038g0025a0002c0001t0007g0070 | 2 | NA18747.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.299-908_299-907ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628333 | ||||||
| chr19:1628333
|
C | T | 17 | a0001c0003t0002g0243a0001c0003t0028g0144a0001c0004t0002g0108others(14): Show | 17 | HG00438.hp2 HG00621.hp1 NA18522.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-907G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628333 | ||||||
| chr19:1628334
|
G | A | 2 | a0001c0004t0008g0248a0001c0004t0008g0252 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.299-908C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628334 | ||||||
| chr19:1628334
|
G | GGGAAGGG others(200): Show |
1 | a0001c0003t0001g0277 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.299-909_299-908ins others(207): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628334 | ||||||
| chr19:1628334
|
G | GGGAAGGG others(130): Show |
1 | a0001c0003t0002g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.299-909_299-908ins others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628334 | ||||||
| chr19:1628336
|
G | A | 5 | a0001c0003t0005g0325a0001c0007t0002g0127a0002c0001t0015g0081others(2): Show | 5 | HG01069.hp2 HG02004.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-910C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628336 | ||||||
| chr19:1628336
|
G | GAAGGGGA others(26): Show |
1 | a0001c0003t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.299-911_299-910ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628336 | ||||||
| chr19:1628339
|
G | A | 7 | a0001c0004t0001g0110a0001c0004t0002g0154a0001c0004t0008g0100others(4): Show | 7 | HG00597.hp2 HG01099.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-913C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628339 | ||||||
| chr19:1628347
|
C | T | 3 | a0001c0004t0066g0172a0001c0007t0002g0149a0003c0006t0002g0150 | 3 | HG02135.hp2 HG02300.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.299-921G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628347 | ||||||
| chr19:1628351
|
G | A | 32 | a0001c0002t0001g0218a0001c0002t0005g0330a0001c0002t0013g0197others(29): Show | 32 | HG00597.hp2 HG00609.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.299-925C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628351 | ||||||
| chr19:1628355
|
A | ACGGGGGG others(26): Show |
1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-930_299-929ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGGT others(25): Show |
1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-930_299-929ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGGT others(60): Show |
1 | a0001c0005t0025g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.299-930_299-929ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGGT others(59): Show |
1 | a0001c0005t0004g0027 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-930_299-929ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGGT others(58): Show |
5 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0216others(2): Show | 5 | HG01256.hp1 HG01433.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-930_299-929ins others(65): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGTG others(59): Show |
1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-930_299-929ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGTG others(93): Show |
3 | a0001c0005t0001g0207a0001c0005t0010g0117a0001c0005t0097g0320 | 3 | NA18986.hp1 NA19084.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.299-930_299-929ins others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGTG others(157): Show |
1 | a0001c0002t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.299-930_299-929ins others(164): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ACGGGGTG others(24): Show |
1 | a0003c0008t0101g0346 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.299-930_299-929ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ATGGGGGT others(125): Show |
1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-930_299-929ins others(132): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | ATGGGGTG others(91): Show |
1 | a0001c0004t0003g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.299-930_299-929ins others(98): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628355
|
A | G | 1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299-929T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628355 | ||||||
| chr19:1628356
|
C | CGGGGATG others(26): Show |
1 | a0001c0002t0041g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.299-931_299-930ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGGTG others(129): Show |
1 | a0001c0003t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-931_299-930ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGGTG others(26): Show |
2 | a0002c0001t0016g0052a0002c0001t0016g0269 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.299-931_299-930ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGGTG others(59): Show |
2 | a0001c0005t0009g0029a0002c0001t0007g0085 | 2 | HG00673.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.299-931_299-930ins others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGGTG others(26): Show |
1 | a0001c0003t0002g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.299-931_299-930ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGGTG others(60): Show |
1 | a0001c0003t0002g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.299-931_299-930ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGTGA others(25): Show |
1 | a0001c0002t0001g0213 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.299-931_299-930ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGTGA others(25): Show |
13 | a0001c0007t0002g0049a0002c0001t0006g0068a0002c0001t0007g0061others(10): Show | 13 | HG00609.hp2 HG01943.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-931_299-930ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGTGA others(703): Show |
1 | a0002c0001t0087g0291 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.299-931_299-930ins others(710): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
C | CGGGGTGA others(838): Show |
1 | a0002c0001t0014g0058 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.299-931_299-930ins others(845): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
CA | C | 45 | a0001c0002t0001g0138a0001c0002t0001g0180a0001c0002t0001g0203others(42): Show | 45 | HG00408.hp1 HG00621.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.299-931delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
CAG | C | 40 | a0001c0002t0001g0215a0001c0002t0001g0218a0001c0002t0002g0048others(37): Show | 40 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.299-932_299-931del others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
CAGGGGGT others(540): Show |
C | 3 | a0001c0003t0001g0228a0001c0003t0002g0274a0001c0003t0060g0273 | 3 | HG00639.hp2 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.299-1477_299-931de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628356
|
CAGGGGGT others(608): Show |
C | 1 | a0001c0004t0099g0343 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.299-1545_299-931de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628356 | ||||||
| chr19:1628357
|
A | AGGGGATG others(438): Show |
1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-932_299-931ins others(445): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628357 | ||||||
| chr19:1628357
|
A | AGGGGATG others(1098): Show |
1 | a0007c0016t0002g0260 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.299-932_299-931ins others(1105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628357 | ||||||
| chr19:1628357
|
A | AGGGGGTG others(504): Show |
1 | a0002c0001t0007g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-932_299-931ins others(511): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628357 | ||||||
| chr19:1628357
|
A | C | 10 | a0001c0002t0001g0213a0001c0002t0041g0004a0001c0003t0002g0094others(7): Show | 10 | HG00642.hp2 HG00673.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-931T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628357 | ||||||
| chr19:1628357
|
A | G | 1 | a0001c0005t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.299-931T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628357 | ||||||
| chr19:1628357
|
A | T | 14 | a0001c0007t0002g0049a0002c0001t0006g0068a0002c0001t0007g0061others(11): Show | 14 | HG00609.hp2 HG01943.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-931T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628357 | ||||||
| chr19:1628357
|
AG | A | 4 | a0001c0003t0001g0096a0001c0003t0002g0095a0001c0003t0002g0247others(1): Show | 4 | HG00741.hp1 HG01943.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-932delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628357 | ||||||
| chr19:1628358
|
G | C | 16 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(13): Show | 16 | HG01256.hp1 HG01433.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-932C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628358 | ||||||
| chr19:1628358
|
G | GGGGATGA others(734): Show |
1 | a0001c0002t0004g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-933_299-932ins others(741): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628358 | ||||||
| chr19:1628358
|
G | GGGGGTGA others(127): Show |
1 | a0001c0004t0003g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299-933_299-932ins others(134): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628358 | ||||||
| chr19:1628358
|
G | GGGGGTGA others(60): Show |
1 | a0001c0002t0002g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.299-933_299-932ins others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628358 | ||||||
| chr19:1628362
|
G | A | 37 | a0001c0002t0001g0111a0001c0002t0001g0178a0001c0002t0002g0188others(34): Show | 37 | HG00423.hp2 HG00544.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.299-936C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628362 | ||||||
| chr19:1628362
|
G | GTGAGGCG others(502): Show |
1 | a0001c0005t0004g0010 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299-937_299-936ins others(509): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628362 | ||||||
| chr19:1628365
|
A | AGGCGGGA others(62): Show |
2 | a0002c0001t0007g0060a0002c0001t0084g0290 | 2 | NA18990.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.299-940_299-939ins others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628365 | ||||||
| chr19:1628365
|
A | AGGTGGGA others(97): Show |
1 | a0001c0004t0003g0109 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.299-940_299-939ins others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628365 | ||||||
| chr19:1628365
|
A | AGGTGGGA others(62): Show |
1 | a0001c0002t0032g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-940_299-939ins others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628365 | ||||||
| chr19:1628365
|
A | G | 6 | a0001c0003t0002g0242a0001c0003t0002g0253a0001c0004t0003g0285others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-939T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628365 | ||||||
| chr19:1628366
|
G | C | 1 | a0005c0010t0018g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-940C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628366 | ||||||
| chr19:1628366
|
G | T | 1 | a0001c0004t0003g0099 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.299-940C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628366 | ||||||
| chr19:1628368
|
C | T | 11 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-942G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628368 | ||||||
| chr19:1628369
|
G | C | 1 | a0001c0003t0002g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.299-943C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628369 | ||||||
| chr19:1628369
|
GGGAAGGG others(199): Show |
G | 2 | a0001c0013t0037g0009a0003c0008t0001g0118 | 2 | HG02735.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.299-1149_299-944de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628369 | ||||||
| chr19:1628371
|
G | A | 1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299-945C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628371 | ||||||
| chr19:1628374
|
G | A | 20 | a0001c0003t0001g0096a0001c0003t0002g0094a0001c0003t0002g0095others(17): Show | 20 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-948C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628374 | ||||||
| chr19:1628374
|
G | GGGGACAG others(301): Show |
1 | a0001c0007t0012g0323 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.299-949_299-948ins others(308): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628374 | ||||||
| chr19:1628374
|
G | GGGGACAG others(61): Show |
1 | a0002c0001t0006g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.299-949_299-948ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628374 | ||||||
| chr19:1628374
|
G | GGGGACAG others(130): Show |
3 | a0003c0006t0010g0141a0003c0006t0017g0297a0003c0006t0033g0315 | 3 | NA18963.hp1 NA18989.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.299-949_299-948ins others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628374 | ||||||
| chr19:1628382
|
C | T | 1 | a0003c0006t0002g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.299-956G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628382 | ||||||
| chr19:1628386
|
A | ACTCACGG others(232): Show |
3 | a0003c0006t0001g0119a0003c0006t0002g0120a0003c0006t0080g0296 | 3 | NA18950.hp1 NA18970.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.299-961_299-960ins others(239): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628386 | ||||||
| chr19:1628386
|
A | G | 139 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(136): Show | 139 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.299-960T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628386 | ||||||
| chr19:1628388
|
T | TCG | 3 | a0002c0001t0014g0059a0002c0001t0053g0057a0002c0001t0095g0317 | 3 | HG02523.hp2 NA18948.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.299-963_299-962ins others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628388 | ||||||
| chr19:1628390
|
A | G | 1 | a0001c0004t0003g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-964T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628390 | ||||||
| chr19:1628391
|
C | CAG | 35 | a0001c0002t0001g0132a0001c0002t0001g0203a0001c0002t0002g0133others(32): Show | 35 | HG00438.hp2 HG00544.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.299-966_299-965ins others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGAT others(29): Show |
1 | a0001c0005t0025g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGAT others(64): Show |
1 | a0001c0005t0009g0022 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.299-966_299-965ins others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGAT others(750): Show |
1 | a0001c0003t0055g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(757): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGGT others(98): Show |
1 | a0001c0004t0003g0099 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGGT others(64): Show |
1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.299-966_299-965ins others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGGT others(29): Show |
1 | a0002c0001t0016g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.299-966_299-965ins others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGGT others(1813): Show |
1 | a0001c0003t0001g0233 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.299-966_299-965ins others(1820): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGTG others(744): Show |
1 | a0001c0025t0010g0266 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.299-966_299-965ins others(751): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGTG others(165): Show |
1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(172): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CAGGGGTG others(235): Show |
1 | a0001c0004t0008g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(242): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CG | 18 | a0001c0002t0078g0189a0001c0003t0002g0253a0001c0003t0028g0144others(15): Show | 18 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-966dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CGGGGGGT others(62): Show |
1 | a0001c0002t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.299-966_299-965ins others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CGGGGGTG others(95): Show |
1 | a0003c0006t0017g0294 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CGGGGGTG others(29): Show |
1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CGGGGTGA others(406): Show |
1 | a0001c0007t0091g0300 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(413): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CGGGGTGA others(336): Show |
1 | a0001c0007t0012g0335 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.299-966_299-965ins others(343): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | CGGGGTGA others(61): Show |
1 | a0003c0006t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-966_299-965ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | G | 4 | a0002c0001t0014g0059a0002c0001t0053g0057a0002c0001t0095g0317others(1): Show | 4 | HG02523.hp2 HG03927.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-965G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628391
|
C | T | 1 | a0001c0004t0011g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-965G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628391 | ||||||
| chr19:1628392
|
G | A | 1 | a0001c0009t0001g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.299-966C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628392 | ||||||
| chr19:1628392
|
GGGGTGAG others(505): Show |
G | 1 | a0001c0003t0001g0152 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.299-1478_299-967de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628392 | ||||||
| chr19:1628395
|
G | A | 7 | a0001c0003t0001g0261a0001c0003t0055g0235a0001c0003t0076g0045others(4): Show | 7 | HG01952.hp1 HG02004.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-969C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628395 | ||||||
| chr19:1628395
|
G | GTGAGGCG others(339): Show |
1 | a0001c0007t0090g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.299-970_299-969ins others(346): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628395 | ||||||
| chr19:1628398
|
A | AGGCGGGA others(92): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-973_299-972ins others(99): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628398 | ||||||
| chr19:1628398
|
A | AGGCGGGA others(61): Show |
1 | a0001c0004t0011g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.299-973_299-972ins others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628398 | ||||||
| chr19:1628398
|
A | G | 11 | a0001c0002t0001g0138a0001c0002t0001g0180a0001c0003t0002g0253others(8): Show | 11 | HG01109.hp2 HG01978.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-972T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628398 | ||||||
| chr19:1628399
|
G | T | 1 | a0001c0004t0003g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-973C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628399 | ||||||
| chr19:1628401
|
C | CGGGAAAG others(193): Show |
2 | a0001c0004t0001g0110a0001c0004t0002g0154 | 2 | HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.299-976_299-975ins others(200): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628401 | ||||||
| chr19:1628401
|
C | CGGGAAGG others(129): Show |
1 | a0001c0002t0041g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.299-976_299-975ins others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628401 | ||||||
| chr19:1628401
|
C | T | 21 | a0001c0002t0001g0218a0001c0002t0002g0190a0001c0003t0002g0243others(18): Show | 21 | HG00408.hp2 HG01069.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-975G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628401 | ||||||
| chr19:1628402
|
G | GGGAAGGG others(27): Show |
1 | a0001c0003t0009g0007 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.299-977_299-976ins others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628402 | ||||||
| chr19:1628402
|
G | GGGAAGGG others(196): Show |
1 | a0001c0007t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.299-977_299-976ins others(203): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628402 | ||||||
| chr19:1628404
|
G | A | 2 | a0003c0008t0082g0299a0003c0008t0101g0346 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.299-978C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628404 | ||||||
| chr19:1628407
|
G | A | 1 | a0003c0006t0002g0126 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.299-981C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628407 | ||||||
| chr19:1628414
|
G | C | 5 | a0001c0004t0003g0099a0001c0004t0008g0097a0001c0004t0008g0100others(2): Show | 5 | HG00639.hp1 HG00642.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-988C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628414 | ||||||
| chr19:1628415
|
C | CAGAACTC others(405): Show |
1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299-990_299-989ins others(412): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628415 | ||||||
| chr19:1628415
|
C | T | 3 | a0001c0002t0001g0173a0002c0001t0070g0121a0003c0006t0002g0150 | 3 | HG02135.hp2 NA18971.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.299-989G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628415 | ||||||
| chr19:1628419
|
G | A | 12 | a0001c0002t0001g0180a0001c0003t0077g0241a0001c0004t0003g0091others(9): Show | 12 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-993C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628419 | ||||||
| chr19:1628419
|
G | GCTCACAG others(133): Show |
1 | a0001c0004t0086g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.299-994_299-993ins others(140): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628419 | ||||||
| chr19:1628419
|
G | GCTCACGG others(94): Show |
1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.299-994_299-993ins others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628419 | ||||||
| chr19:1628419
|
GCTCACAG others(374): Show |
G | 1 | a0001c0003t0005g0326 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.299-1374_299-994de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628419 | ||||||
| chr19:1628423
|
A | ACGGGGAT others(25): Show |
1 | a0003c0006t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.299-998_299-997ins others(32): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | ACGGGGTG others(24): Show |
3 | a0001c0002t0001g0265a0001c0002t0002g0214a0001c0002t0002g0264 | 3 | HG01081.hp1 NA18970.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.299-998_299-997ins others(31): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | ACGGGGTG others(161): Show |
1 | a0001c0005t0009g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.299-998_299-997ins others(168): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | ACGGGGTG others(917): Show |
1 | a0019c0017t0001g0221 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.299-998_299-997ins others(924): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | ACGGGGTG others(160): Show |
1 | a0001c0003t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.299-998_299-997ins others(167): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | ACGGGGTG others(57): Show |
1 | a0001c0002t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299-998_299-997ins others(64): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | ACGGGGTG others(504): Show |
1 | a0001c0002t0036g0348 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-998_299-997ins others(511): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | ACGGGGTG others(123): Show |
2 | a0001c0002t0002g0267a0001c0002t0093g0341 | 2 | HG01192.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.299-998_299-997ins others(130): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
A | G | 3 | a0001c0004t0003g0220a0002c0001t0015g0155a0002c0001t0100g0342 | 3 | HG01243.hp2 HG01978.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.299-997T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628423
|
AC | A | 7 | a0001c0002t0001g0138a0001c0004t0003g0153a0001c0004t0011g0136others(4): Show | 7 | HG01175.hp1 HG01257.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-998delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628423 | ||||||
| chr19:1628424
|
C | CGGGGGTG others(26): Show |
1 | a0002c0001t0022g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-999_299-998ins others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628424 | ||||||
| chr19:1628424
|
CA | C | 34 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0078g0189others(31): Show | 35 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.299-999delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628424 | ||||||
| chr19:1628424
|
CAG | C | 37 | a0001c0002t0001g0215a0001c0002t0002g0143a0001c0002t0002g0188others(34): Show | 37 | HG00438.hp2 HG00735.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.299-1000_299-999de others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628424 | ||||||
| chr19:1628424
|
CAGGGGGT others(29): Show |
C | 1 | a0001c0005t0004g0031 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.299-1034_299-999de others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628424 | ||||||
| chr19:1628424
|
CAGGGGGT others(65): Show |
C | 1 | a0001c0009t0050g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-1070_299-999de others(73): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628424 | ||||||
| chr19:1628424
|
CAGGGGGT others(271): Show |
C | 1 | a0001c0002t0013g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.299-1276_299-999de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628424 | ||||||
| chr19:1628424
|
CAGGGGGT others(505): Show |
C | 1 | a0001c0003t0028g0144 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.299-1510_299-999de others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628424 | ||||||
| chr19:1628425
|
A | C | 1 | a0002c0001t0022g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-999T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628425 | ||||||
| chr19:1628425
|
A | G | 2 | a0001c0007t0001g0238a0005c0010t0018g0171 | 2 | HG02559.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.299-999T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628425 | ||||||
| chr19:1628425
|
A | T | 7 | a0001c0002t0001g0138a0001c0004t0003g0153a0001c0004t0011g0136others(4): Show | 7 | HG01175.hp1 HG01257.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-999T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628425 | ||||||
| chr19:1628426
|
G | C | 11 | a0001c0002t0001g0180a0001c0002t0001g0265a0001c0002t0002g0214others(8): Show | 11 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-1000C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628426 | ||||||
| chr19:1628426
|
G | GGGGGTGA others(26): Show |
1 | a0003c0006t0012g0314 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.299-1001_299-1000i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628426 | ||||||
| chr19:1628426
|
G | GGGGGTGA others(26): Show |
2 | a0001c0004t0008g0248a0001c0004t0008g0252 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.299-1001_299-1000i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628426 | ||||||
| chr19:1628426
|
G | GGGGGTGA others(61): Show |
1 | a0001c0005t0004g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.299-1001_299-1000i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628426 | ||||||
| chr19:1628426
|
G | GGGGGTGA others(60): Show |
1 | a0002c0001t0007g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.299-1001_299-1000i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628426 | ||||||
| chr19:1628426
|
G | GGGGGTGA others(95): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-1001_299-1000i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628426 | ||||||
| chr19:1628426
|
G | T | 1 | a0001c0002t0002g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.299-1000C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628426 | ||||||
| chr19:1628430
|
G | A | 36 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0138others(33): Show | 36 | HG00597.hp2 HG00609.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.299-1004C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628430 | ||||||
| chr19:1628432
|
G | A | 1 | a0001c0002t0002g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.299-1006C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628432 | ||||||
| chr19:1628433
|
A | AGGCGGGA others(161): Show |
1 | a0002c0001t0007g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.299-1008_299-1007i others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628433 | ||||||
| chr19:1628433
|
A | G | 20 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0002g0133others(17): Show | 20 | HG00609.hp2 HG01257.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-1007T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628433 | ||||||
| chr19:1628434
|
G | T | 11 | a0001c0004t0003g0099a0001c0004t0003g0220a0001c0004t0008g0097others(8): Show | 11 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-1008C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628434 | ||||||
| chr19:1628436
|
C | CGGGAAGG others(26): Show |
1 | a0001c0005t0009g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.299-1011_299-1010i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628436 | ||||||
| chr19:1628436
|
C | T | 17 | a0001c0002t0001g0111a0001c0002t0001g0181a0001c0002t0032g0161others(14): Show | 17 | HG00140.hp2 HG00735.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-1010G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628436 | ||||||
| chr19:1628437
|
G | A | 2 | a0004c0033t0036g0350a0005c0010t0018g0169 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299-1011C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628437 | ||||||
| chr19:1628437
|
G | GGGAAGGG others(272): Show |
1 | a0001c0005t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.299-1012_299-1011i others(281): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628437 | ||||||
| chr19:1628439
|
A | AAAGGGGA others(434): Show |
1 | a0001c0003t0089g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-1014_299-1013i others(443): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628439 | ||||||
| chr19:1628439
|
A | AAAGGGGA others(266): Show |
1 | a0001c0007t0002g0278 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.299-1014_299-1013i others(275): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628439 | ||||||
| chr19:1628439
|
A | AAAGGGGA others(26): Show |
1 | a0001c0004t0008g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-1014_299-1013i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628439 | ||||||
| chr19:1628439
|
A | G | 281 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(278): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.299-1013T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628439 | ||||||
| chr19:1628442
|
G | A | 6 | a0001c0002t0036g0348a0001c0003t0001g0227a0001c0003t0002g0001others(3): Show | 7 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-1016C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628442 | ||||||
| chr19:1628442
|
G | GGGGACAG others(96): Show |
1 | a0014c0020t0034g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.299-1017_299-1016i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628442 | ||||||
| chr19:1628442
|
G | GGGGACAG others(261): Show |
1 | a0001c0002t0001g0203 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.299-1017_299-1016i others(270): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628442 | ||||||
| chr19:1628449
|
G | C | 3 | a0001c0003t0008g0098a0001c0004t0008g0100a0002c0001t0001g0122 | 3 | HG00280.hp2 HG01099.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.299-1023C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628449 | ||||||
| chr19:1628449
|
G | GCAGAGCT others(162): Show |
2 | a0001c0003t0001g0096a0001c0003t0002g0247 | 2 | HG01943.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.299-1024_299-1023i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628449 | ||||||
| chr19:1628449
|
G | GCAGAGCT others(60): Show |
1 | a0003c0006t0001g0116 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.299-1024_299-1023i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628449 | ||||||
| chr19:1628450
|
C | T | 3 | a0001c0007t0002g0127a0003c0006t0002g0150a0003c0008t0068g0268 | 3 | HG00323.hp1 HG02071.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.299-1024G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628450 | ||||||
| chr19:1628454
|
G | A | 16 | a0001c0002t0001g0078a0001c0002t0002g0190a0001c0002t0004g0012others(13): Show | 16 | HG00609.hp1 HG01175.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-1028C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628454 | ||||||
| chr19:1628454
|
G | GCTCACGG others(93): Show |
1 | a0002c0001t0006g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.299-1029_299-1028i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628454 | ||||||
| chr19:1628458
|
A | ACAGGGGG others(168): Show |
1 | a0001c0004t0003g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-1033_299-1032i others(177): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGGT others(25): Show |
1 | a0003c0006t0035g0345 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.299-1033_299-1032i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGGT others(127): Show |
1 | a0002c0001t0022g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.299-1033_299-1032i others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGGT others(327): Show |
1 | a0002c0001t0015g0080 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-1033_299-1032i others(336): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGGT others(25): Show |
2 | a0002c0001t0014g0059a0002c0001t0095g0317 | 2 | HG02523.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.299-1033_299-1032i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGGT others(230): Show |
1 | a0001c0004t0003g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-1033_299-1032i others(239): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGTG others(24): Show |
1 | a0001c0019t0026g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.299-1033_299-1032i others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGTG others(24): Show |
1 | a0001c0002t0001g0213 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.299-1033_299-1032i others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGTG others(839): Show |
1 | a0003c0006t0001g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.299-1033_299-1032i others(848): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGTG others(57): Show |
1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-1033_299-1032i others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ACGGGGTG others(160): Show |
1 | a0001c0005t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.299-1033_299-1032i others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | ATGGGGGT others(95): Show |
2 | a0002c0001t0073g0079a0002c0001t0092g0295 | 2 | NA18947.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.299-1033_299-1032i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628458
|
A | G | 16 | a0001c0004t0021g0321a0001c0007t0002g0049a0002c0001t0006g0068others(13): Show | 16 | HG00609.hp2 HG01069.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-1032T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628458 | ||||||
| chr19:1628459
|
C | CGGGGGTG others(61): Show |
1 | a0001c0004t0002g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-1034_299-1033i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628459
|
C | CGGGGGTG others(60): Show |
1 | a0001c0004t0003g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-1034_299-1033i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628459
|
C | CGGGGTGA others(159): Show |
1 | a0002c0001t0029g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.299-1034_299-1033i others(168): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628459
|
CA | C | 38 | a0001c0002t0001g0138a0001c0002t0001g0218a0001c0002t0002g0143others(35): Show | 38 | HG00673.hp1 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.299-1034delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628459
|
CAG | C | 42 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0173others(39): Show | 42 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.299-1035_299-1034d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628459
|
CAGGGGAT others(31): Show |
C | 1 | a0001c0009t0001g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.299-1071_299-1034d others(40): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628459
|
CAGGGGAT others(64): Show |
C | 1 | a0001c0007t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.299-1104_299-1034d others(73): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628459
|
CAGGGGAT others(306): Show |
C | 1 | a0001c0009t0049g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.299-1346_299-1034d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628459 | ||||||
| chr19:1628460
|
A | AGGGGGTG others(1873): Show |
1 | a0001c0003t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.299-1035_299-1034i others(1882): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628460 | ||||||
| chr19:1628460
|
A | AGGGGGTG others(96): Show |
1 | a0009c0021t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299-1035_299-1034i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628460 | ||||||
| chr19:1628460
|
A | C | 2 | a0001c0004t0002g0257a0002c0001t0029g0159 | 2 | HG00738.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.299-1034T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628460 | ||||||
| chr19:1628460
|
A | G | 1 | a0002c0001t0006g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.299-1034T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628460 | ||||||
| chr19:1628460
|
A | T | 3 | a0001c0004t0003g0104a0001c0004t0003g0280a0001c0007t0103g0351 | 3 | HG02258.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.299-1034T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628460 | ||||||
| chr19:1628461
|
G | C | 11 | a0001c0002t0001g0213a0001c0004t0003g0285a0001c0005t0001g0183others(8): Show | 11 | HG00597.hp2 HG01358.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-1035C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628461 | ||||||
| chr19:1628461
|
G | GGGGGTGA others(26): Show |
1 | a0001c0002t0002g0222 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.299-1036_299-1035i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628461 | ||||||
| chr19:1628461
|
G | GGGGGTGA others(60): Show |
1 | a0001c0002t0002g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-1036_299-1035i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628461 | ||||||
| chr19:1628461
|
G | GGGGGTGA others(127): Show |
1 | a0002c0001t0007g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.299-1036_299-1035i others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628461 | ||||||
| chr19:1628461
|
G | GGGGGTGA others(300): Show |
1 | a0001c0003t0005g0338 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.299-1036_299-1035i others(309): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628461 | ||||||
| chr19:1628461
|
G | GGGGGTGA others(96): Show |
1 | a0001c0004t0008g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.299-1036_299-1035i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628461 | ||||||
| chr19:1628464
|
GA | G | 4 | a0001c0003t0002g0095a0001c0004t0003g0047a0002c0001t0006g0055others(1): Show | 4 | HG00741.hp1 HG01978.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1039delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628464 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(26): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-1040_299-1039i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(94): Show |
1 | a0001c0003t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.299-1040_299-1039i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(28): Show |
1 | a0001c0003t0002g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.299-1074_299-1040d others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(61): Show |
1 | a0001c0002t0005g0322 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.299-1040_299-1039i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(407): Show |
1 | a0001c0003t0005g0336 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.299-1040_299-1039i others(416): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(507): Show |
1 | a0001c0003t0002g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.299-1040_299-1039i others(516): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(60): Show |
1 | a0001c0005t0047g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.299-1040_299-1039i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | ATGAGGCG others(96): Show |
2 | a0001c0003t0001g0234a0001c0003t0005g0340 | 2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.299-1040_299-1039i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628465
|
A | G | 220 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(217): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.299-1039T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628465 | ||||||
| chr19:1628468
|
A | AGGCGGAA others(27): Show |
1 | a0002c0001t0034g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.299-1043_299-1042i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628468 | ||||||
| chr19:1628468
|
A | AGGCGGGA others(989): Show |
1 | a0001c0007t0002g0259 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.299-1043_299-1042i others(998): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628468 | ||||||
| chr19:1628468
|
A | G | 17 | a0001c0002t0001g0138a0001c0002t0001g0173a0001c0003t0001g0255others(14): Show | 17 | HG01168.hp2 HG01257.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-1042T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628468 | ||||||
| chr19:1628469
|
G | T | 5 | a0001c0003t0001g0096a0001c0003t0002g0247a0001c0003t0008g0098others(2): Show | 5 | HG00280.hp2 HG01943.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1043C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628469 | ||||||
| chr19:1628471
|
C | T | 13 | a0001c0002t0032g0161a0001c0003t0002g0094a0001c0004t0003g0105others(10): Show | 13 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-1045G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628471 | ||||||
| chr19:1628472
|
G | GGGAAAGG others(61): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-1047_299-1046i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628472 | ||||||
| chr19:1628474
|
G | A | 23 | a0001c0004t0008g0248a0001c0004t0008g0252a0001c0007t0002g0049others(20): Show | 23 | HG00609.hp2 HG01069.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.299-1048C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628474 | ||||||
| chr19:1628477
|
G | A | 9 | a0001c0003t0005g0331a0001c0004t0001g0110a0001c0004t0002g0154others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-1051C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628477 | ||||||
| chr19:1628484
|
G | C | 2 | a0001c0007t0002g0282a0001c0025t0010g0266 | 2 | NA18906.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.299-1058C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628484 | ||||||
| chr19:1628485
|
C | CAGAGCTC others(26): Show |
1 | a0001c0005t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.299-1060_299-1059i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628485 | ||||||
| chr19:1628485
|
C | T | 5 | a0001c0007t0002g0127a0001c0007t0012g0323a0003c0006t0002g0077others(2): Show | 5 | HG00323.hp1 HG00558.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1059G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628485 | ||||||
| chr19:1628489
|
G | A | 32 | a0001c0002t0001g0203a0001c0002t0004g0012a0001c0002t0041g0004others(29): Show | 32 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.299-1063C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628489 | ||||||
| chr19:1628489
|
G | GCTCACGG others(266): Show |
1 | a0001c0005t0017g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.299-1064_299-1063i others(275): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628489 | ||||||
| chr19:1628493
|
A | ACGGGGAT others(25): Show |
1 | a0001c0003t0005g0325 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.299-1068_299-1067i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGGT others(25): Show |
1 | a0002c0001t0007g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.299-1068_299-1067i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGGT others(534): Show |
1 | a0002c0001t0019g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.299-1068_299-1067i others(543): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGGT others(229): Show |
1 | a0002c0001t0054g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.299-1068_299-1067i others(238): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGGT others(367): Show |
1 | a0001c0002t0002g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-1068_299-1067i others(376): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(24): Show |
1 | a0002c0001t0015g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-1068_299-1067i others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(24): Show |
1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.299-1068_299-1067i others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(94): Show |
1 | a0001c0007t0003g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-1068_299-1067i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(59): Show |
1 | a0001c0005t0004g0027 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.299-1068_299-1067i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(333): Show |
1 | a0003c0006t0010g0124 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.299-1068_299-1067i others(342): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(58): Show |
1 | a0001c0003t0010g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.299-1068_299-1067i others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(190): Show |
1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-1068_299-1067i others(199): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ACGGGGTG others(332): Show |
1 | a0001c0004t0008g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.299-1068_299-1067i others(341): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | ATGGGGGT others(194): Show |
1 | a0001c0007t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-1068_299-1067i others(203): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628493
|
A | G | 2 | a0001c0004t0021g0321a0002c0001t0087g0291 | 2 | HG03516.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.299-1067T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628493 | ||||||
| chr19:1628494
|
C | CGGGGGTG others(92): Show |
1 | a0002c0001t0022g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-1069_299-1068i others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628494 | ||||||
| chr19:1628494
|
CA | C | 38 | a0001c0002t0001g0138a0001c0002t0001g0174a0001c0002t0001g0215others(35): Show | 38 | HG00423.hp2 HG00609.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.299-1069delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628494 | ||||||
| chr19:1628494
|
CAG | C | 64 | a0001c0002t0001g0132a0001c0002t0001g0203a0001c0002t0001g0209others(61): Show | 64 | HG00408.hp1 HG00673.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.299-1070_299-1069d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628494 | ||||||
| chr19:1628494
|
CAGGGGGT others(97): Show |
C | 1 | a0001c0004t0028g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.299-1172_299-1069d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628494 | ||||||
| chr19:1628495
|
A | AGGGGATG others(128): Show |
1 | a0001c0003t0002g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.299-1070_299-1069i others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628495 | ||||||
| chr19:1628495
|
A | AGGGGATG others(127): Show |
1 | a0003c0006t0001g0125 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.299-1070_299-1069i others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628495 | ||||||
| chr19:1628495
|
A | C | 1 | a0002c0001t0022g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-1069T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628495 | ||||||
| chr19:1628495
|
A | G | 8 | a0001c0002t0002g0186a0001c0004t0003g0104a0001c0005t0001g0183others(5): Show | 8 | HG02523.hp2 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-1069T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628495 | ||||||
| chr19:1628495
|
A | T | 1 | a0001c0004t0003g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.299-1069T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628495 | ||||||
| chr19:1628495
|
AG | A | 5 | a0001c0002t0032g0161a0001c0004t0003g0105a0001c0004t0003g0106others(2): Show | 5 | HG00735.hp2 HG01123.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1070delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628495 | ||||||
| chr19:1628496
|
G | C | 14 | a0001c0002t0002g0175a0001c0002t0002g0184a0001c0003t0005g0325others(11): Show | 14 | HG01255.hp1 HG02004.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-1070C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628496 | ||||||
| chr19:1628496
|
G | GGGGATGA others(26): Show |
1 | a0001c0002t0046g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.299-1071_299-1070i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628496 | ||||||
| chr19:1628496
|
G | GGGGATGA others(129): Show |
1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.299-1071_299-1070i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628496 | ||||||
| chr19:1628496
|
G | GGGGATGA others(95): Show |
1 | a0001c0005t0004g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.299-1071_299-1070i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628496 | ||||||
| chr19:1628496
|
G | GGGGTGAG others(298): Show |
1 | a0003c0006t0031g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.299-1071_299-1070i others(307): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628496 | ||||||
| chr19:1628496
|
G | T | 1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-1070C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628496 | ||||||
| chr19:1628497
|
G | A | 1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-1071C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628497 | ||||||
| chr19:1628500
|
G | A | 32 | a0001c0002t0001g0173a0001c0002t0002g0188a0001c0002t0002g0191others(29): Show | 32 | HG00438.hp2 HG01069.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.299-1074C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628500 | ||||||
| chr19:1628502
|
G | A | 1 | a0002c0001t0006g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.299-1076C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628502 | ||||||
| chr19:1628503
|
A | G | 28 | a0001c0002t0001g0138a0001c0002t0032g0161a0001c0002t0058g0283others(25): Show | 28 | HG00609.hp2 HG00735.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.299-1077T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628503 | ||||||
| chr19:1628504
|
G | T | 4 | a0001c0003t0008g0098a0003c0006t0001g0142a0003c0008t0082g0299others(1): Show | 4 | HG00280.hp2 HG02738.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1078C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628504 | ||||||
| chr19:1628506
|
C | CGGGAAGG others(60): Show |
1 | a0002c0001t0006g0072 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.299-1081_299-1080i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628506 | ||||||
| chr19:1628506
|
C | T | 11 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0075g0185others(8): Show | 11 | HG01074.hp1 HG01106.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-1080G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628506 | ||||||
| chr19:1628509
|
G | A | 3 | a0001c0003t0002g0258a0001c0007t0090g0306a0002c0001t0087g0291 | 3 | HG02129.hp2 HG02523.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.299-1083C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628509 | ||||||
| chr19:1628512
|
G | A | 8 | a0001c0003t0001g0096a0001c0003t0002g0247a0001c0004t0002g0108others(5): Show | 8 | HG01943.hp2 HG01978.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1086C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628512 | ||||||
| chr19:1628519
|
G | C | 1 | a0001c0003t0005g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-1093C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628519 | ||||||
| chr19:1628520
|
C | A | 1 | a0003c0006t0017g0294 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.299-1094G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628520 | ||||||
| chr19:1628520
|
C | T | 7 | a0001c0007t0012g0323a0002c0001t0001g0122a0003c0006t0001g0125others(4): Show | 7 | HG00323.hp1 HG00558.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-1094G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628520 | ||||||
| chr19:1628524
|
G | A | 43 | a0001c0002t0001g0111a0001c0002t0001g0181a0001c0002t0004g0012others(40): Show | 43 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.299-1098C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628524 | ||||||
| chr19:1628524
|
G | GCTCACAG others(28): Show |
1 | a0020c0034t0010g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.299-1099_299-1098i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628524 | ||||||
| chr19:1628528
|
A | G | 3 | a0001c0007t0074g0090a0001c0007t0096g0311a0002c0001t0014g0058 | 3 | HG03490.hp1 HG03492.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.299-1102T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628528 | ||||||
| chr19:1628529
|
C | CA | 78 | a0001c0002t0001g0180a0001c0002t0002g0048a0001c0002t0002g0175others(75): Show | 78 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.299-1104_299-1103i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CAGGGGAT others(264): Show |
1 | a0001c0005t0026g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299-1104_299-1103i others(273): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CAGGGGGT others(303): Show |
1 | a0001c0003t0009g0007 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.299-1104_299-1103i others(312): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CAGGGGGT others(1407): Show |
1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-1104_299-1103i others(1416): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CGGGGTGA others(27): Show |
2 | a0001c0005t0024g0002a0001c0005t0024g0003 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.299-1104_299-1103i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CGGGGTGA others(27): Show |
1 | a0001c0005t0004g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.299-1104_299-1103i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CGGGGTGA others(1288): Show |
1 | a0001c0005t0004g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.299-1104_299-1103i others(1297): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CGGGGTGA others(295): Show |
1 | a0001c0002t0001g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-1104_299-1103i others(304): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CGGGGTGA others(128): Show |
1 | a0003c0006t0033g0315 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.299-1104_299-1103i others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | CGGGGTGA others(335): Show |
2 | a0003c0006t0002g0123a0003c0006t0017g0297 | 2 | NA18989.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.299-1104_299-1103i others(344): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
C | T | 13 | a0001c0002t0001g0138a0001c0002t0032g0161a0001c0003t0002g0095others(10): Show | 13 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-1103G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
CG | C | 79 | a0001c0002t0001g0198a0001c0002t0001g0215a0001c0002t0001g0218others(76): Show | 79 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.299-1104delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628529
|
CGGGGGTG others(63): Show |
C | 1 | a0001c0003t0077g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.299-1173_299-1104d others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628529 | ||||||
| chr19:1628530
|
G | A | 4 | a0001c0004t0003g0104a0002c0001t0006g0055a0002c0001t0019g0056others(1): Show | 4 | HG00544.hp1 HG02922.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1104C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | C | 2 | a0001c0003t0009g0007a0001c0005t0026g0037 | 2 | HG01256.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.299-1104C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGATGG others(26): Show |
1 | a0003c0006t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.299-1105_299-1104i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGGTGA others(196): Show |
1 | a0004c0014t0079g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.299-1105_299-1104i others(205): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(59): Show |
1 | a0001c0003t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-1105_299-1104i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(159): Show |
1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-1105_299-1104i others(168): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(264): Show |
1 | a0001c0005t0009g0013 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.299-1105_299-1104i others(273): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(93): Show |
1 | a0001c0002t0004g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-1105_299-1104i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(329): Show |
2 | a0001c0005t0009g0024a0001c0005t0044g0041 | 2 | NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.299-1105_299-1104i others(338): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(396): Show |
1 | a0001c0002t0085g0304 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.299-1105_299-1104i others(405): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(257): Show |
1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-1105_299-1104i others(266): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(59): Show |
2 | a0002c0001t0006g0063a0002c0001t0007g0064 | 2 | NA19066.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.299-1105_299-1104i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
G | GGGGTGAG others(259): Show |
1 | a0002c0001t0057g0158 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.299-1105_299-1104i others(268): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628530
|
GGGGGTGA others(268): Show |
G | 1 | a0001c0003t0001g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.299-1379_299-1105d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628530 | ||||||
| chr19:1628531
|
G | A | 1 | a0016c0027t0004g0020 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.299-1105C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628531 | ||||||
| chr19:1628534
|
G | A | 22 | a0001c0002t0001g0138a0001c0002t0002g0175a0001c0002t0032g0161others(19): Show | 22 | HG00423.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-1108C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628534 | ||||||
| chr19:1628534
|
G | GTGAGGCG others(28): Show |
1 | a0001c0004t0003g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-1109_299-1108i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628534 | ||||||
| chr19:1628534
|
GTGAGGCG others(165): Show |
G | 1 | a0001c0003t0002g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.299-1280_299-1109d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628534 | ||||||
| chr19:1628537
|
A | G | 24 | a0001c0002t0001g0138a0001c0002t0032g0161a0001c0003t0002g0095others(21): Show | 24 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.299-1111T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628537 | ||||||
| chr19:1628540
|
C | CGGGAAGG others(196): Show |
3 | a0001c0004t0003g0153a0001c0004t0011g0136a0001c0004t0081g0302 | 3 | HG01257.hp2 HG01975.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.299-1115_299-1114i others(205): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628540 | ||||||
| chr19:1628540
|
C | CGGGAAGG others(725): Show |
1 | a0001c0004t0021g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.299-1115_299-1114i others(734): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628540 | ||||||
| chr19:1628540
|
C | CGGGAAGG others(1663): Show |
1 | a0001c0004t0003g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.299-1115_299-1114i others(1672): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628540 | ||||||
| chr19:1628540
|
C | T | 11 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0004t0001g0110others(8): Show | 11 | HG01069.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-1114G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628540 | ||||||
| chr19:1628541
|
GGGAAGGG others(27): Show |
G | 2 | a0001c0004t0011g0102a0001c0005t0004g0031 | 2 | NA19000.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.299-1149_299-1116d others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628541 | ||||||
| chr19:1628543
|
G | A | 3 | a0001c0007t0074g0090a0001c0007t0096g0311a0002c0001t0014g0058 | 3 | HG03490.hp1 HG03492.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.299-1117C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628543 | ||||||
| chr19:1628544
|
A | G | 1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-1118T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628544 | ||||||
| chr19:1628546
|
G | A | 1 | a0003c0006t0012g0313 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.299-1120C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628546 | ||||||
| chr19:1628553
|
G | C | 1 | a0001c0007t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.299-1127C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628553 | ||||||
| chr19:1628554
|
C | T | 12 | a0001c0005t0009g0018a0001c0007t0002g0149a0001c0007t0012g0323others(9): Show | 12 | HG00323.hp1 HG01123.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-1128G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628554 | ||||||
| chr19:1628558
|
G | A | 31 | a0001c0002t0002g0191a0001c0002t0002g0202a0001c0004t0003g0109others(28): Show | 31 | HG00544.hp1 HG00642.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.299-1132C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628558 | ||||||
| chr19:1628563
|
C | CA | 71 | a0001c0002t0001g0138a0001c0002t0001g0178a0001c0002t0002g0048others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.299-1138_299-1137i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CAGGGGAT others(543): Show |
1 | a0001c0004t0003g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-1138_299-1137i others(552): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CAGGGGGT others(62): Show |
1 | a0001c0002t0013g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CAGGGGGT others(131): Show |
1 | a0003c0008t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-1138_299-1137i others(140): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CAGGGGGT others(96): Show |
1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-1138_299-1137i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CAGGGGGT others(62): Show |
1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CG | 11 | a0001c0007t0002g0049a0002c0001t0006g0068a0002c0001t0007g0065others(8): Show | 11 | HG00609.hp2 HG01943.hp1 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-1138dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGATG others(28): Show |
1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGGTG others(129): Show |
1 | a0003c0006t0002g0077 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGTGA others(373): Show |
1 | a0004c0014t0013g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.299-1138_299-1137i others(382): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGTGA others(266): Show |
1 | a0001c0004t0008g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(275): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGTGA others(27): Show |
1 | a0001c0003t0005g0338 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGTGA others(438): Show |
1 | a0001c0004t0008g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(447): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGTGA others(27): Show |
1 | a0002c0001t0034g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGTGA others(27): Show |
1 | a0001c0005t0009g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.299-1138_299-1137i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | CGGGGTGA others(129): Show |
1 | a0001c0004t0002g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.299-1138_299-1137i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
C | T | 6 | a0001c0004t0003g0104a0001c0004t0003g0280a0001c0007t0003g0107others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1137G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
CG | C | 76 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0173others(73): Show | 76 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.299-1138delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628563
|
CGGGGGTG others(236): Show |
C | 1 | a0001c0007t0103g0351 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.299-1380_299-1138d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628563 | ||||||
| chr19:1628564
|
G | A | 3 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0003t0002g0094 | 3 | HG02602.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.299-1138C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | C | 1 | a0001c0002t0013g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.299-1138C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | GGGGTAAG others(25): Show |
1 | a0001c0002t0002g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.299-1139_299-1138i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | GGGGTGAG others(25): Show |
3 | a0001c0002t0075g0185a0001c0005t0001g0208a0009c0021t0001g0254 | 3 | HG03453.hp1 HG03579.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.299-1139_299-1138i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | GGGGTGAG others(161): Show |
1 | a0001c0003t0002g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.299-1139_299-1138i others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | GGGGTGAG others(91): Show |
5 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0216others(2): Show | 5 | HG01256.hp1 HG01433.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1139_299-1138i others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | GGGGTGAG others(91): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-1139_299-1138i others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | GGGGTGAG others(292): Show |
1 | a0001c0002t0005g0328 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.299-1139_299-1138i others(301): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628564
|
G | GGGGTGAG others(965): Show |
1 | a0001c0002t0093g0341 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.299-1139_299-1138i others(974): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628564 | ||||||
| chr19:1628568
|
G | A | 40 | a0001c0002t0001g0178a0001c0002t0005g0319a0001c0002t0035g0349others(37): Show | 40 | HG00323.hp2 HG00438.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.299-1142C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628568 | ||||||
| chr19:1628570
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.299-1144C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628570 | ||||||
| chr19:1628571
|
G | A | 226 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0138others(223): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.299-1145C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628571 | ||||||
| chr19:1628571
|
G | GGGCGGGA others(228): Show |
1 | a0002c0001t0029g0156 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.299-1146_299-1145i others(237): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628571 | ||||||
| chr19:1628571
|
GGGCAGGA others(234): Show |
G | 1 | a0002c0001t0070g0121 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.299-1386_299-1146d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628571 | ||||||
| chr19:1628572
|
G | GGCGGGAA others(163): Show |
1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-1147_299-1146i others(172): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628572 | ||||||
| chr19:1628572
|
G | T | 3 | a0003c0006t0001g0116a0003c0006t0067g0130a0003c0008t0001g0113 | 3 | HG02723.hp1 HG03704.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.299-1146C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628572 | ||||||
| chr19:1628574
|
C | CGGGAAGG others(94): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-1149_299-1148i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628574 | ||||||
| chr19:1628574
|
C | T | 16 | a0001c0002t0005g0319a0001c0004t0001g0110a0001c0004t0002g0154others(13): Show | 16 | HG00544.hp1 HG00642.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-1148G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628574 | ||||||
| chr19:1628575
|
A | G | 282 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(279): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.299-1149T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628575 | ||||||
| chr19:1628577
|
G | A | 2 | a0001c0007t0012g0323a0003c0006t0002g0126 | 2 | HG00438.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.299-1151C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628577 | ||||||
| chr19:1628580
|
G | A | 3 | a0001c0002t0001g0138a0001c0002t0078g0189a0003c0006t0035g0345 | 3 | HG00597.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.299-1154C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628580 | ||||||
| chr19:1628580
|
G | GGGGACAG others(166): Show |
1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-1155_299-1154i others(175): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628580 | ||||||
| chr19:1628588
|
C | CAGAGCTC others(61): Show |
1 | a0014c0020t0034g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.299-1163_299-1162i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628588 | ||||||
| chr19:1628588
|
C | T | 10 | a0001c0007t0002g0127a0001c0009t0050g0168a0001c0025t0010g0266others(7): Show | 10 | HG00544.hp1 HG02071.hp1 HG03579.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-1162G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628588 | ||||||
| chr19:1628592
|
G | A | 27 | a0001c0002t0001g0138a0001c0002t0036g0348a0001c0002t0041g0004others(24): Show | 27 | HG00438.hp2 HG00597.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.299-1166C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628592 | ||||||
| chr19:1628592
|
G | GCTCACGG others(94): Show |
1 | a0001c0019t0026g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.299-1167_299-1166i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628592 | ||||||
| chr19:1628596
|
A | ACGGGGGT others(129): Show |
2 | a0001c0004t0003g0105a0001c0004t0011g0145 | 2 | HG00735.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.299-1171_299-1170i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ACGGGGTG others(59): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-1171_299-1170i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ACGGGGTG others(260): Show |
1 | a0002c0001t0006g0055 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.299-1171_299-1170i others(269): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ACGGGGTG others(93): Show |
1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.299-1171_299-1170i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ACGGGGTG others(57): Show |
1 | a0001c0002t0083g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.299-1171_299-1170i others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ACGGGGTG others(57): Show |
2 | a0001c0002t0001g0265a0001c0002t0002g0264 | 2 | NA18970.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.299-1171_299-1170i others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ACGGGGTG others(125): Show |
1 | a0001c0005t0038g0025 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.299-1171_299-1170i others(134): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ACGGGGTG others(424): Show |
1 | a0001c0002t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299-1171_299-1170i others(433): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ATGGGGAT others(467): Show |
2 | a0001c0002t0001g0132a0001c0002t0002g0133 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.299-1171_299-1170i others(476): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | ATGGGGGG others(229): Show |
1 | a0001c0002t0032g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-1171_299-1170i others(238): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
A | G | 2 | a0002c0001t0015g0080a0004c0014t0079g0305 | 2 | HG01358.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.299-1170T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628596
|
AC | A | 6 | a0002c0001t0006g0067a0002c0001t0007g0069a0002c0001t0007g0070others(3): Show | 6 | HG00673.hp1 HG03017.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-1171delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628596 | ||||||
| chr19:1628597
|
C | CGGGGGTG others(95): Show |
1 | a0001c0004t0011g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.299-1172_299-1171i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGGTG others(26): Show |
1 | a0001c0003t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299-1172_299-1171i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGGTG others(127): Show |
5 | a0002c0001t0007g0065a0002c0001t0019g0084a0002c0001t0064g0053others(2): Show | 5 | HG00609.hp2 NA18950.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1172_299-1171i others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGGTG others(126): Show |
1 | a0001c0007t0002g0049 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.299-1172_299-1171i others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGGTG others(329): Show |
1 | a0002c0001t0014g0058 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.299-1172_299-1171i others(338): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGTGA others(58): Show |
1 | a0002c0001t0022g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-1172_299-1171i others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGTGA others(93): Show |
1 | a0001c0005t0009g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.299-1172_299-1171i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGTGA others(60): Show |
2 | a0002c0001t0006g0076a0002c0001t0007g0061 | 2 | HG00408.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.299-1172_299-1171i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGTGA others(295): Show |
1 | a0002c0001t0087g0291 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.299-1172_299-1171i others(304): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGTGA others(25): Show |
1 | a0002c0001t0022g0318 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.299-1172_299-1171i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGTGA others(127): Show |
1 | a0002c0001t0016g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.299-1172_299-1171i others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
C | CGGGGTGA others(329): Show |
1 | a0002c0001t0006g0083 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.299-1172_299-1171i others(338): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
CA | C | 42 | a0001c0002t0001g0173a0001c0002t0004g0012a0001c0002t0005g0328others(39): Show | 42 | HG00642.hp2 HG01070.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.299-1172delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628597
|
CAG | C | 40 | a0001c0002t0001g0078a0001c0002t0001g0138a0001c0002t0001g0180others(37): Show | 40 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.299-1173_299-1172d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628597 | ||||||
| chr19:1628598
|
A | AGGGGGTG others(11): Show |
1 | a0001c0007t0002g0127 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-1190_299-1173d others(20): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628598 | ||||||
| chr19:1628598
|
A | AGGGGGTG others(95): Show |
1 | a0001c0004t0011g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-1173_299-1172i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628598 | ||||||
| chr19:1628598
|
A | AGGGGGTG others(60): Show |
1 | a0002c0001t0007g0060 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.299-1173_299-1172i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628598 | ||||||
| chr19:1628598
|
A | AGGGGGTG others(27): Show |
1 | a0002c0001t0007g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.299-1173_299-1172i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628598 | ||||||
| chr19:1628598
|
A | C | 6 | a0001c0003t0001g0255a0001c0004t0011g0137a0002c0001t0006g0076others(3): Show | 6 | HG00408.hp1 HG01074.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1172T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628598 | ||||||
| chr19:1628598
|
A | G | 2 | a0001c0004t0003g0280a0001c0007t0002g0149 | 2 | HG02300.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.299-1172T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628598 | ||||||
| chr19:1628598
|
A | T | 17 | a0001c0005t0009g0029a0001c0007t0002g0049a0002c0001t0006g0067others(14): Show | 17 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-1172T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628598 | ||||||
| chr19:1628599
|
G | C | 12 | a0001c0002t0001g0132a0001c0002t0001g0265a0001c0002t0002g0133others(9): Show | 12 | HG00735.hp2 HG01255.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-1173C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628599
|
G | GGGGATGA others(26): Show |
1 | a0001c0005t0027g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.299-1174_299-1173i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628599
|
G | GGGGATGA others(93): Show |
1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.299-1174_299-1173i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628599
|
G | GGGGATGA others(162): Show |
1 | a0001c0002t0005g0330 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.299-1174_299-1173i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628599
|
G | GGGGGTGA others(26): Show |
2 | a0001c0004t0003g0099a0001c0004t0008g0097 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.299-1174_299-1173i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628599
|
G | GGGGGTGA others(60): Show |
1 | a0001c0003t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.299-1174_299-1173i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628599
|
G | GGGGGTGG others(96): Show |
1 | a0001c0007t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.299-1174_299-1173i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628599
|
G | T | 2 | a0001c0002t0002g0186a0001c0002t0002g0191 | 2 | HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299-1173C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628599 | ||||||
| chr19:1628600
|
G | A | 1 | a0001c0009t0050g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.299-1174C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628600 | ||||||
| chr19:1628603
|
G | A | 34 | a0001c0002t0001g0203a0001c0002t0001g0209a0001c0002t0001g0212others(31): Show | 34 | HG01167.hp1 HG01168.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.299-1177C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628603 | ||||||
| chr19:1628603
|
G | GTGAGGCG others(27): Show |
1 | a0001c0004t0002g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-1178_299-1177i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628603 | ||||||
| chr19:1628605
|
G | A | 4 | a0001c0002t0001g0215a0001c0002t0001g0265a0001c0002t0002g0264others(1): Show | 4 | NA18970.hp2 NA19057.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1179C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628605 | ||||||
| chr19:1628606
|
A | G | 21 | a0001c0002t0005g0328a0001c0003t0001g0255a0001c0004t0001g0110others(18): Show | 21 | HG00408.hp1 HG01074.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.299-1180T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628606 | ||||||
| chr19:1628609
|
C | CGGGAAGG others(167): Show |
1 | a0001c0002t0078g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-1184_299-1183i others(176): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628609 | ||||||
| chr19:1628609
|
C | CGGGAAGG others(397): Show |
1 | a0001c0005t0039g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.299-1184_299-1183i others(406): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628609 | ||||||
| chr19:1628609
|
C | T | 7 | a0001c0004t0021g0312a0001c0004t0102g0344a0001c0005t0009g0021others(4): Show | 7 | HG00408.hp2 HG02258.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-1183G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628609 | ||||||
| chr19:1628610
|
G | C | 1 | a0001c0003t0005g0338 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.299-1184C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628610 | ||||||
| chr19:1628612
|
G | A | 2 | a0004c0014t0079g0305a0017c0026t0002g0112 | 2 | HG00423.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.299-1186C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628612 | ||||||
| chr19:1628615
|
G | A | 9 | a0001c0002t0005g0330a0001c0004t0002g0108a0001c0004t0003g0091others(6): Show | 9 | HG00140.hp2 HG02027.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-1189C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628615 | ||||||
| chr19:1628615
|
G | GGGGACAG others(434): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-1190_299-1189i others(443): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628615 | ||||||
| chr19:1628615
|
G | GGGGACAG others(129): Show |
1 | a0001c0003t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-1190_299-1189i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628615 | ||||||
| chr19:1628623
|
C | T | 6 | a0002c0001t0001g0122a0003c0006t0001g0125a0003c0006t0002g0150others(3): Show | 6 | HG02135.hp2 NA18612.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1197G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628623 | ||||||
| chr19:1628627
|
A | G | 157 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.299-1201T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628627 | ||||||
| chr19:1628631
|
A | G | 1 | a0002c0001t0057g0158 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.299-1205T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628631 | ||||||
| chr19:1628631
|
ACGGGGTG others(398): Show |
A | 2 | a0001c0009t0050g0168a0005c0010t0018g0170 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.299-1610_299-1206d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628631 | ||||||
| chr19:1628632
|
C | CAG | 52 | a0001c0002t0001g0181a0001c0002t0002g0210a0001c0002t0005g0319others(49): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.299-1207_299-1206i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | CAGGGGAT others(97): Show |
2 | a0003c0006t0001g0115a0003c0006t0017g0294 | 2 | NA18964.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.299-1207_299-1206i others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | CAGGGGGT others(65): Show |
1 | a0001c0003t0059g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.299-1207_299-1206i others(74): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | CG | 25 | a0001c0002t0002g0191a0001c0004t0003g0153a0001c0004t0003g0220others(22): Show | 25 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.299-1207dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | CGGGGGTG others(167): Show |
1 | a0001c0004t0021g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.299-1207_299-1206i others(176): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | CGGGGTGA others(745): Show |
1 | a0001c0007t0091g0300 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.299-1207_299-1206i others(754): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | CGGGGTGA others(27): Show |
1 | a0001c0004t0008g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.299-1207_299-1206i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | G | 2 | a0002c0001t0015g0080a0002c0001t0022g0308 | 2 | HG01358.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.299-1206G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
C | T | 4 | a0001c0004t0001g0110a0001c0004t0002g0154a0001c0004t0003g0106others(1): Show | 4 | HG01123.hp2 HG02109.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1206G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
CGGGGTGA others(98): Show |
C | 1 | a0001c0003t0005g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.299-1311_299-1207d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628632
|
CGGGGTGA others(467): Show |
C | 1 | a0001c0004t0003g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.299-1680_299-1207d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628632 | ||||||
| chr19:1628636
|
G | A | 8 | a0001c0002t0002g0210a0001c0003t0059g0187a0001c0003t0076g0045others(5): Show | 8 | HG02165.hp2 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1210C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628636 | ||||||
| chr19:1628636
|
G | GA | 5 | a0001c0004t0001g0110a0001c0004t0002g0154a0001c0004t0003g0106others(2): Show | 5 | HG01123.hp2 HG02109.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1211_299-1210i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628636 | ||||||
| chr19:1628636
|
G | GGTGAGGC others(29): Show |
1 | a0001c0002t0001g0203 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.299-1211_299-1210i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628636 | ||||||
| chr19:1628636
|
G | GTGGGGCG others(28): Show |
1 | a0001c0003t0002g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.299-1211_299-1210i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628636 | ||||||
| chr19:1628638
|
G | A | 1 | a0001c0005t0002g0224 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.299-1212C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628638 | ||||||
| chr19:1628639
|
A | AGGCGGGA others(500): Show |
1 | a0001c0002t0035g0349 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299-1214_299-1213i others(509): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628639 | ||||||
| chr19:1628639
|
A | AGGCGGGA others(162): Show |
1 | a0001c0002t0075g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-1214_299-1213i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628639 | ||||||
| chr19:1628639
|
A | G | 7 | a0001c0004t0001g0110a0001c0004t0002g0154a0001c0004t0003g0106others(4): Show | 7 | HG01123.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-1213T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628639 | ||||||
| chr19:1628642
|
C | T | 20 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0002g0133others(17): Show | 20 | HG00735.hp2 HG01099.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-1216G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628642 | ||||||
| chr19:1628643
|
G | A | 1 | a0001c0007t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.299-1217C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628643 | ||||||
| chr19:1628645
|
G | A | 5 | a0002c0001t0015g0080a0002c0001t0022g0308a0003c0006t0001g0119others(2): Show | 5 | HG01358.hp2 HG02132.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1219C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628645 | ||||||
| chr19:1628648
|
G | A | 1 | a0001c0004t0003g0280 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-1222C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628648 | ||||||
| chr19:1628655
|
G | C | 1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-1229C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628655 | ||||||
| chr19:1628656
|
C | T | 10 | a0001c0007t0002g0127a0001c0025t0010g0266a0003c0006t0001g0125others(7): Show | 10 | HG00323.hp1 HG00544.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-1230G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628656 | ||||||
| chr19:1628660
|
G | A | 17 | a0001c0002t0001g0198a0001c0002t0002g0210a0001c0002t0085g0304others(14): Show | 17 | HG00140.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.299-1234C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628660 | ||||||
| chr19:1628664
|
A | ACGGGGAT others(60): Show |
1 | a0001c0002t0004g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.299-1239_299-1238i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ACGGGGAT others(294): Show |
1 | a0016c0027t0004g0020 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.299-1239_299-1238i others(303): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ACGGGGAT others(59): Show |
1 | a0001c0005t0004g0005 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.299-1239_299-1238i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ACGGGGGT others(331): Show |
1 | a0001c0003t0001g0233 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.299-1239_299-1238i others(340): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ACGGGGGT others(92): Show |
1 | a0002c0001t0088g0292 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.299-1239_299-1238i others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ACGGGGTG others(192): Show |
1 | a0001c0005t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.299-1239_299-1238i others(201): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ACGGGGTG others(158): Show |
1 | a0001c0002t0065g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.299-1239_299-1238i others(167): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ACGGGGTG others(395): Show |
1 | a0002c0001t0019g0056 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.299-1239_299-1238i others(404): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ATGGGGGT others(160): Show |
1 | a0002c0001t0019g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.299-1239_299-1238i others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | ATGGGGGT others(25): Show |
1 | a0002c0001t0095g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.299-1239_299-1238i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
A | G | 2 | a0002c0001t0007g0070a0002c0001t0015g0081 | 2 | HG02004.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.299-1238T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628664
|
AC | A | 6 | a0001c0002t0001g0138a0001c0013t0037g0009a0002c0001t0014g0059others(3): Show | 6 | HG01109.hp2 HG02559.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1239delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628664 | ||||||
| chr19:1628665
|
C | CGGGGGTG others(59): Show |
3 | a0002c0001t0007g0065a0002c0001t0019g0084a0013c0022t0007g0066 | 3 | NA19000.hp1 NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.299-1240_299-1239i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628665 | ||||||
| chr19:1628665
|
CA | C | 18 | a0001c0003t0002g0287a0001c0003t0005g0331a0001c0003t0076g0045others(15): Show | 18 | HG00544.hp1 HG01074.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-1240delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628665 | ||||||
| chr19:1628665
|
CAG | C | 64 | a0001c0002t0001g0111a0001c0002t0001g0173a0001c0002t0001g0180others(61): Show | 64 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.299-1241_299-1240d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628665 | ||||||
| chr19:1628665
|
CAGGGGGT others(30): Show |
C | 2 | a0001c0002t0002g0210a0003c0008t0001g0118 | 2 | HG02165.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.299-1276_299-1240d others(39): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628665 | ||||||
| chr19:1628665
|
CAGGGGGT others(65): Show |
C | 2 | a0001c0004t0011g0102a0002c0001t0100g0342 | 2 | HG03927.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.299-1311_299-1240d others(74): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628665 | ||||||
| chr19:1628666
|
A | AGGGGGTG others(1072): Show |
1 | a0002c0001t0054g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.299-1241_299-1240i others(1081): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628666 | ||||||
| chr19:1628666
|
A | AGGGGGTG others(234): Show |
1 | a0003c0006t0010g0141 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.299-1241_299-1240i others(243): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628666 | ||||||
| chr19:1628666
|
A | AGGGGTGA others(855): Show |
1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-1241_299-1240i others(864): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628666 | ||||||
| chr19:1628666
|
A | C | 3 | a0002c0001t0007g0065a0002c0001t0019g0084a0013c0022t0007g0066 | 3 | NA19000.hp1 NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.299-1240T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628666 | ||||||
| chr19:1628666
|
A | G | 2 | a0001c0004t0003g0106a0002c0001t0029g0159 | 2 | HG00738.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.299-1240T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628666 | ||||||
| chr19:1628666
|
A | T | 6 | a0001c0002t0001g0138a0001c0013t0037g0009a0002c0001t0014g0059others(3): Show | 6 | HG01109.hp2 HG02559.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1240T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628666 | ||||||
| chr19:1628667
|
G | C | 10 | a0001c0002t0004g0012a0001c0002t0065g0176a0001c0003t0001g0233others(7): Show | 10 | HG00609.hp2 HG01346.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-1241C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628667
|
G | GGGGATGA others(94): Show |
1 | a0001c0004t0086g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.299-1242_299-1241i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628667
|
G | GGGGGTGA others(1176): Show |
1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299-1242_299-1241i others(1185): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628667
|
G | GGGGGTGA others(95): Show |
2 | a0001c0002t0041g0004a0001c0002t0046g0039 | 2 | HG01109.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.299-1242_299-1241i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628667
|
G | GGGGGTGA others(674): Show |
1 | a0001c0005t0025g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.299-1242_299-1241i others(683): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628667
|
G | GGGGGTGA others(952): Show |
1 | a0001c0005t0023g0032 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.299-1242_299-1241i others(961): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628667
|
G | GGGGGTGA others(95): Show |
1 | a0002c0001t0007g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.299-1242_299-1241i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628667
|
G | GGGGGTGA others(26): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-1242_299-1241i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628667 | ||||||
| chr19:1628671
|
G | A | 20 | a0001c0002t0001g0078a0001c0002t0001g0215a0001c0002t0001g0265others(17): Show | 20 | HG01261.hp2 HG02004.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-1245C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628671 | ||||||
| chr19:1628671
|
G | GTGAGGCG others(368): Show |
1 | a0001c0002t0036g0348 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-1246_299-1245i others(377): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628671 | ||||||
| chr19:1628673
|
G | A | 4 | a0001c0002t0002g0214a0001c0005t0001g0207a0001c0005t0010g0117others(1): Show | 4 | HG01081.hp1 NA18986.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1247C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628673 | ||||||
| chr19:1628673
|
G | GAGGCGGG others(162): Show |
1 | a0001c0002t0002g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.299-1248_299-1247i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628673 | ||||||
| chr19:1628674
|
A | G | 21 | a0001c0002t0001g0203a0001c0002t0005g0328a0001c0002t0065g0176others(18): Show | 21 | HG01109.hp2 HG01358.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-1248T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628674 | ||||||
| chr19:1628675
|
G | C | 1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-1249C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628675 | ||||||
| chr19:1628675
|
G | T | 3 | a0003c0006t0001g0116a0003c0006t0067g0130a0003c0008t0001g0113 | 3 | HG02723.hp1 HG03704.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.299-1249C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628675 | ||||||
| chr19:1628677
|
C | CGGGAAGG others(95): Show |
1 | a0001c0004t0003g0109 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.299-1252_299-1251i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628677 | ||||||
| chr19:1628677
|
C | CGGGAAGG others(94): Show |
1 | a0001c0005t0009g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.299-1252_299-1251i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628677 | ||||||
| chr19:1628677
|
C | CGGGAAGG others(161): Show |
1 | a0002c0001t0006g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.299-1252_299-1251i others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628677 | ||||||
| chr19:1628677
|
C | CGGGAAGG others(61): Show |
1 | a0002c0001t0006g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.299-1252_299-1251i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628677 | ||||||
| chr19:1628677
|
C | T | 17 | a0001c0002t0001g0203a0001c0002t0005g0330a0001c0003t0001g0096others(14): Show | 17 | HG00741.hp2 HG01257.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-1251G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628677 | ||||||
| chr19:1628678
|
G | A | 1 | a0001c0002t0005g0328 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.299-1252C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628678 | ||||||
| chr19:1628678
|
G | GGGAAGGG others(28): Show |
1 | a0001c0004t0003g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-1253_299-1252i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628678 | ||||||
| chr19:1628680
|
A | G | 280 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(277): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.299-1254T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628680 | ||||||
| chr19:1628683
|
G | A | 1 | a0001c0002t0032g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-1257C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628683 | ||||||
| chr19:1628684
|
G | C | 1 | a0001c0004t0011g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-1258C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628684 | ||||||
| chr19:1628690
|
G | C | 1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-1264C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628690 | ||||||
| chr19:1628690
|
G | GCAGAGCT others(60): Show |
1 | a0001c0003t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-1265_299-1264i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628690 | ||||||
| chr19:1628691
|
C | A | 1 | a0001c0007t0002g0149 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.299-1265G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628691 | ||||||
| chr19:1628691
|
C | T | 13 | a0001c0007t0002g0127a0001c0007t0002g0282a0001c0007t0012g0323others(10): Show | 13 | HG00323.hp1 HG00544.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.299-1265G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628691 | ||||||
| chr19:1628695
|
G | A | 22 | a0001c0002t0001g0174a0001c0002t0001g0215a0001c0002t0001g0265others(19): Show | 22 | HG01175.hp1 HG01192.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.299-1269C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628695 | ||||||
| chr19:1628699
|
A | ACGGGGAT others(1072): Show |
1 | a0001c0005t0009g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.299-1274_299-1273i others(1081): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGGT others(297): Show |
2 | a0002c0001t0016g0052a0002c0001t0016g0269 | 2 | HG00642.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.299-1274_299-1273i others(306): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGGT others(638): Show |
1 | a0001c0005t0038g0025 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.299-1274_299-1273i others(647): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGGT others(462): Show |
1 | a0001c0002t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299-1274_299-1273i others(471): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGGT others(60): Show |
1 | a0001c0004t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299-1274_299-1273i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(58): Show |
1 | a0002c0001t0015g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-1274_299-1273i others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(399): Show |
1 | a0003c0006t0035g0345 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.299-1274_299-1273i others(408): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(59): Show |
4 | a0001c0002t0002g0214a0001c0005t0001g0207a0001c0005t0010g0117others(1): Show | 4 | HG01081.hp1 NA18986.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1274_299-1273i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(158): Show |
1 | a0001c0002t0002g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.299-1274_299-1273i others(167): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(122): Show |
1 | a0002c0001t0007g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.299-1274_299-1273i others(131): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(58): Show |
1 | a0002c0001t0034g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.299-1274_299-1273i others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(398): Show |
1 | a0002c0001t0016g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.299-1274_299-1273i others(407): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(397): Show |
1 | a0002c0001t0014g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.299-1274_299-1273i others(406): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | ACGGGGTG others(564): Show |
1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.299-1274_299-1273i others(573): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
A | G | 15 | a0001c0005t0009g0029a0001c0007t0001g0217a0001c0007t0002g0049others(12): Show | 15 | HG00673.hp1 HG00738.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-1273T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628699
|
AC | A | 5 | a0001c0004t0001g0110a0001c0004t0002g0154a0002c0001t0006g0068others(2): Show | 5 | HG02109.hp1 HG02273.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1274delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628699 | ||||||
| chr19:1628700
|
C | CGGGGGTG others(197): Show |
1 | a0001c0007t0020g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.299-1275_299-1274i others(206): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628700 | ||||||
| chr19:1628700
|
C | CGGGGTGA others(60): Show |
1 | a0003c0006t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-1275_299-1274i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628700 | ||||||
| chr19:1628700
|
CA | C | 31 | a0001c0002t0001g0180a0001c0002t0002g0188a0001c0002t0075g0185others(28): Show | 31 | HG00323.hp1 HG00673.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.299-1275delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628700 | ||||||
| chr19:1628700
|
CAG | C | 54 | a0001c0002t0001g0213a0001c0002t0001g0215a0001c0002t0001g0218others(51): Show | 54 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.299-1276_299-1275d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628700 | ||||||
| chr19:1628700
|
CAGGGGAT others(65): Show |
C | 1 | a0001c0007t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.299-1346_299-1275d others(74): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628700 | ||||||
| chr19:1628700
|
CAGGGGAT others(130): Show |
C | 2 | a0001c0002t0001g0271a0001c0002t0002g0270 | 2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.299-1411_299-1275d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628700 | ||||||
| chr19:1628701
|
A | AGGGGGTG others(375): Show |
1 | a0001c0007t0012g0323 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.299-1276_299-1275i others(384): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628701 | ||||||
| chr19:1628701
|
A | AGGGGTGA others(129): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-1276_299-1275i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628701 | ||||||
| chr19:1628701
|
A | C | 2 | a0001c0007t0020g0289a0003c0006t0001g0092 | 2 | HG01891.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.299-1275T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628701 | ||||||
| chr19:1628701
|
A | G | 1 | a0002c0001t0006g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.299-1275T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628701 | ||||||
| chr19:1628701
|
A | T | 5 | a0001c0004t0001g0110a0001c0004t0002g0154a0002c0001t0006g0068others(2): Show | 5 | HG02109.hp1 HG02273.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1275T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628701 | ||||||
| chr19:1628702
|
G | C | 18 | a0001c0002t0002g0048a0001c0002t0002g0214a0001c0002t0002g0267others(15): Show | 18 | HG00597.hp2 HG00642.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-1276C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(60): Show |
10 | a0001c0005t0009g0029a0001c0007t0002g0049a0002c0001t0006g0063others(7): Show | 10 | HG00673.hp1 HG01943.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-1277_299-1276i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(26): Show |
1 | a0001c0002t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.299-1277_299-1276i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(330): Show |
1 | a0001c0005t0009g0022 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.299-1277_299-1276i others(339): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(164): Show |
2 | a0001c0005t0004g0011a0001c0005t0004g0027 | 2 | HG04115.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.299-1277_299-1276i others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(95): Show |
1 | a0001c0005t0004g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.299-1277_299-1276i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(93): Show |
1 | a0001c0005t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.299-1277_299-1276i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(94): Show |
1 | a0001c0007t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-1277_299-1276i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGGTGA others(807): Show |
1 | a0001c0005t0023g0015 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.299-1277_299-1276i others(816): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628702
|
G | GGGGTGAG others(93): Show |
1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.299-1277_299-1276i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628702 | ||||||
| chr19:1628703
|
G | A | 1 | a0006c0012t0020g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.299-1277C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628703 | ||||||
| chr19:1628706
|
A | ATGAGGCG others(28): Show |
1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.299-1281_299-1280i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628706
|
A | ATGAGGCG others(26): Show |
3 | a0001c0002t0001g0212a0008c0032t0061g0211a0011c0031t0048g0043 | 3 | NA19012.hp1 NA19055.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.299-1281_299-1280i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628706
|
A | ATGAGGCG others(1011): Show |
1 | a0001c0004t0002g0257 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.299-1281_299-1280i others(1020): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628706
|
A | ATGAGGCG others(1717): Show |
1 | a0001c0003t0005g0340 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.299-1281_299-1280i others(1726): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628706
|
A | ATGAGGCG others(630): Show |
1 | a0001c0002t0001g0209 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.299-1281_299-1280i others(639): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628706
|
A | ATGAGGCG others(94): Show |
1 | a0001c0002t0002g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-1281_299-1280i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628706
|
A | ATGAGGCG others(62): Show |
1 | a0001c0007t0002g0127 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-1281_299-1280i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628706
|
A | G | 222 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0138others(219): Show | 222 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.299-1280T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628706 | ||||||
| chr19:1628708
|
G | A | 1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299-1282C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628708 | ||||||
| chr19:1628709
|
A | AGGCGGGA others(61): Show |
1 | a0001c0004t0011g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-1284_299-1283i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628709 | ||||||
| chr19:1628709
|
A | G | 13 | a0001c0002t0001g0180a0001c0003t0002g0095a0001c0003t0076g0045others(10): Show | 13 | HG00741.hp1 HG02109.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.299-1283T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628709 | ||||||
| chr19:1628710
|
G | C | 2 | a0004c0033t0036g0350a0005c0010t0018g0169 | 2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299-1284C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628710 | ||||||
| chr19:1628710
|
G | GGCGGGAA others(162): Show |
1 | a0001c0004t0008g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.299-1285_299-1284i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628710 | ||||||
| chr19:1628710
|
G | T | 3 | a0001c0003t0002g0094a0001c0003t0008g0098a0001c0007t0002g0282 | 3 | HG00280.hp2 HG02602.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.299-1284C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628710 | ||||||
| chr19:1628712
|
C | CGGAAAGG others(93): Show |
1 | a0002c0001t0006g0083 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.299-1287_299-1286i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628712
|
C | CGGGAAAG others(91): Show |
2 | a0001c0004t0003g0105a0001c0004t0011g0145 | 2 | HG00735.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.299-1287_299-1286i others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628712
|
C | CGGGAAAG others(294): Show |
1 | a0001c0004t0003g0106 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.299-1287_299-1286i others(303): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628712
|
C | CGGGAAAG others(62): Show |
1 | a0001c0002t0032g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-1287_299-1286i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628712
|
C | CGGGAAGG others(97): Show |
1 | a0001c0003t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.299-1287_299-1286i others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628712
|
C | CGGGAAGG others(264): Show |
1 | a0001c0004t0003g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299-1287_299-1286i others(273): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628712
|
C | T | 18 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0003t0001g0096others(15): Show | 18 | HG00408.hp1 HG00741.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.299-1286G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628712
|
C | TGGGAAGG others(60): Show |
1 | a0002c0001t0022g0318 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.299-1286_299-1285i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628712 | ||||||
| chr19:1628713
|
G | A | 2 | a0001c0007t0074g0090a0001c0007t0096g0311 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.299-1287C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628713 | ||||||
| chr19:1628713
|
G | GGGAAGGG others(2004): Show |
1 | a0001c0004t0003g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-1288_299-1287i others(2013): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628713 | ||||||
| chr19:1628715
|
G | A | 5 | a0001c0005t0001g0204a0001c0007t0001g0232a0002c0001t0014g0058others(2): Show | 5 | HG00738.hp1 HG02698.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1289C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628715 | ||||||
| chr19:1628715
|
G | GAAGGGGA others(535): Show |
1 | a0001c0003t0005g0336 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.299-1290_299-1289i others(544): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628715 | ||||||
| chr19:1628715
|
G | GAAGGGGA others(27): Show |
2 | a0001c0007t0002g0278a0001c0007t0012g0335 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.299-1290_299-1289i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628715 | ||||||
| chr19:1628718
|
G | A | 6 | a0001c0002t0002g0133a0001c0003t0002g0001a0002c0001t0015g0088others(3): Show | 7 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-1292C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628718 | ||||||
| chr19:1628725
|
G | C | 2 | a0001c0004t0003g0099a0001c0004t0008g0097 | 2 | HG00639.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.299-1299C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628725 | ||||||
| chr19:1628726
|
C | CAGAGCTC others(300): Show |
1 | a0017c0026t0002g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.299-1301_299-1300i others(309): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628726 | ||||||
| chr19:1628726
|
C | CAGAGCTC others(27): Show |
1 | a0001c0005t0009g0013 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.299-1301_299-1300i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628726 | ||||||
| chr19:1628726
|
C | T | 9 | a0001c0007t0002g0127a0001c0007t0012g0323a0001c0025t0010g0266others(6): Show | 9 | HG00323.hp1 HG00558.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-1300G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628726 | ||||||
| chr19:1628730
|
G | A | 22 | a0001c0002t0002g0133a0001c0002t0002g0143a0001c0002t0002g0272others(19): Show | 22 | HG00438.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.299-1304C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628730 | ||||||
| chr19:1628734
|
A | ACGGGGGT others(527): Show |
1 | a0001c0002t0001g0216 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.299-1309_299-1308i others(536): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGGT others(58): Show |
1 | a0001c0003t0001g0201 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.299-1309_299-1308i others(67): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGGT others(25): Show |
1 | a0002c0001t0015g0088 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.299-1309_299-1308i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGGT others(356): Show |
1 | a0001c0002t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299-1309_299-1308i others(365): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(57): Show |
1 | a0001c0002t0083g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.299-1309_299-1308i others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(24): Show |
2 | a0001c0005t0026g0037a0012c0030t0002g0163 | 2 | HG01934.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.299-1309_299-1308i others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(772): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-1309_299-1308i others(781): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(127): Show |
3 | a0001c0003t0005g0332a0001c0003t0012g0333a0001c0003t0033g0324 | 3 | HG00140.hp1 HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.299-1309_299-1308i others(136): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(157): Show |
2 | a0001c0002t0002g0222a0001c0002t0005g0322 | 2 | NA19064.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.299-1309_299-1308i others(166): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(259): Show |
1 | a0001c0002t0001g0213 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.299-1309_299-1308i others(268): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(123): Show |
1 | a0001c0002t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.299-1309_299-1308i others(132): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ACGGGGTG others(364): Show |
1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-1309_299-1308i others(373): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ATGGGGAT others(25): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-1309_299-1308i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | ATGGGGGT others(92): Show |
4 | a0002c0001t0006g0076a0002c0001t0007g0061a0002c0001t0073g0079others(1): Show | 4 | HG00408.hp1 NA18947.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1309_299-1308i others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628734
|
A | G | 3 | a0002c0001t0019g0284a0002c0001t0054g0157a0002c0001t0069g0082 | 3 | HG02056.hp1 NA18969.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.299-1308T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628734 | ||||||
| chr19:1628735
|
C | CGGGGTGA others(91): Show |
1 | a0001c0029t0002g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.299-1310_299-1309i others(100): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628735 | ||||||
| chr19:1628735
|
CA | C | 24 | a0001c0002t0001g0111a0001c0002t0058g0283a0001c0003t0001g0200others(21): Show | 24 | HG00423.hp1 HG00673.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.299-1310delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628735 | ||||||
| chr19:1628735
|
CAG | C | 52 | a0001c0002t0001g0132a0001c0002t0001g0174a0001c0002t0001g0215others(49): Show | 52 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.299-1311_299-1310d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628735 | ||||||
| chr19:1628736
|
A | AGGGGATG others(129): Show |
1 | a0001c0004t0003g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-1311_299-1310i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | AGGGGGTG others(373): Show |
1 | a0001c0003t0005g0338 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.299-1311_299-1310i others(382): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | AGGGGGTG others(298): Show |
1 | a0001c0004t0003g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.299-1311_299-1310i others(307): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | AGGGGGTG others(717): Show |
1 | a0001c0002t0013g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.299-1311_299-1310i others(726): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | AGGGGGTG others(95): Show |
1 | a0001c0003t0002g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.299-1311_299-1310i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | AGGGGTGA others(717): Show |
1 | a0020c0034t0010g0146 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.299-1311_299-1310i others(726): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | C | 1 | a0001c0029t0002g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.299-1310T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | G | 23 | a0001c0002t0001g0198a0001c0004t0001g0110a0001c0004t0002g0154others(20): Show | 23 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.299-1310T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
A | TGGGGGTG others(61): Show |
1 | a0002c0001t0006g0075 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.299-1310_299-1309i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628736
|
AG | A | 6 | a0001c0004t0003g0153a0001c0004t0011g0135a0001c0004t0011g0136others(3): Show | 6 | HG00741.hp2 HG01257.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1311delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628736 | ||||||
| chr19:1628737
|
G | C | 20 | a0001c0002t0001g0078a0001c0002t0001g0180a0001c0002t0001g0213others(17): Show | 20 | HG00140.hp1 HG00408.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-1311C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGATGA others(233): Show |
1 | a0001c0003t0002g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(242): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGATGA others(769): Show |
1 | a0002c0001t0029g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(778): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(94): Show |
1 | a0001c0007t0091g0300 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(26): Show |
1 | a0002c0001t0006g0072 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.299-1312_299-1311i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(26): Show |
1 | a0001c0003t0005g0325 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.299-1344_299-1312d others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(27): Show |
1 | a0003c0006t0002g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.299-1345_299-1312d others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(199): Show |
1 | a0007c0016t0002g0260 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(208): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(234): Show |
1 | a0001c0007t0090g0306 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(243): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(715): Show |
1 | a0001c0004t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(724): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(680): Show |
1 | a0001c0004t0003g0286 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(689): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(300): Show |
1 | a0001c0003t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(309): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(232): Show |
1 | a0001c0003t0002g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.299-1312_299-1311i others(241): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(129): Show |
5 | a0001c0003t0001g0236a0001c0003t0089g0301a0001c0004t0003g0246others(2): Show | 5 | HG01243.hp1 HG01261.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1312_299-1311i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(230): Show |
1 | a0001c0003t0010g0244 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.299-1312_299-1311i others(239): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628737
|
G | GGGGGTGA others(1964): Show |
1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-1312_299-1311i others(1973): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628737 | ||||||
| chr19:1628738
|
G | A | 1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.299-1312C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628738 | ||||||
| chr19:1628741
|
G | A | 28 | a0001c0002t0001g0218a0001c0002t0002g0188a0001c0002t0004g0012others(25): Show | 28 | HG00544.hp2 HG00673.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.299-1315C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628741 | ||||||
| chr19:1628744
|
A | AGGCGGAA others(27): Show |
1 | a0002c0001t0069g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.299-1319_299-1318i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628744 | ||||||
| chr19:1628744
|
A | AGGCGGGA others(94): Show |
1 | a0001c0004t0002g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.299-1319_299-1318i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628744 | ||||||
| chr19:1628744
|
A | AGGCGGGA others(330): Show |
1 | a0001c0003t0005g0325 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.299-1319_299-1318i others(339): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628744 | ||||||
| chr19:1628744
|
A | ATGCGGGA others(302): Show |
1 | a0001c0003t0005g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-1319_299-1318i others(311): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628744 | ||||||
| chr19:1628744
|
A | G | 14 | a0001c0002t0002g0133a0001c0002t0013g0197a0001c0003t0002g0095others(11): Show | 14 | HG00408.hp2 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-1318T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628744 | ||||||
| chr19:1628745
|
G | A | 2 | a0001c0002t0013g0197a0003c0008t0001g0118 | 2 | HG02735.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.299-1319C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628745 | ||||||
| chr19:1628745
|
G | T | 3 | a0001c0004t0003g0099a0001c0007t0002g0282a0003c0006t0035g0345 | 3 | HG00597.hp2 HG00642.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.299-1319C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628745 | ||||||
| chr19:1628747
|
C | CGGGAAGG others(369): Show |
1 | a0001c0004t0008g0097 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.299-1322_299-1321i others(378): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628747 | ||||||
| chr19:1628747
|
C | CGGGAAGG others(62): Show |
1 | a0001c0003t0076g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-1322_299-1321i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628747 | ||||||
| chr19:1628747
|
C | CGGGAAGG others(26): Show |
1 | a0001c0004t0008g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.299-1322_299-1321i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628747 | ||||||
| chr19:1628747
|
C | CGGGAAGG others(27): Show |
1 | a0001c0007t0003g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-1322_299-1321i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628747 | ||||||
| chr19:1628747
|
C | T | 10 | a0001c0004t0011g0102a0001c0004t0011g0137a0001c0004t0028g0101others(7): Show | 10 | HG00609.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-1321G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628747 | ||||||
| chr19:1628748
|
G | A | 1 | a0001c0003t0005g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-1322C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628748 | ||||||
| chr19:1628749
|
G | T | 1 | a0003c0008t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299-1323C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628749 | ||||||
| chr19:1628750
|
G | A | 2 | a0002c0001t0019g0284a0002c0001t0054g0157 | 2 | HG02056.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.299-1324C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628750 | ||||||
| chr19:1628753
|
G | A | 5 | a0001c0002t0005g0330a0001c0003t0002g0094a0001c0003t0002g0229others(2): Show | 5 | HG00280.hp2 HG02145.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1327C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628753 | ||||||
| chr19:1628761
|
C | CAGAGCTC others(97): Show |
1 | a0003c0008t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-1336_299-1335i others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628761 | ||||||
| chr19:1628761
|
C | T | 9 | a0001c0007t0002g0282a0001c0025t0010g0266a0003c0006t0001g0116others(6): Show | 9 | HG02895.hp2 NA18747.hp2 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-1335G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628761 | ||||||
| chr19:1628765
|
G | A | 14 | a0001c0002t0001g0181a0001c0002t0035g0349a0001c0003t0005g0336others(11): Show | 14 | HG01069.hp1 HG01071.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-1339C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628765 | ||||||
| chr19:1628765
|
G | GCTCACGG others(164): Show |
1 | a0001c0004t0008g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.299-1340_299-1339i others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628765 | ||||||
| chr19:1628769
|
A | ACGGGGGT others(60): Show |
1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-1344_299-1343i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628769 | ||||||
| chr19:1628769
|
A | ACGGGGTG others(162): Show |
1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-1344_299-1343i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628769 | ||||||
| chr19:1628769
|
A | ACGGGGTG others(57): Show |
1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.299-1344_299-1343i others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628769 | ||||||
| chr19:1628769
|
A | ACGGGGTG others(459): Show |
1 | a0001c0003t0055g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.299-1344_299-1343i others(468): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628769 | ||||||
| chr19:1628769
|
A | ACGGGGTG others(126): Show |
1 | a0001c0004t0003g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.299-1344_299-1343i others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628769 | ||||||
| chr19:1628769
|
A | G | 4 | a0002c0001t0006g0075a0002c0001t0022g0318a0002c0001t0034g0309others(1): Show | 4 | HG00621.hp1 NA18963.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1343T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628769 | ||||||
| chr19:1628769
|
AC | A | 10 | a0001c0003t0001g0261a0001c0003t0005g0336a0001c0004t0003g0153others(7): Show | 10 | HG00609.hp1 HG00741.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-1344delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628769 | ||||||
| chr19:1628770
|
C | CGGGGTGA others(160): Show |
1 | a0002c0001t0014g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.299-1345_299-1344i others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628770 | ||||||
| chr19:1628770
|
CA | C | 69 | a0001c0002t0001g0181a0001c0002t0002g0186a0001c0002t0002g0219others(66): Show | 69 | HG00099.hp2 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.299-1345delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628770 | ||||||
| chr19:1628770
|
CAG | C | 29 | a0001c0002t0001g0132a0001c0002t0001g0209a0001c0002t0001g0218others(26): Show | 29 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.299-1346_299-1345d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628770 | ||||||
| chr19:1628771
|
A | AGGGGGTG others(162): Show |
1 | a0002c0001t0084g0290 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.299-1346_299-1345i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628771 | ||||||
| chr19:1628771
|
A | G | 2 | a0002c0001t0006g0089a0002c0001t0095g0317 | 2 | HG02523.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.299-1345T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628771 | ||||||
| chr19:1628771
|
A | T | 11 | a0001c0003t0001g0261a0001c0003t0005g0336a0001c0004t0003g0153others(8): Show | 11 | HG00609.hp1 HG00741.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.299-1345T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628771 | ||||||
| chr19:1628772
|
G | C | 4 | a0001c0002t0001g0111a0001c0003t0055g0235a0001c0004t0003g0044others(1): Show | 4 | HG02129.hp1 HG02559.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1346C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628772 | ||||||
| chr19:1628772
|
G | GGGGGTGA others(129): Show |
1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-1347_299-1346i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628772 | ||||||
| chr19:1628772
|
G | GGGGGTGA others(261): Show |
1 | a0018c0018t0001g0164 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-1347_299-1346i others(270): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628772 | ||||||
| chr19:1628772
|
G | GGGGGTGA others(337): Show |
1 | a0001c0005t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.299-1347_299-1346i others(346): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628772 | ||||||
| chr19:1628772
|
G | T | 1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-1346C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628772 | ||||||
| chr19:1628772
|
GGGGATGA others(26): Show |
G | 2 | a0001c0005t0013g0194a0001c0005t0013g0195 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.299-1379_299-1347d others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628772 | ||||||
| chr19:1628772
|
GGGGATGA others(59): Show |
G | 1 | a0001c0004t0066g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.299-1412_299-1347d others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628772 | ||||||
| chr19:1628773
|
G | A | 2 | a0001c0007t0002g0282a0006c0012t0020g0262 | 2 | HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.299-1347C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628773 | ||||||
| chr19:1628775
|
GA | G | 4 | a0001c0004t0011g0137a0003c0006t0001g0119a0003c0006t0017g0298others(1): Show | 4 | HG01074.hp1 HG03710.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1350delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628775 | ||||||
| chr19:1628776
|
A | ATGAGGCG others(1636): Show |
1 | a0004c0014t0013g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.299-1351_299-1350i others(1645): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628776 | ||||||
| chr19:1628776
|
A | ATGAGGCG others(27): Show |
1 | a0001c0005t0044g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.299-1351_299-1350i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628776 | ||||||
| chr19:1628776
|
A | G | 225 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0174others(222): Show | 226 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.299-1350T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628776 | ||||||
| chr19:1628776
|
ATGAGGCG others(92): Show |
A | 1 | a0001c0003t0077g0241 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.299-1449_299-1351d others(101): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628776 | ||||||
| chr19:1628779
|
A | AGGTGGGA others(26): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-1354_299-1353i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628779 | ||||||
| chr19:1628779
|
A | G | 41 | a0001c0002t0002g0048a0001c0002t0005g0319a0001c0003t0002g0287others(38): Show | 41 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.299-1353T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628779 | ||||||
| chr19:1628780
|
G | T | 1 | a0003c0006t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.299-1354C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628780 | ||||||
| chr19:1628782
|
C | T | 12 | a0001c0002t0005g0319a0001c0004t0003g0109a0001c0004t0008g0097others(9): Show | 12 | HG00408.hp2 HG00639.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-1356G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628782 | ||||||
| chr19:1628783
|
G | A | 3 | a0003c0008t0082g0299a0003c0008t0101g0346a0006c0012t0020g0263 | 3 | HG02486.hp2 HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.299-1357C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628783 | ||||||
| chr19:1628785
|
G | A | 3 | a0001c0003t0009g0007a0002c0001t0034g0309a0003c0006t0002g0120 | 3 | HG01256.hp2 NA19070.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.299-1359C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628785 | ||||||
| chr19:1628788
|
G | A | 12 | a0001c0002t0032g0161a0001c0003t0002g0094a0001c0004t0001g0110others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-1362C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628788 | ||||||
| chr19:1628796
|
C | A | 1 | a0003c0008t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299-1370G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628796 | ||||||
| chr19:1628796
|
C | T | 5 | a0002c0001t0001g0122a0003c0006t0001g0142a0003c0006t0002g0114others(2): Show | 5 | HG02027.hp2 NA18747.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1370G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628796 | ||||||
| chr19:1628800
|
A | ACTCACAG others(1364): Show |
1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-1375_299-1374i others(1373): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628800 | ||||||
| chr19:1628800
|
A | ACTCACGG others(193): Show |
1 | a0001c0003t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.299-1375_299-1374i others(202): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628800 | ||||||
| chr19:1628800
|
A | ACTCACGG others(1439): Show |
1 | a0012c0030t0002g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.299-1375_299-1374i others(1448): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628800 | ||||||
| chr19:1628800
|
A | G | 164 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(161): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.299-1374T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628800 | ||||||
| chr19:1628804
|
A | ATGGGGAT others(160): Show |
1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-1379_299-1378i others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628804 | ||||||
| chr19:1628805
|
C | CAG | 42 | a0001c0002t0001g0212a0001c0002t0001g0218a0001c0002t0002g0048others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.299-1380_299-1379i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CAGGGGAT others(881): Show |
1 | a0001c0002t0078g0189 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(890): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CAGGGGGT others(575): Show |
1 | a0019c0017t0001g0221 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.299-1380_299-1379i others(584): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CAGGGGTG others(62): Show |
1 | a0003c0006t0017g0294 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CAGGGGTG others(97): Show |
1 | a0003c0006t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CG | 36 | a0001c0002t0001g0173a0001c0002t0001g0181a0001c0002t0002g0272others(33): Show | 37 | HG00558.hp2 HG00609.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.299-1380dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(62): Show |
1 | a0001c0005t0009g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.299-1380_299-1379i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(129): Show |
1 | a0001c0005t0009g0018 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(97): Show |
1 | a0001c0003t0002g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.299-1380_299-1379i others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(196): Show |
1 | a0001c0002t0002g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.299-1380_299-1379i others(205): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(29): Show |
1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(266): Show |
1 | a0001c0004t0008g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(275): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(196): Show |
1 | a0001c0004t0003g0249 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.299-1380_299-1379i others(205): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(234): Show |
1 | a0001c0004t0021g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(243): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGGTG others(263): Show |
1 | a0002c0001t0006g0083 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.299-1380_299-1379i others(272): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | CGGGGTGA others(61): Show |
1 | a0001c0005t0027g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.299-1380_299-1379i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | G | 1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-1379G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628805
|
C | T | 4 | a0001c0004t0011g0137a0001c0004t0062g0046a0001c0007t0003g0107others(1): Show | 4 | HG01074.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1379G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628805 | ||||||
| chr19:1628809
|
G | A | 1 | a0001c0002t0036g0348 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-1383C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628809 | ||||||
| chr19:1628809
|
G | GA | 5 | a0001c0002t0001g0111a0001c0004t0011g0137a0001c0007t0002g0149others(2): Show | 5 | HG01074.hp1 HG02300.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1384_299-1383i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628809 | ||||||
| chr19:1628809
|
G | GGTGAGGC others(131): Show |
1 | a0001c0002t0001g0203 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.299-1384_299-1383i others(140): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628809 | ||||||
| chr19:1628809
|
G | GGTGGGGC others(29): Show |
1 | a0002c0001t0064g0053 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.299-1384_299-1383i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628809 | ||||||
| chr19:1628809
|
G | GGTGGGGC others(97): Show |
1 | a0001c0003t0001g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.299-1384_299-1383i others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628809 | ||||||
| chr19:1628809
|
G | GTGAGGCG others(96): Show |
1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-1384_299-1383i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628809 | ||||||
| chr19:1628812
|
A | G | 20 | a0001c0002t0001g0181a0001c0004t0003g0109a0001c0004t0003g0153others(17): Show | 20 | HG00609.hp2 HG00741.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-1386T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628812 | ||||||
| chr19:1628813
|
G | A | 2 | a0001c0004t0011g0102a0001c0004t0028g0101 | 2 | NA18944.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.299-1387C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628813 | ||||||
| chr19:1628813
|
G | T | 1 | a0014c0020t0034g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.299-1387C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628813 | ||||||
| chr19:1628815
|
C | T | 15 | a0001c0002t0002g0133a0001c0003t0002g0095a0001c0004t0011g0134others(12): Show | 15 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-1389G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628815 | ||||||
| chr19:1628816
|
G | A | 2 | a0001c0004t0021g0321a0001c0007t0001g0238 | 2 | HG02735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.299-1390C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628816 | ||||||
| chr19:1628818
|
G | A | 3 | a0001c0003t0001g0234a0003c0006t0001g0119a0003c0006t0080g0296 | 3 | HG00323.hp2 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.299-1392C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628818 | ||||||
| chr19:1628821
|
G | A | 2 | a0001c0003t0001g0227a0003c0006t0001g0092 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.299-1395C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628821 | ||||||
| chr19:1628829
|
C | A | 4 | a0001c0002t0001g0180a0001c0002t0058g0283a0001c0007t0002g0149others(1): Show | 4 | HG02300.hp1 HG02451.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1403G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628829 | ||||||
| chr19:1628829
|
C | T | 7 | a0001c0005t0023g0015a0001c0005t0038g0025a0002c0001t0054g0157others(4): Show | 7 | HG02027.hp2 HG03834.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-1403G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628829 | ||||||
| chr19:1628833
|
G | A | 16 | a0001c0002t0035g0349a0001c0003t0001g0096a0001c0003t0001g0201others(13): Show | 16 | HG00609.hp1 HG00609.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-1407C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628833
|
G | GCTCACAG others(28): Show |
1 | a0001c0002t0002g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-1408_299-1407i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628833
|
G | GCTCACAG others(738): Show |
1 | a0002c0001t0007g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.299-1408_299-1407i others(747): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628833
|
G | GCTCACAG others(63): Show |
1 | a0002c0001t0014g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.299-1408_299-1407i others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628833
|
G | GCTCACGG others(27): Show |
1 | a0002c0001t0006g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.299-1408_299-1407i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628833
|
G | GCTCACGG others(265): Show |
1 | a0002c0001t0053g0057 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.299-1408_299-1407i others(274): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628833
|
G | GCTCACGG others(61): Show |
1 | a0001c0003t0005g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.299-1408_299-1407i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628833
|
G | GCTCACGG others(129): Show |
1 | a0001c0007t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.299-1408_299-1407i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628833 | ||||||
| chr19:1628837
|
ACGGGGTG others(57): Show |
A | 1 | a0001c0013t0042g0033 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.299-1475_299-1412d others(66): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628837 | ||||||
| chr19:1628838
|
C | CAG | 87 | a0001c0002t0001g0078a0001c0002t0001g0178a0001c0002t0002g0133others(84): Show | 87 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.299-1413_299-1412i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGAT others(302): Show |
1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(311): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGAT others(782): Show |
1 | a0001c0002t0002g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(791): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(63): Show |
1 | a0001c0002t0075g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(30): Show |
1 | a0001c0003t0005g0340 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(39): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(749): Show |
1 | a0001c0002t0002g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(758): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(29): Show |
20 | a0001c0002t0001g0213a0001c0002t0001g0215a0001c0002t0001g0265others(17): Show | 20 | HG01081.hp1 HG01109.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-1413_299-1412i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(64): Show |
1 | a0001c0002t0001g0132 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(73): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(129): Show |
1 | a0002c0001t0022g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(298): Show |
1 | a0002c0001t0007g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(307): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(64): Show |
1 | a0002c0001t0007g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(73): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(169): Show |
1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(178): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CAGGGGGT others(547): Show |
1 | a0001c0003t0059g0187 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(556): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CG | 53 | a0001c0002t0001g0173a0001c0002t0001g0181a0001c0002t0001g0203others(50): Show | 53 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.299-1413dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGGTG others(29): Show |
1 | a0001c0003t0002g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGGTG others(130): Show |
1 | a0001c0004t0011g0134 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGGTG others(98): Show |
1 | a0001c0019t0026g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(107): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(130): Show |
2 | a0001c0002t0002g0222a0001c0002t0005g0322 | 2 | NA19064.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.299-1413_299-1412i others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(1016): Show |
1 | a0001c0003t0009g0007 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(1025): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(27): Show |
1 | a0001c0002t0001g0216 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.299-1446_299-1413d others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(605): Show |
1 | a0001c0005t0009g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(614): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(404): Show |
1 | a0001c0005t0023g0032 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(413): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(438): Show |
2 | a0001c0005t0004g0005a0001c0005t0004g0027 | 2 | HG04115.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.299-1413_299-1412i others(447): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(1328): Show |
1 | a0001c0005t0004g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(1337): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(438): Show |
1 | a0001c0005t0004g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(447): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGA others(664): Show |
1 | a0001c0002t0083g0307 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.299-1413_299-1412i others(673): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | CGGGGTGG others(28): Show |
1 | a0005c0010t0018g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.299-1413_299-1412i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | G | 4 | a0001c0002t0001g0271a0001c0002t0002g0270a0001c0005t0052g0205others(1): Show | 4 | HG03017.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1412G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
C | T | 3 | a0001c0004t0011g0102a0001c0004t0028g0101a0003c0011t0063g0093 | 3 | HG02486.hp1 NA18944.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.299-1412G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628838
|
CGGGGTGA others(127): Show |
C | 1 | a0001c0002t0013g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.299-1546_299-1413d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628838 | ||||||
| chr19:1628842
|
G | A | 6 | a0001c0002t0027g0196a0001c0003t0001g0200a0001c0004t0021g0321others(3): Show | 6 | HG01993.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-1416C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628842 | ||||||
| chr19:1628842
|
G | GA | 9 | a0001c0004t0011g0102a0001c0004t0028g0101a0003c0006t0001g0125others(6): Show | 9 | HG00558.hp2 HG02056.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-1417_299-1416i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628842 | ||||||
| chr19:1628842
|
G | GGTGGGGT others(371): Show |
1 | a0006c0012t0020g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.299-1417_299-1416i others(380): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628842 | ||||||
| chr19:1628842
|
G | GTGAGGCG others(61): Show |
1 | a0001c0005t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.299-1417_299-1416i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628842 | ||||||
| chr19:1628845
|
A | AGGTGGGA others(96): Show |
1 | a0002c0001t0015g0088 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.299-1420_299-1419i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628845 | ||||||
| chr19:1628845
|
A | AGGTGGGA others(740): Show |
1 | a0002c0001t0029g0156 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.299-1420_299-1419i others(749): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628845 | ||||||
| chr19:1628845
|
A | G | 30 | a0001c0002t0001g0174a0001c0002t0093g0341a0001c0003t0076g0045others(27): Show | 30 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.299-1419T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628845 | ||||||
| chr19:1628846
|
G | A | 1 | a0003c0008t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299-1420C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628846 | ||||||
| chr19:1628846
|
G | C | 1 | a0005c0010t0018g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.299-1420C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628846 | ||||||
| chr19:1628846
|
G | T | 4 | a0001c0003t0002g0094a0003c0006t0017g0298a0003c0006t0031g0129others(1): Show | 4 | HG00597.hp2 HG02602.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1420C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628846 | ||||||
| chr19:1628848
|
C | T | 20 | a0001c0002t0001g0138a0001c0002t0032g0161a0001c0002t0083g0307others(17): Show | 20 | HG00140.hp2 HG00735.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-1422G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628848 | ||||||
| chr19:1628849
|
G | A | 3 | a0001c0003t0076g0045a0002c0001t0006g0075a0002c0001t0022g0318 | 3 | HG00621.hp1 HG02970.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.299-1423C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628849 | ||||||
| chr19:1628850
|
G | T | 1 | a0003c0008t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299-1424C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628850 | ||||||
| chr19:1628854
|
G | A | 2 | a0003c0006t0017g0294a0003c0006t0067g0130 | 2 | HG02723.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.299-1428C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628854 | ||||||
| chr19:1628862
|
C | A | 6 | a0003c0006t0001g0125a0003c0006t0002g0077a0003c0006t0002g0123others(3): Show | 6 | HG00558.hp2 HG02056.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1436G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628862 | ||||||
| chr19:1628862
|
C | T | 9 | a0001c0003t0059g0187a0001c0007t0002g0127a0001c0007t0012g0323others(6): Show | 9 | HG00544.hp2 HG02071.hp1 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-1436G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628862 | ||||||
| chr19:1628866
|
G | A | 25 | a0001c0002t0001g0198a0001c0002t0002g0219a0001c0002t0005g0330others(22): Show | 25 | HG00544.hp1 HG00741.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.299-1440C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628866 | ||||||
| chr19:1628866
|
GCTCACGG others(26): Show |
G | 2 | a0001c0002t0002g0272a0001c0003t0002g0001 | 3 | HG01070.hp1 HG01071.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.299-1473_299-1441d others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628866 | ||||||
| chr19:1628870
|
ACGGGGTG others(159): Show |
A | 1 | a0006c0012t0020g0262 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.299-1610_299-1445d others(2): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628870 | ||||||
| chr19:1628871
|
C | CAG | 65 | a0001c0002t0001g0173a0001c0002t0001g0181a0001c0002t0002g0188others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.299-1446_299-1445i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGAGGGT others(29): Show |
1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGAT others(29): Show |
1 | a0001c0002t0001g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGAT others(63): Show |
1 | a0001c0003t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(63): Show |
1 | a0001c0003t0001g0200 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(30): Show |
3 | a0001c0004t0001g0110a0001c0004t0002g0108a0001c0004t0002g0154 | 3 | HG02109.hp1 HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.299-1446_299-1445i others(39): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(268): Show |
1 | a0001c0004t0003g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(277): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(65): Show |
1 | a0001c0005t0047g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(74): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(751): Show |
1 | a0001c0004t0003g0109 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(760): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(305): Show |
1 | a0001c0005t0039g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(314): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(62): Show |
1 | a0002c0001t0088g0292 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CAGGGGGT others(98): Show |
1 | a0001c0005t0009g0016 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(107): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CG | 37 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0138others(34): Show | 37 | HG00544.hp1 HG00741.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.299-1446dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGGTG others(63): Show |
1 | a0001c0004t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGGTG others(96): Show |
1 | a0001c0002t0032g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGGTG others(132): Show |
4 | a0001c0004t0003g0105a0001c0004t0003g0106a0001c0004t0003g0280others(1): Show | 4 | HG00735.hp2 HG01123.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1446_299-1445i others(141): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGGTG others(29): Show |
1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGGTG others(130): Show |
1 | a0001c0005t0004g0017 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(163): Show |
1 | a0001c0004t0003g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(172): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(162): Show |
1 | a0002c0001t0019g0056 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(403): Show |
1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(412): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(28): Show |
1 | a0001c0005t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.299-1446_299-1445i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(404): Show |
1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(413): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(27): Show |
4 | a0002c0001t0006g0076a0002c0001t0019g0084a0002c0001t0073g0079others(1): Show | 4 | HG00408.hp1 NA19000.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1446_299-1445i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(876): Show |
1 | a0002c0001t0095g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(885): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(296): Show |
3 | a0001c0005t0009g0029a0002c0001t0006g0055a0002c0001t0007g0062 | 3 | HG02083.hp1 HG03834.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.299-1446_299-1445i others(305): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | CGGGGTGA others(768): Show |
1 | a0002c0001t0006g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.299-1446_299-1445i others(777): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | G | 2 | a0002c0001t0006g0083a0003c0006t0001g0128 | 2 | HG02683.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.299-1445G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628871
|
C | T | 4 | a0001c0002t0002g0186a0001c0002t0093g0341a0001c0004t0003g0099others(1): Show | 4 | HG00642.hp1 HG01192.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1445G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628871 | ||||||
| chr19:1628872
|
G | A | 2 | a0001c0005t0004g0030a0002c0001t0100g0342 | 2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.299-1446C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628872 | ||||||
| chr19:1628872
|
GGGGTGAG others(25): Show |
G | 2 | a0001c0004t0028g0101a0001c0007t0103g0351 | 2 | HG02258.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.299-1478_299-1447d others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628872 | ||||||
| chr19:1628875
|
G | A | 14 | a0001c0002t0075g0185a0001c0003t0001g0165a0001c0003t0002g0253others(11): Show | 14 | HG00099.hp1 HG00621.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.299-1449C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628875 | ||||||
| chr19:1628875
|
G | GA | 5 | a0001c0002t0001g0180a0001c0002t0058g0283a0001c0002t0093g0341others(2): Show | 5 | HG00642.hp1 HG01192.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1450_299-1449i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628875 | ||||||
| chr19:1628875
|
G | GTGAGGCG others(567): Show |
1 | a0001c0002t0065g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.299-1450_299-1449i others(576): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628875 | ||||||
| chr19:1628875
|
G | GTGAGGCG others(228): Show |
1 | a0001c0002t0002g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.299-1450_299-1449i others(237): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628875 | ||||||
| chr19:1628878
|
A | AGGCGGGA others(164): Show |
3 | a0003c0006t0001g0125a0003c0006t0002g0077a0003c0006t0010g0124 | 3 | HG00558.hp2 NA18612.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.299-1453_299-1452i others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628878 | ||||||
| chr19:1628878
|
A | AGGCGGGA others(611): Show |
1 | a0014c0020t0034g0316 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.299-1453_299-1452i others(620): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628878 | ||||||
| chr19:1628878
|
A | G | 16 | a0001c0002t0093g0341a0001c0004t0002g0257a0001c0004t0003g0099others(13): Show | 16 | HG00642.hp1 HG01192.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.299-1452T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628878 | ||||||
| chr19:1628879
|
G | A | 3 | a0001c0004t0002g0257a0002c0001t0070g0121a0003c0006t0001g0128 | 3 | HG01975.hp1 HG02683.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.299-1453C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628879 | ||||||
| chr19:1628879
|
G | C | 1 | a0004c0033t0036g0350 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.299-1453C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628879 | ||||||
| chr19:1628879
|
G | T | 1 | a0003c0006t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-1453C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628879 | ||||||
| chr19:1628881
|
C | T | 31 | a0001c0002t0001g0138a0001c0002t0002g0133a0001c0002t0032g0161others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.299-1455G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628881 | ||||||
| chr19:1628883
|
G | T | 2 | a0002c0001t0070g0121a0003c0006t0001g0128 | 2 | HG02683.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.299-1457C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628883 | ||||||
| chr19:1628887
|
G | A | 12 | a0001c0002t0001g0132a0001c0003t0002g0094a0001c0004t0001g0110others(9): Show | 12 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-1461C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628887 | ||||||
| chr19:1628895
|
C | A | 1 | a0003c0008t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299-1469G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628895 | ||||||
| chr19:1628895
|
C | T | 10 | a0001c0003t0059g0187a0001c0007t0002g0127a0001c0007t0012g0323others(7): Show | 10 | HG00423.hp2 HG02071.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-1469G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628895 | ||||||
| chr19:1628899
|
A | ACTCACGG others(1505): Show |
1 | a0001c0002t0002g0219 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.299-1474_299-1473i others(1514): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628899 | ||||||
| chr19:1628899
|
A | G | 218 | a0001c0002t0001g0078a0001c0002t0001g0138a0001c0002t0001g0173others(215): Show | 218 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.299-1473T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628899 | ||||||
| chr19:1628901
|
T | TCATGGGG others(266): Show |
2 | a0001c0003t0001g0096a0001c0003t0002g0247 | 2 | HG01943.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.299-1476_299-1475i others(275): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628901 | ||||||
| chr19:1628903
|
A | AT | 16 | a0001c0007t0001g0217a0002c0001t0006g0063a0002c0001t0006g0067others(13): Show | 16 | HG00642.hp2 HG00673.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-1478_299-1477i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628903 | ||||||
| chr19:1628904
|
C | CAG | 35 | a0001c0002t0001g0180a0001c0002t0002g0267a0001c0002t0005g0330others(32): Show | 35 | HG00408.hp2 HG00597.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.299-1479_299-1478i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | CAGGGGGT others(407): Show |
1 | a0001c0007t0002g0049 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.299-1479_299-1478i others(416): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | CAGGGGGT others(62): Show |
1 | a0001c0005t0002g0224 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.299-1479_299-1478i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | CG | 39 | a0001c0002t0001g0203a0001c0002t0002g0133a0001c0002t0002g0202others(36): Show | 39 | HG00423.hp2 HG00642.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.299-1479dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | CGGGGGTG others(98): Show |
1 | a0003c0006t0001g0116 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.299-1479_299-1478i others(107): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | CGGGGTGA others(736): Show |
1 | a0002c0001t0007g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-1479_299-1478i others(745): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | CGGGGTGA others(27): Show |
1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.299-1479_299-1478i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | G | 22 | a0001c0003t0001g0096a0001c0003t0001g0228a0001c0003t0002g0247others(19): Show | 22 | HG00639.hp2 HG00642.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-1478G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628904
|
C | T | 2 | a0002c0001t0070g0121a0003c0006t0001g0128 | 2 | HG02683.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.299-1478G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628904 | ||||||
| chr19:1628905
|
G | GGGGGTGA others(62): Show |
1 | a0004c0014t0079g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.299-1480_299-1479i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628905 | ||||||
| chr19:1628908
|
G | A | 7 | a0001c0003t0002g0243a0001c0004t0008g0103a0001c0004t0102g0344others(4): Show | 7 | HG00408.hp2 HG01069.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-1482C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628908 | ||||||
| chr19:1628908
|
G | GA | 3 | a0002c0001t0070g0121a0003c0006t0001g0128a0003c0006t0012g0313 | 3 | HG00544.hp1 HG02683.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.299-1483_299-1482i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628908 | ||||||
| chr19:1628908
|
G | GGTGGGGC others(29): Show |
1 | a0002c0001t0034g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.299-1483_299-1482i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628908 | ||||||
| chr19:1628911
|
A | AGGTGGGA others(161): Show |
1 | a0001c0005t0017g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.299-1486_299-1485i others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628911 | ||||||
| chr19:1628911
|
A | G | 28 | a0001c0002t0001g0138a0001c0002t0005g0319a0001c0002t0032g0161others(25): Show | 28 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.299-1485T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628911 | ||||||
| chr19:1628912
|
G | A | 5 | a0001c0013t0042g0033a0002c0001t0015g0088a0003c0006t0002g0123others(2): Show | 5 | HG01175.hp1 HG02056.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1486C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628912 | ||||||
| chr19:1628912
|
G | GGTGGGAA others(164): Show |
1 | a0002c0001t0007g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.299-1487_299-1486i others(173): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628912 | ||||||
| chr19:1628912
|
G | T | 1 | a0003c0006t0017g0294 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.299-1486C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628912 | ||||||
| chr19:1628914
|
C | T | 14 | a0001c0002t0002g0133a0001c0002t0085g0304a0001c0003t0002g0095others(11): Show | 14 | HG00621.hp1 HG00639.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-1488G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628914 | ||||||
| chr19:1628916
|
G | T | 4 | a0001c0013t0042g0033a0003c0006t0002g0123a0003c0006t0012g0314others(1): Show | 4 | HG01175.hp1 HG02056.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1490C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628916 | ||||||
| chr19:1628920
|
G | A | 8 | a0001c0003t0001g0152a0001c0003t0001g0226a0001c0003t0001g0228others(5): Show | 8 | HG00639.hp2 HG00738.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1494C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628920 | ||||||
| chr19:1628928
|
C | A | 3 | a0002c0001t0070g0121a0003c0006t0001g0128a0003c0006t0012g0313 | 3 | HG00544.hp1 HG02683.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.299-1502G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628928 | ||||||
| chr19:1628928
|
C | T | 10 | a0001c0007t0074g0090a0001c0007t0096g0311a0001c0025t0010g0266others(7): Show | 10 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-1502G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628928 | ||||||
| chr19:1628932
|
G | A | 35 | a0001c0002t0002g0267a0001c0002t0035g0349a0001c0003t0005g0325others(32): Show | 35 | HG00609.hp1 HG00642.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.299-1506C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628932 | ||||||
| chr19:1628932
|
G | GCTCACGG others(331): Show |
1 | a0003c0006t0012g0329 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299-1507_299-1506i others(340): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628932 | ||||||
| chr19:1628932
|
G | GCTCATGG others(27): Show |
1 | a0002c0001t0006g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.299-1507_299-1506i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628932 | ||||||
| chr19:1628937
|
C | CAG | 73 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0173others(70): Show | 73 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.299-1512_299-1511i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CAGGGGAT others(64): Show |
1 | a0001c0002t0001g0203 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.299-1512_299-1511i others(73): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CAGGGGGT others(510): Show |
1 | a0003c0006t0002g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.299-1512_299-1511i others(519): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CAGGGGGT others(168): Show |
1 | a0001c0005t0004g0017 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.299-1512_299-1511i others(177): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CAGGGGGT others(237): Show |
1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-1512_299-1511i others(246): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CAGGGGGT others(236): Show |
1 | a0003c0006t0001g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.299-1512_299-1511i others(245): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CG | 18 | a0001c0002t0001g0138a0001c0002t0002g0267a0001c0004t0001g0110others(15): Show | 18 | HG00140.hp2 HG00408.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.299-1512dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CGGGGGTG others(96): Show |
1 | a0001c0004t0003g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.299-1512_299-1511i others(105): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CGGGGGTG others(439): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-1512_299-1511i others(448): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CGGGGGTG others(1571): Show |
1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-1512_299-1511i others(1580): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CGGGGTGA others(62): Show |
2 | a0001c0004t0003g0286a0001c0004t0008g0256 | 2 | HG00735.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.299-1580_299-1512d others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | CGGGGTGG others(442): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-1512_299-1511i others(451): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | G | 2 | a0001c0003t0028g0144a0002c0001t0015g0081 | 2 | HG02004.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.299-1511G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628937
|
C | T | 4 | a0001c0007t0003g0107a0003c0006t0002g0123a0003c0006t0012g0314others(1): Show | 4 | HG02056.hp2 HG02717.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1511G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628937 | ||||||
| chr19:1628938
|
G | A | 2 | a0001c0007t0074g0090a0001c0007t0096g0311 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.299-1512C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628938 | ||||||
| chr19:1628938
|
G | GGGGGTGA others(29): Show |
1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.299-1513_299-1512i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628938 | ||||||
| chr19:1628941
|
G | A | 4 | a0001c0003t0002g0242a0001c0004t0008g0097a0001c0004t0008g0100others(1): Show | 4 | HG00639.hp1 HG01099.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1515C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628941 | ||||||
| chr19:1628941
|
G | GA | 8 | a0001c0007t0002g0149a0001c0007t0003g0107a0002c0001t0019g0284others(5): Show | 8 | HG02027.hp2 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1516_299-1515i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628941 | ||||||
| chr19:1628941
|
G | GATGGGGT others(95): Show |
1 | a0001c0002t0005g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.299-1516_299-1515i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628941 | ||||||
| chr19:1628944
|
A | AGGTGGGA others(27): Show |
2 | a0002c0001t0007g0071a0002c0001t0084g0290 | 2 | NA18990.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.299-1519_299-1518i others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628944 | ||||||
| chr19:1628944
|
A | G | 34 | a0001c0002t0001g0138a0001c0002t0001g0203a0001c0002t0093g0341others(31): Show | 34 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.299-1518T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628944 | ||||||
| chr19:1628945
|
G | A | 3 | a0001c0003t0002g0094a0001c0004t0011g0102a0003c0008t0001g0118 | 3 | HG02602.hp2 HG02735.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.299-1519C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628945 | ||||||
| chr19:1628945
|
G | C | 1 | a0004c0014t0079g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.299-1519C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628945 | ||||||
| chr19:1628947
|
C | T | 23 | a0001c0002t0001g0203a0001c0002t0005g0330a0001c0002t0032g0161others(20): Show | 23 | HG00280.hp2 HG00621.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.299-1521G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628947 | ||||||
| chr19:1628947
|
C | TGGGAAGG others(129): Show |
1 | a0003c0011t0063g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.299-1521_299-1520i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628947 | ||||||
| chr19:1628948
|
G | A | 3 | a0002c0001t0007g0064a0002c0001t0007g0071a0002c0001t0084g0290 | 3 | NA18990.hp1 NA19065.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.299-1522C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628948 | ||||||
| chr19:1628949
|
G | T | 1 | a0003c0008t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.299-1523C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628949 | ||||||
| chr19:1628950
|
G | A | 1 | a0001c0004t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299-1524C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628950 | ||||||
| chr19:1628960
|
G | C | 1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-1534C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628960 | ||||||
| chr19:1628961
|
C | A | 6 | a0001c0007t0002g0149a0003c0006t0002g0114a0003c0006t0002g0123others(3): Show | 6 | HG02027.hp2 HG02056.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1535G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628961 | ||||||
| chr19:1628961
|
C | T | 7 | a0001c0003t0028g0144a0001c0004t0003g0279a0002c0001t0064g0053others(4): Show | 7 | HG00323.hp1 HG02148.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-1535G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628961 | ||||||
| chr19:1628965
|
G | A | 2 | a0001c0004t0086g0303a0002c0001t0019g0284 | 2 | HG01993.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.299-1539C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628965 | ||||||
| chr19:1628969
|
A | ACGGGGGT others(56): Show |
1 | a0004c0014t0079g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.299-1544_299-1543i others(65): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628969 | ||||||
| chr19:1628969
|
A | ACGGGGTG others(93): Show |
2 | a0001c0007t0002g0149a0003c0006t0002g0114 | 2 | HG02027.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.299-1544_299-1543i others(102): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628969 | ||||||
| chr19:1628969
|
A | ACGGGGTG others(401): Show |
1 | a0002c0001t0019g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.299-1544_299-1543i others(410): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628969 | ||||||
| chr19:1628969
|
A | ATGGGGAT others(128): Show |
2 | a0001c0004t0001g0110a0001c0004t0002g0154 | 2 | HG02109.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.299-1544_299-1543i others(137): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628969 | ||||||
| chr19:1628969
|
A | G | 14 | a0001c0005t0009g0029a0002c0001t0006g0055a0002c0001t0006g0076others(11): Show | 14 | HG00408.hp1 HG00609.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-1543T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628969 | ||||||
| chr19:1628969
|
AC | A | 3 | a0001c0004t0062g0046a0001c0007t0002g0282a0003c0008t0001g0118 | 3 | HG02735.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.299-1544delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628969 | ||||||
| chr19:1628970
|
C | CGGGGTGG others(60): Show |
1 | a0004c0033t0036g0350 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.299-1545_299-1544i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628970 | ||||||
| chr19:1628970
|
CA | C | 20 | a0001c0002t0001g0138a0001c0003t0002g0095a0001c0003t0002g0243others(17): Show | 20 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.299-1545delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628970 | ||||||
| chr19:1628970
|
CAG | C | 22 | a0001c0002t0032g0161a0001c0002t0075g0185a0001c0003t0002g0287others(19): Show | 22 | HG01069.hp2 HG01167.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.299-1546_299-1545d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628970 | ||||||
| chr19:1628971
|
A | AGGGGGTG others(540): Show |
1 | a0001c0003t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-1546_299-1545i others(549): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628971 | ||||||
| chr19:1628971
|
A | G | 1 | a0001c0003t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.299-1545T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628971 | ||||||
| chr19:1628971
|
A | T | 4 | a0001c0004t0062g0046a0001c0007t0002g0282a0003c0008t0001g0118others(1): Show | 4 | HG01109.hp2 HG02735.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1545T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628971 | ||||||
| chr19:1628972
|
G | C | 4 | a0001c0007t0002g0149a0002c0001t0019g0284a0003c0006t0002g0114others(1): Show | 4 | HG02027.hp2 HG02056.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1546C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628972 | ||||||
| chr19:1628972
|
G | GGGGATGA others(332): Show |
1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-1547_299-1546i others(341): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628972 | ||||||
| chr19:1628972
|
G | GGGGGTGA others(297): Show |
1 | a0001c0002t0002g0133 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.299-1547_299-1546i others(306): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628972 | ||||||
| chr19:1628972
|
G | GGGGGTGA others(438): Show |
1 | a0003c0006t0031g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.299-1547_299-1546i others(447): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628972 | ||||||
| chr19:1628973
|
G | A | 4 | a0001c0003t0028g0144a0001c0004t0003g0279a0002c0001t0064g0053others(1): Show | 4 | HG02148.hp1 HG02615.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1547C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628973 | ||||||
| chr19:1628976
|
G | A | 32 | a0001c0002t0001g0111a0001c0002t0001g0173a0001c0002t0001g0174others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.299-1550C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628976 | ||||||
| chr19:1628979
|
A | AGGCGGGA others(232): Show |
1 | a0001c0004t0003g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299-1554_299-1553i others(241): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628979 | ||||||
| chr19:1628979
|
A | G | 30 | a0001c0002t0001g0138a0001c0003t0008g0098a0001c0003t0028g0144others(27): Show | 30 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.299-1553T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628979 | ||||||
| chr19:1628980
|
G | A | 10 | a0001c0004t0003g0044a0001c0004t0028g0101a0001c0004t0099g0343others(7): Show | 10 | HG00544.hp1 HG00597.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-1554C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628980 | ||||||
| chr19:1628980
|
G | T | 1 | a0003c0006t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.299-1554C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628980 | ||||||
| chr19:1628982
|
C | CGGGAAGG others(1910): Show |
1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.299-1557_299-1556i others(1919): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628982 | ||||||
| chr19:1628982
|
C | T | 8 | a0001c0004t0003g0279a0001c0004t0008g0097a0001c0004t0008g0100others(5): Show | 8 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1556G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628982 | ||||||
| chr19:1628983
|
G | A | 2 | a0002c0001t0029g0159a0002c0001t0054g0157 | 2 | HG00738.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.299-1557C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628983 | ||||||
| chr19:1628984
|
G | T | 4 | a0002c0001t0015g0088a0002c0001t0070g0121a0003c0006t0001g0128others(1): Show | 4 | HG00544.hp1 HG02683.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1558C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628984 | ||||||
| chr19:1628985
|
G | A | 15 | a0001c0004t0001g0166a0001c0005t0009g0029a0002c0001t0006g0055others(12): Show | 15 | HG00609.hp2 HG00673.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.299-1559C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628985 | ||||||
| chr19:1628985
|
G | GAAGGGGA others(229): Show |
1 | a0001c0005t0017g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.299-1560_299-1559i others(238): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628985 | ||||||
| chr19:1628996
|
C | T | 11 | a0001c0003t0059g0187a0001c0025t0010g0266a0003c0006t0001g0115others(8): Show | 11 | HG00323.hp1 HG00597.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-1570G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1628996 | ||||||
| chr19:1629000
|
G | A | 15 | a0001c0002t0002g0267a0001c0003t0002g0287a0001c0004t0011g0102others(12): Show | 15 | HG00621.hp1 HG01346.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-1574C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629000 | ||||||
| chr19:1629004
|
A | G | 12 | a0001c0005t0002g0224a0002c0001t0006g0063a0002c0001t0006g0067others(9): Show | 12 | HG00609.hp1 HG02132.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-1578T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629004 | ||||||
| chr19:1629004
|
ACGGGGGT others(25): Show |
A | 1 | a0001c0013t0037g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.299-1610_299-1579d others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629004 | ||||||
| chr19:1629005
|
C | CA | 48 | a0001c0002t0001g0138a0001c0002t0001g0178a0001c0002t0005g0319others(45): Show | 48 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.299-1580_299-1579i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
C | CAGGGGGT others(97): Show |
1 | a0001c0005t0002g0224 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.299-1580_299-1579i others(106): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
C | CAGGGGGT others(95): Show |
1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-1580_299-1579i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
C | CAGGGGGT others(978): Show |
1 | a0002c0001t0053g0057 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.299-1580_299-1579i others(987): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
C | CAGGGGGT others(809): Show |
1 | a0002c0001t0014g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.299-1580_299-1579i others(818): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
C | CGGGGTGA others(476): Show |
1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-1580_299-1579i others(485): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
C | CGGGGTGA others(265): Show |
1 | a0001c0004t0008g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.299-1580_299-1579i others(274): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
C | T | 10 | a0001c0002t0075g0185a0001c0003t0002g0094a0001c0007t0103g0351others(7): Show | 10 | HG00544.hp1 HG02258.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-1579G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629005
|
CG | C | 23 | a0001c0002t0001g0174a0001c0002t0002g0175a0001c0002t0002g0184others(20): Show | 23 | HG00597.hp1 HG01069.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.299-1580delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629005 | ||||||
| chr19:1629006
|
G | C | 1 | a0003c0006t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-1580C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629006 | ||||||
| chr19:1629006
|
G | GGGGGTGA others(60): Show |
2 | a0001c0007t0002g0278a0001c0007t0012g0335 | 2 | NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.299-1581_299-1580i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629006 | ||||||
| chr19:1629006
|
G | GGGGTGAG others(161): Show |
1 | a0001c0007t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-1581_299-1580i others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629006 | ||||||
| chr19:1629006
|
G | GGGGTGAG others(573): Show |
1 | a0001c0002t0005g0330 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.299-1581_299-1580i others(582): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629006 | ||||||
| chr19:1629006
|
G | GGGGTGAG others(365): Show |
1 | a0001c0002t0001g0132 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.299-1581_299-1580i others(374): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629006 | ||||||
| chr19:1629006
|
GGGGGTGA others(26): Show |
G | 1 | a0001c0002t0002g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.299-1613_299-1581d others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629006 | ||||||
| chr19:1629007
|
G | A | 2 | a0003c0006t0002g0123a0003c0006t0017g0297 | 2 | NA18989.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.299-1581C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629007 | ||||||
| chr19:1629007
|
G | GGGGTGGG others(62): Show |
2 | a0002c0001t0006g0075a0002c0001t0022g0318 | 2 | HG00621.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.299-1582_299-1581i others(71): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629007 | ||||||
| chr19:1629008
|
G | C | 2 | a0001c0002t0001g0218a0001c0002t0083g0307 | 2 | HG01981.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.299-1582C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629008 | ||||||
| chr19:1629010
|
G | A | 17 | a0001c0002t0001g0111a0001c0002t0035g0349a0001c0003t0002g0094others(14): Show | 17 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-1584C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629010 | ||||||
| chr19:1629013
|
A | AGGCGGGA others(61): Show |
1 | a0002c0001t0015g0088 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.299-1588_299-1587i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629013 | ||||||
| chr19:1629013
|
A | G | 39 | a0001c0002t0001g0138a0001c0002t0002g0133a0001c0002t0032g0161others(36): Show | 39 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.299-1587T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629013 | ||||||
| chr19:1629014
|
G | A | 7 | a0001c0002t0001g0138a0003c0006t0001g0128a0003c0006t0002g0114others(4): Show | 7 | HG02027.hp2 HG02056.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-1588C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629014 | ||||||
| chr19:1629014
|
G | GGCGGGAA others(28): Show |
1 | a0001c0007t0003g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-1589_299-1588i others(37): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629014 | ||||||
| chr19:1629014
|
G | GGCGGGAA others(303): Show |
1 | a0002c0001t0064g0053 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.299-1589_299-1588i others(312): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629014 | ||||||
| chr19:1629014
|
G | T | 1 | a0003c0006t0035g0345 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.299-1588C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629014 | ||||||
| chr19:1629016
|
C | T | 9 | a0001c0002t0001g0111a0001c0004t0066g0172a0001c0007t0103g0351others(6): Show | 9 | HG01069.hp2 HG02258.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-1590G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629016 | ||||||
| chr19:1629018
|
G | T | 6 | a0003c0006t0001g0128a0003c0006t0002g0114a0003c0006t0002g0123others(3): Show | 6 | HG02027.hp2 HG02056.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1592C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629018 | ||||||
| chr19:1629019
|
G | A | 9 | a0002c0001t0006g0063a0002c0001t0006g0067a0002c0001t0006g0068others(6): Show | 9 | HG02132.hp1 NA18612.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-1593C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629019 | ||||||
| chr19:1629022
|
G | A | 8 | a0001c0003t0002g0275a0001c0004t0002g0108a0001c0004t0003g0104others(5): Show | 8 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-1596C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629022 | ||||||
| chr19:1629030
|
C | A | 2 | a0003c0006t0012g0313a0004c0014t0079g0305 | 2 | HG00544.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.299-1604G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629030 | ||||||
| chr19:1629030
|
C | T | 7 | a0001c0025t0010g0266a0003c0006t0001g0115a0003c0006t0001g0116others(4): Show | 7 | HG00323.hp1 NA18964.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-1604G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629030 | ||||||
| chr19:1629034
|
G | A | 19 | a0001c0002t0001g0178a0001c0002t0075g0185a0001c0003t0002g0247others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.299-1608C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629034 | ||||||
| chr19:1629038
|
ACGGGGTG others(24): Show |
A | 1 | a0001c0004t0011g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.299-1643_299-1613d others(33): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629038 | ||||||
| chr19:1629039
|
C | CAG | 36 | a0001c0002t0002g0267a0001c0003t0002g0242a0001c0003t0002g0243others(33): Show | 36 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.299-1614_299-1613i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629039 | ||||||
| chr19:1629039
|
C | CG | 38 | a0001c0002t0001g0132a0001c0002t0005g0319a0001c0002t0005g0330others(35): Show | 38 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.299-1614dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629039 | ||||||
| chr19:1629039
|
C | G | 5 | a0001c0009t0050g0168a0001c0013t0037g0009a0002c0001t0007g0070others(2): Show | 5 | HG01884.hp2 HG02895.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1613G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629039 | ||||||
| chr19:1629039
|
C | T | 9 | a0001c0002t0002g0186a0001c0004t0099g0343a0002c0001t0070g0121others(6): Show | 9 | HG00597.hp1 HG02027.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-1613G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629039 | ||||||
| chr19:1629039
|
CGGGGTGA others(60): Show |
C | 3 | a0001c0007t0103g0351a0002c0001t0100g0342a0003c0008t0001g0118 | 3 | HG02258.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.299-1680_299-1614d others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629039 | ||||||
| chr19:1629043
|
G | A | 4 | a0001c0002t0002g0267a0001c0003t0002g0253a0001c0007t0071g0199others(1): Show | 4 | HG02083.hp1 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1617C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629043 | ||||||
| chr19:1629043
|
G | GA | 16 | a0001c0004t0099g0343a0001c0007t0002g0127a0001c0007t0012g0323others(13): Show | 16 | HG00597.hp1 HG02027.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-1618_299-1617i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629043 | ||||||
| chr19:1629046
|
A | AGGCGGGA others(297): Show |
1 | a0001c0002t0002g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.299-1621_299-1620i others(306): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629046 | ||||||
| chr19:1629046
|
A | AGGCGGGA others(597): Show |
1 | a0001c0002t0065g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.299-1621_299-1620i others(606): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629046 | ||||||
| chr19:1629046
|
A | AGGCGGGA others(1310): Show |
1 | a0001c0002t0002g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.299-1621_299-1620i others(1319): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629046 | ||||||
| chr19:1629046
|
A | G | 46 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0005g0319others(43): Show | 46 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.299-1620T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629046 | ||||||
| chr19:1629047
|
G | A | 8 | a0001c0003t0028g0144a0001c0007t0002g0282a0001c0007t0074g0090others(5): Show | 8 | HG01192.hp2 HG01884.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-1621C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629047 | ||||||
| chr19:1629049
|
C | T | 21 | a0001c0002t0002g0133a0001c0002t0032g0161a0001c0003t0002g0095others(18): Show | 21 | HG00408.hp2 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-1623G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629049 | ||||||
| chr19:1629050
|
G | A | 1 | a0002c0001t0088g0292 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.299-1624C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629050 | ||||||
| chr19:1629052
|
G | A | 1 | a0002c0001t0006g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.299-1626C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629052 | ||||||
| chr19:1629063
|
C | A | 8 | a0001c0004t0066g0172a0001c0007t0002g0127a0002c0001t0001g0122others(5): Show | 8 | HG02071.hp1 HG03704.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-1637G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629063 | ||||||
| chr19:1629063
|
C | T | 3 | a0001c0004t0003g0220a0001c0007t0020g0289a0003c0006t0001g0092 | 3 | HG01243.hp2 HG01891.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.299-1637G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629063 | ||||||
| chr19:1629067
|
G | A | 7 | a0001c0002t0036g0348a0001c0004t0008g0151a0001c0005t0009g0029others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-1641C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629067 | ||||||
| chr19:1629072
|
C | CAG | 41 | a0001c0002t0001g0138a0001c0002t0001g0173a0001c0002t0001g0174others(38): Show | 41 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.299-1647_299-1646i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629072 | ||||||
| chr19:1629072
|
C | CAGGGGGT others(29): Show |
1 | a0001c0003t0002g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.299-1647_299-1646i others(38): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629072 | ||||||
| chr19:1629072
|
C | CAGGGGGT others(63): Show |
1 | a0003c0006t0012g0313 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.299-1647_299-1646i others(72): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629072 | ||||||
| chr19:1629072
|
C | CG | 36 | a0001c0002t0001g0180a0001c0002t0036g0348a0001c0003t0002g0243others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.299-1647dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629072 | ||||||
| chr19:1629072
|
C | G | 1 | a0001c0004t0011g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.299-1646G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629072 | ||||||
| chr19:1629072
|
C | T | 20 | a0001c0003t0009g0007a0001c0003t0028g0144a0001c0004t0066g0172others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.299-1646G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629072 | ||||||
| chr19:1629072
|
CGGGGTGA others(27): Show |
C | 1 | a0002c0001t0070g0121 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.299-1680_299-1647d others(36): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629072 | ||||||
| chr19:1629073
|
G | A | 2 | a0001c0004t0003g0220a0001c0007t0020g0289 | 2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.299-1647C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629073 | ||||||
| chr19:1629076
|
G | A | 4 | a0001c0002t0002g0184a0002c0001t0073g0079a0002c0001t0088g0292others(1): Show | 4 | HG00544.hp1 HG00609.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1650C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629076 | ||||||
| chr19:1629076
|
G | GA | 22 | a0001c0003t0009g0007a0001c0003t0028g0144a0001c0003t0059g0187others(19): Show | 22 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.299-1651_299-1650i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629076 | ||||||
| chr19:1629076
|
G | GATGGGGT others(60): Show |
1 | a0001c0002t0005g0319 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.299-1651_299-1650i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629076 | ||||||
| chr19:1629076
|
G | GGTGGGGC others(264): Show |
1 | a0001c0002t0035g0349 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299-1651_299-1650i others(273): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629076 | ||||||
| chr19:1629079
|
A | AGGTGGGA others(302): Show |
1 | a0002c0001t0029g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.299-1654_299-1653i others(311): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629079 | ||||||
| chr19:1629079
|
A | AGGTGGGA others(437): Show |
1 | a0002c0001t0057g0158 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.299-1654_299-1653i others(446): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629079 | ||||||
| chr19:1629079
|
A | G | 42 | a0001c0002t0001g0138a0001c0002t0001g0180a0001c0002t0005g0319others(39): Show | 42 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.299-1653T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629079 | ||||||
| chr19:1629080
|
G | A | 9 | a0001c0002t0001g0138a0001c0004t0001g0110a0001c0004t0002g0154others(6): Show | 9 | HG00621.hp1 HG01109.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.299-1654C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629080 | ||||||
| chr19:1629080
|
G | GGTGGGAA others(608): Show |
1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.299-1655_299-1654i others(617): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629080 | ||||||
| chr19:1629080
|
G | GGTGGGAA others(403): Show |
1 | a0001c0004t0008g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.299-1655_299-1654i others(412): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629080 | ||||||
| chr19:1629080
|
G | GGTGGGAA others(301): Show |
3 | a0001c0004t0003g0105a0001c0004t0003g0106a0001c0004t0011g0145 | 3 | HG00735.hp2 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.299-1655_299-1654i others(310): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629080 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(160): Show |
2 | a0001c0003t0001g0200a0001c0003t0001g0201 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.299-1657_299-1656i others(169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(504): Show |
1 | a0001c0002t0001g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.299-1657_299-1656i others(513): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(367): Show |
1 | a0001c0002t0036g0348 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-1657_299-1656i others(376): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(638): Show |
1 | a0001c0002t0001g0198 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-1657_299-1656i others(647): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(399): Show |
1 | a0012c0030t0002g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.299-1657_299-1656i others(408): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(635): Show |
1 | a0001c0002t0002g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-1657_299-1656i others(644): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(638): Show |
1 | a0001c0002t0002g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.299-1657_299-1656i others(647): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(1903): Show |
1 | a0001c0002t0002g0202 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-1657_299-1656i others(1912): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(911): Show |
1 | a0001c0005t0001g0183 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.299-1657_299-1656i others(920): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(2822): Show |
1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299-1657_299-1656i others(2831): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(837): Show |
1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.299-1657_299-1656i others(846): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(126): Show |
5 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0203others(2): Show | 5 | HG01192.hp1 HG01891.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1657_299-1656i others(135): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(59): Show |
1 | a0001c0002t0002g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-1657_299-1656i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | CGGGAAGG others(676): Show |
1 | a0002c0001t0069g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.299-1657_299-1656i others(685): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629082
|
C | T | 44 | a0001c0002t0001g0132a0001c0002t0005g0319a0001c0002t0005g0330others(41): Show | 44 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.299-1656G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629082 | ||||||
| chr19:1629096
|
C | A | 2 | a0001c0003t0059g0187a0017c0026t0002g0112 | 2 | HG00423.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.299-1670G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629096 | ||||||
| chr19:1629096
|
C | T | 5 | a0001c0025t0010g0266a0002c0001t0014g0087a0002c0001t0034g0309others(2): Show | 5 | HG00597.hp2 NA19063.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1670G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629096 | ||||||
| chr19:1629100
|
G | A | 8 | a0001c0003t0002g0094a0001c0004t0003g0279a0001c0004t0021g0321others(5): Show | 8 | HG02148.hp1 HG02602.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.299-1674C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629100 | ||||||
| chr19:1629105
|
C | CA | 3 | a0001c0003t0002g0247a0003c0006t0001g0119a0003c0006t0080g0296 | 3 | HG01943.hp2 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.299-1680_299-1679i others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAG | 14 | a0001c0002t0085g0304a0001c0004t0003g0099a0001c0004t0003g0285others(11): Show | 14 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-1680_299-1679i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAGAGGGT others(233): Show |
1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.299-1680_299-1679i others(242): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAGAGGGT others(130): Show |
1 | a0002c0001t0034g0309 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.299-1680_299-1679i others(139): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAGGGGGT others(129): Show |
1 | a0002c0001t0015g0088 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.299-1680_299-1679i others(138): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAGGGGGT others(61): Show |
1 | a0005c0010t0018g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.299-1680_299-1679i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAGGGGGT others(198): Show |
2 | a0001c0007t0002g0127a0001c0007t0012g0323 | 2 | HG02071.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.299-1680_299-1679i others(207): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAGGGGGT others(197): Show |
5 | a0002c0001t0001g0122a0003c0006t0002g0147a0003c0006t0010g0141others(2): Show | 5 | NA18947.hp2 NA18955.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1680_299-1679i others(206): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CAGGGGGT others(197): Show |
1 | a0003c0008t0001g0113 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.299-1680_299-1679i others(206): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | CG | 12 | a0001c0003t0001g0255a0001c0003t0002g0242a0001c0003t0002g0253others(9): Show | 12 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-1680dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | G | 1 | a0001c0007t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-1679G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
C | T | 5 | a0001c0002t0001g0138a0002c0001t0006g0075a0002c0001t0022g0318others(2): Show | 5 | HG00621.hp1 HG01109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-1679G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629105
|
CG | C | 40 | a0001c0002t0001g0181a0001c0003t0002g0243a0001c0003t0009g0007others(37): Show | 40 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.299-1680delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629105 | ||||||
| chr19:1629106
|
G | A | 1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-1680C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | C | 12 | a0001c0007t0002g0127a0001c0007t0012g0323a0002c0001t0001g0122others(9): Show | 12 | HG02071.hp1 HG03471.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-1680C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGATGG others(162): Show |
2 | a0003c0006t0001g0142a0003c0006t0031g0129 | 2 | NA18747.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(171): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGATGG others(26): Show |
3 | a0001c0002t0001g0138a0002c0001t0006g0075a0002c0001t0022g0318 | 3 | HG00621.hp1 HG02559.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(35): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(744): Show |
1 | a0001c0025t0010g0266 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.299-1681_299-1680i others(753): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(503): Show |
1 | a0001c0005t0017g0293 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.299-1681_299-1680i others(512): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(402): Show |
3 | a0001c0004t0003g0091a0001c0004t0008g0097a0001c0004t0008g0100 | 3 | HG00140.hp2 HG00639.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(411): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(335): Show |
1 | a0001c0003t0002g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(344): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(1799): Show |
1 | a0001c0004t0002g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(1808): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(674): Show |
1 | a0001c0004t0003g0109 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(683): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(197): Show |
2 | a0001c0004t0003g0104a0001c0004t0003g0280 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(206): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGA others(774): Show |
1 | a0001c0004t0021g0312 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(783): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(198): Show |
1 | a0001c0005t0002g0224 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(207): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(1718): Show |
1 | a0001c0007t0002g0049 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(1727): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(400): Show |
1 | a0002c0001t0022g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(409): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(367): Show |
4 | a0002c0001t0016g0051a0002c0001t0016g0052a0002c0001t0016g0269others(1): Show | 4 | HG00642.hp2 HG01070.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1681_299-1680i others(376): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(367): Show |
1 | a0002c0001t0016g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.299-1681_299-1680i others(376): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(297): Show |
1 | a0002c0001t0007g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(306): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(876): Show |
3 | a0002c0001t0006g0055a0002c0001t0006g0089a0002c0001t0019g0056 | 3 | NA18944.hp2 NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(885): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(61): Show |
2 | a0001c0002t0002g0133a0001c0002t0032g0161 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(70): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(302): Show |
1 | a0001c0002t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299-1681_299-1680i others(311): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(95): Show |
2 | a0001c0005t0001g0223a0001c0007t0020g0289 | 2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(104): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(198): Show |
3 | a0002c0001t0007g0064a0002c0001t0007g0071a0002c0001t0084g0290 | 3 | NA18990.hp1 NA19065.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.299-1681_299-1680i others(207): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(939): Show |
1 | a0002c0001t0007g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299-1681_299-1680i others(948): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGGGTGG others(431): Show |
1 | a0010c0023t0051g0140 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-1681_299-1680i others(440): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629106
|
G | GGGTGGGG others(229): Show |
1 | a0006c0012t0020g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.299-1681_299-1680i others(238): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629106 | ||||||
| chr19:1629109
|
G | A | 3 | a0001c0002t0085g0304a0001c0004t0003g0285a0001c0005t0002g0131 | 3 | HG01106.hp2 HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.299-1683C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629109 | ||||||
| chr19:1629112
|
A | AGGCGGGA others(1356): Show |
1 | a0001c0003t0002g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(1365): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGCGGGA others(848): Show |
1 | a0003c0006t0001g0119 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(857): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGCGGGA others(883): Show |
1 | a0003c0006t0080g0296 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(892): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGCGGGA others(94): Show |
1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGCGGGA others(607): Show |
1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(616): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGCGGGA others(470): Show |
1 | a0003c0006t0001g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(479): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGCGGGA others(402): Show |
1 | a0003c0008t0068g0268 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(411): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(742): Show |
1 | a0001c0004t0003g0099 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(751): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(1247): Show |
1 | a0002c0001t0015g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(1256): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(398): Show |
1 | a0002c0001t0007g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(407): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(435): Show |
1 | a0001c0003t0008g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(444): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(741): Show |
1 | a0002c0001t0007g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(750): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(230): Show |
6 | a0001c0004t0003g0153a0001c0004t0011g0134a0001c0004t0011g0135others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.299-1687_299-1686i others(239): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(435): Show |
1 | a0002c0001t0092g0295 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(444): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(468): Show |
1 | a0002c0001t0006g0083 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(477): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(400): Show |
2 | a0002c0001t0006g0063a0002c0001t0006g0067 | 2 | NA18945.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.299-1687_299-1686i others(409): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(331): Show |
1 | a0002c0001t0006g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(340): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(435): Show |
1 | a0002c0001t0007g0060 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(444): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(1143): Show |
1 | a0002c0001t0007g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(1152): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(229): Show |
1 | a0002c0001t0088g0292 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(238): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | AGGTGGGA others(535): Show |
2 | a0002c0001t0019g0084a0013c0022t0007g0066 | 2 | NA19000.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.299-1687_299-1686i others(544): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | ATGCGGGA others(879): Show |
1 | a0001c0003t0002g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-1687_299-1686i others(888): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | ATGCGGGA others(749): Show |
1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-1687_299-1686i others(758): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629112
|
A | G | 101 | a0001c0002t0001g0138a0001c0002t0001g0180a0001c0002t0001g0181others(98): Show | 101 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.299-1686T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629112 | ||||||
| chr19:1629113
|
G | A | 2 | a0001c0004t0003g0220a0001c0005t0001g0223 | 2 | HG01243.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.299-1687C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629113 | ||||||
| chr19:1629113
|
G | GGCGGGAA others(191): Show |
1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-1688_299-1687i others(200): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629113 | ||||||
| chr19:1629113
|
G | GGCGGGAA others(264): Show |
1 | a0001c0004t0021g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.299-1688_299-1687i others(273): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629113 | ||||||
| chr19:1629113
|
G | GGCGGGAA others(60): Show |
1 | a0001c0004t0003g0279 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.299-1688_299-1687i others(69): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629113 | ||||||
| chr19:1629115
|
C | T | 1 | a0004c0033t0036g0350 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.299-1689G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629115 | ||||||
| chr19:1629129
|
C | A | 127 | a0001c0002t0001g0138a0001c0002t0001g0180a0001c0002t0001g0181others(124): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.299-1703G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAACTC others(811): Show |
1 | a0003c0011t0030g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(820): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAACTC others(331): Show |
2 | a0003c0006t0001g0160a0003c0006t0002g0120 | 2 | NA18971.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.299-1704_299-1703i others(340): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAACTC others(300): Show |
1 | a0002c0001t0054g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(309): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAACTC others(884): Show |
1 | a0002c0001t0007g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(893): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAACTC others(670): Show |
1 | a0001c0007t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(679): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAACTC others(3654): Show |
1 | a0001c0002t0085g0304 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(3663): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(233): Show |
1 | a0001c0003t0002g0253 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(242): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(647): Show |
1 | a0009c0021t0001g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(656): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(536): Show |
1 | a0002c0001t0073g0079 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(545): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(401): Show |
1 | a0003c0006t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(410): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(163): Show |
1 | a0001c0003t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(172): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(232): Show |
1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(241): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(2001): Show |
1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(2010): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(505): Show |
1 | a0003c0006t0017g0294 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(514): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(635): Show |
1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(644): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(94): Show |
1 | a0002c0001t0064g0053 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(230): Show |
3 | a0001c0003t0059g0187a0003c0006t0001g0148a0017c0026t0002g0112 | 3 | HG00423.hp2 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.299-1704_299-1703i others(239): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(196): Show |
1 | a0001c0003t0076g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(205): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(885): Show |
1 | a0003c0006t0035g0345 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(894): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(195): Show |
1 | a0003c0006t0001g0116 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(204): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(161): Show |
1 | a0004c0014t0079g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(170): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(1281): Show |
1 | a0002c0001t0006g0072 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(1290): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(437): Show |
1 | a0001c0003t0001g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(446): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(1160): Show |
1 | a0002c0001t0095g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(1169): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(1664): Show |
1 | a0002c0001t0014g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(1673): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(903): Show |
1 | a0002c0001t0022g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(912): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(94): Show |
2 | a0001c0002t0001g0132a0001c0002t0005g0330 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.299-1704_299-1703i others(103): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(839): Show |
1 | a0001c0004t0003g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(848): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(500): Show |
1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(509): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(1348): Show |
1 | a0002c0001t0015g0080 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(1357): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(849): Show |
1 | a0002c0001t0087g0291 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(858): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(917): Show |
1 | a0002c0001t0053g0057 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(926): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(915): Show |
1 | a0002c0001t0014g0059 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(924): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(672): Show |
1 | a0002c0001t0006g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(681): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(1559): Show |
1 | a0001c0004t0008g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(1568): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(882): Show |
1 | a0002c0001t0014g0058 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(891): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(704): Show |
1 | a0002c0001t0015g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(713): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(1060): Show |
1 | a0004c0014t0013g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(1069): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(568): Show |
1 | a0002c0001t0007g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(577): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(464): Show |
1 | a0001c0005t0009g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(473): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(1853): Show |
1 | a0002c0001t0029g0156 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.299-1704_299-1703i others(1862): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(25): Show |
4 | a0001c0003t0002g0242a0001c0007t0003g0107a0003c0006t0002g0126others(1): Show | 4 | HG00438.hp2 HG01109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-1704_299-1703i others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629129
|
C | CAGAGCTC others(59): Show |
1 | a0001c0003t0002g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.299-1704_299-1703i others(68): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629129 | ||||||
| chr19:1629171
|
C | T | 1 | a0003c0006t0012g0313 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.299-1745G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629171 | ||||||
| chr19:1629252
|
G | A | 3 | a0001c0004t0003g0220a0001c0004t0003g0279a0001c0004t0021g0321 | 3 | HG01243.hp2 HG02148.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.299-1826C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629252 | ||||||
| chr19:1629321
|
C | CGCACAGG others(16): Show |
3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.299-1896_299-1895i others(25): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629321 | ||||||
| chr19:1629321
|
C | G | 9 | a0001c0003t0001g0255a0001c0003t0002g0242a0001c0003t0002g0243others(6): Show | 9 | HG01192.hp2 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-1895G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629321 | ||||||
| chr19:1629357
|
T | C | 3 | a0001c0004t0011g0135a0001c0004t0011g0136a0001c0004t0011g0137 | 3 | HG00741.hp2 HG01074.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.299-1931A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629357 | ||||||
| chr19:1629367
|
G | C | 1 | a0001c0003t0005g0325 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.299-1941C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629367 | ||||||
| chr19:1629463
|
AG | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-2038delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629463 | ||||||
| chr19:1629469
|
T | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.299-2043A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629469 | ||||||
| chr19:1629532
|
A | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.299-2106T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629532 | ||||||
| chr19:1629621
|
G | A | 185 | a0001c0002t0001g0078a0001c0002t0001g0181a0001c0002t0001g0209others(182): Show | 185 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.299-2195C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629621 | ||||||
| chr19:1629621
|
G | C | 1 | a0003c0006t0017g0298 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299-2195C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629621 | ||||||
| chr19:1629744
|
G | C | 1 | a0001c0005t0004g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.298+2294C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629744 | ||||||
| chr19:1629866
|
G | A | 7 | a0001c0002t0046g0039a0001c0005t0004g0026a0001c0005t0009g0016others(4): Show | 7 | HG01109.hp1 NA18962.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.298+2172C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629866 | ||||||
| chr19:1629910
|
G | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+2128C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629910 | ||||||
| chr19:1629954
|
C | A | 1 | a0001c0002t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.298+2084G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1629954 | ||||||
| chr19:1630018
|
G | A | 23 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0002g0133others(20): Show | 23 | HG00735.hp2 HG01106.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.298+2020C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630018 | ||||||
| chr19:1630119
|
T | C | 65 | a0001c0002t0041g0004a0001c0005t0002g0224a0001c0005t0009g0029others(62): Show | 65 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.298+1919A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630119 | ||||||
| chr19:1630133
|
G | A | 63 | a0001c0002t0041g0004a0001c0005t0002g0224a0001c0005t0009g0029others(60): Show | 63 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.298+1905C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630133 | ||||||
| chr19:1630204
|
G | C | 1 | a0001c0009t0098g0347 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.298+1834C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630204 | ||||||
| chr19:1630273
|
C | T | 2 | a0001c0002t0001g0209a0001c0002t0001g0216 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.298+1765G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630273 | ||||||
| chr19:1630342
|
A | C | 194 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0138others(191): Show | 194 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.298+1696T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630342 | ||||||
| chr19:1630377
|
C | G | 2 | a0001c0007t0003g0107a0003c0011t0063g0093 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.298+1661G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630377 | ||||||
| chr19:1630404
|
G | T | 4 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(1): Show | 4 | HG01106.hp2 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1634C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630404 | ||||||
| chr19:1630406
|
G | A | 1 | a0001c0004t0003g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.298+1632C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630406 | ||||||
| chr19:1630525
|
G | A | 5 | a0001c0005t0004g0008a0004c0033t0036g0350a0005c0010t0018g0169others(2): Show | 5 | HG01109.hp2 HG01884.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+1513C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630525 | ||||||
| chr19:1630578
|
T | C | 2 | a0001c0005t0004g0011a0001c0005t0004g0027 | 2 | HG04115.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.298+1460A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630578 | ||||||
| chr19:1630679
|
G | A | 2 | a0001c0007t0020g0289a0003c0011t0030g0139 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.298+1359C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630679 | ||||||
| chr19:1630697
|
AGGATGAC others(4): Show |
A | 1 | a0001c0002t0001g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298+1330_298+1340d others(13): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630697 | ||||||
| chr19:1630754
|
T | C | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1284A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630754 | ||||||
| chr19:1630786
|
C | T | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+1252G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630786 | ||||||
| chr19:1630807
|
C | A | 2 | a0001c0007t0103g0351a0010c0023t0051g0140 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.298+1231G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630807 | ||||||
| chr19:1630843
|
G | A | 1 | a0001c0003t0005g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.298+1195C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630843 | ||||||
| chr19:1630889
|
C | T | 1 | a0001c0003t0076g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.298+1149G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630889 | ||||||
| chr19:1630940
|
C | T | 1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.298+1098G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630940 | ||||||
| chr19:1630962
|
G | A | 1 | a0005c0010t0018g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+1076C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630962 | ||||||
| chr19:1630995
|
G | A | 3 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170 | 3 | HG01109.hp2 HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.298+1043C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1630995 | ||||||
| chr19:1631134
|
T | C | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+904A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631134 | ||||||
| chr19:1631273
|
CT | C | 66 | a0001c0002t0001g0216a0001c0002t0002g0143a0001c0002t0065g0176others(63): Show | 66 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.298+764delA | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631273 | ||||||
| chr19:1631430
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.298+608C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631430 | ||||||
| chr19:1631458
|
G | A | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.298+580C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631458 | ||||||
| chr19:1631640
|
G | C | 1 | a0003c0011t0063g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.298+398C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631640 | ||||||
| chr19:1631678
|
C | T | 1 | a0003c0006t0033g0315 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.298+360G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631678 | ||||||
| chr19:1631821
|
G | A | 2 | a0001c0003t0059g0187a0003c0008t0068g0268 | 2 | HG00323.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.298+217C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631821 | ||||||
| chr19:1631878
|
TC | T | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+159delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 5/18 | chr19 | 1631878 | ||||||
| chr19:1632185
|
G | C | 2 | a0002c0001t0029g0159a0002c0001t0057g0158 | 2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.220-69C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 4/18 | chr19 | 1632185 | ||||||
| chr19:1632198
|
GA | G | 26 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(23): Show | 26 | HG00621.hp2 HG01081.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.220-83delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 4/18 | chr19 | 1632198 | ||||||
| chr19:1632320
|
G | A | 1 | a0002c0001t0084g0290 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.219+12C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 4/18 | chr19 | 1632320 | ||||||
| chr19:1632502
|
G | A | 2 | a0001c0007t0103g0351a0010c0023t0051g0140 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.146-97C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1632502 | ||||||
| chr19:1632542
|
C | A | 2 | a0001c0004t0003g0106a0001c0004t0011g0145 | 2 | HG00735.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.146-137G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1632542 | ||||||
| chr19:1632637
|
G | A | 5 | a0001c0007t0012g0323a0004c0033t0036g0350a0005c0010t0018g0169others(2): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-232C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1632637 | ||||||
| chr19:1633069
|
C | T | 1 | a0001c0007t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.146-664G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633069 | ||||||
| chr19:1633070
|
G | A | 3 | a0001c0002t0001g0271a0001c0002t0002g0270a0001c0002t0002g0272 | 3 | HG03654.hp1 HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.146-665C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633070 | ||||||
| chr19:1633099
|
C | A | 2 | a0001c0003t0001g0261a0007c0016t0002g0260 | 2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.146-694G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633099 | ||||||
| chr19:1633155
|
C | A | 1 | a0002c0001t0092g0295 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.146-750G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633155 | ||||||
| chr19:1633173
|
A | C | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-768T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633173 | ||||||
| chr19:1633204
|
G | A | 3 | a0001c0005t0004g0005a0001c0005t0040g0006a0001c0005t0047g0042 | 3 | HG03704.hp2 HG03831.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.146-799C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633204 | ||||||
| chr19:1633393
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-988C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633393 | ||||||
| chr19:1633424
|
G | C | 1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.146-1019C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633424 | ||||||
| chr19:1633509
|
G | A | 3 | a0002c0001t0006g0063a0002c0001t0007g0064a0002c0001t0034g0309 | 3 | NA19066.hp2 NA19077.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.146-1104C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633509 | ||||||
| chr19:1633529
|
C | T | 1 | a0001c0003t0001g0233 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.146-1124G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633529 | ||||||
| chr19:1633581
|
T | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-1176A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633581 | ||||||
| chr19:1633628
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1223G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633628 | ||||||
| chr19:1633666
|
A | C | 1 | a0002c0001t0006g0075 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.146-1261T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633666 | ||||||
| chr19:1633807
|
G | A | 33 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(30): Show | 33 | HG00621.hp2 HG01081.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.146-1402C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633807 | ||||||
| chr19:1633884
|
T | C | 129 | a0001c0002t0001g0132a0001c0002t0001g0138a0001c0002t0002g0133others(126): Show | 129 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.146-1479A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633884 | ||||||
| chr19:1633924
|
T | G | 62 | a0001c0005t0002g0224a0001c0005t0009g0029a0001c0005t0017g0293others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.146-1519A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1633924 | ||||||
| chr19:1634222
|
A | G | 1 | a0001c0002t0085g0304 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.146-1817T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1634222 | ||||||
| chr19:1634396
|
T | C | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1991A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1634396 | ||||||
| chr19:1634403
|
G | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-1998C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1634403 | ||||||
| chr19:1634596
|
T | C | 196 | a0001c0002t0001g0078a0001c0002t0001g0132a0001c0002t0001g0138others(193): Show | 196 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.146-2191A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1634596 | ||||||
| chr19:1634612
|
T | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-2207A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1634612 | ||||||
| chr19:1634656
|
G | C | 17 | a0001c0002t0001g0209a0001c0002t0001g0212a0001c0002t0001g0213others(14): Show | 17 | HG00621.hp2 HG01081.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.146-2251C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1634656 | ||||||
| chr19:1635090
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2685G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635090 | ||||||
| chr19:1635203
|
T | C | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2798A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635203 | ||||||
| chr19:1635316
|
T | C | 62 | a0001c0005t0002g0224a0001c0005t0009g0029a0001c0005t0017g0293others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.146-2911A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635316 | ||||||
| chr19:1635371
|
T | C | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2966A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635371 | ||||||
| chr19:1635422
|
C | G | 1 | a0001c0003t0002g0275 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.146-3017G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635422 | ||||||
| chr19:1635550
|
T | C | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3145A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635550 | ||||||
| chr19:1635695
|
A | G | 1 | a0002c0001t0019g0056 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.146-3290T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635695 | ||||||
| chr19:1635737
|
A | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-3332T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635737 | ||||||
| chr19:1635764
|
T | C | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3359A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635764 | ||||||
| chr19:1635960
|
C | T | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3555G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1635960 | ||||||
| chr19:1636006
|
G | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-3601C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636006 | ||||||
| chr19:1636082
|
T | C | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-3677A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636082 | ||||||
| chr19:1636163
|
T | A | 62 | a0001c0004t0002g0257a0001c0005t0002g0224a0001c0005t0009g0029others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.146-3758A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636163 | ||||||
| chr19:1636272
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-3867C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636272 | ||||||
| chr19:1636287
|
G | A | 1 | a0001c0005t0009g0024 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.146-3882C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636287 | ||||||
| chr19:1636654
|
G | A | 1 | a0001c0007t0005g0339 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.146-4249C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636654 | ||||||
| chr19:1636752
|
C | G | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-4347G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636752 | ||||||
| chr19:1636811
|
C | G | 1 | a0001c0004t0102g0344 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.146-4406G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636811 | ||||||
| chr19:1636837
|
G | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-4432C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636837 | ||||||
| chr19:1636857
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-4452G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636857 | ||||||
| chr19:1636890
|
C | T | 4 | a0001c0005t0009g0016a0001c0005t0023g0015a0001c0005t0038g0025others(1): Show | 4 | NA18962.hp2 NA18990.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-4485G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636890 | ||||||
| chr19:1636926
|
G | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-4521C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636926 | ||||||
| chr19:1636961
|
G | T | 3 | a0002c0001t0006g0063a0002c0001t0007g0064a0002c0001t0034g0309 | 3 | NA19066.hp2 NA19077.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.146-4556C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1636961 | ||||||
| chr19:1637003
|
A | T | 1 | a0001c0005t0004g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.146-4598T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637003 | ||||||
| chr19:1637022
|
G | A | 1 | a0001c0003t0009g0007 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.146-4617C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637022 | ||||||
| chr19:1637039
|
T | G | 1 | a0001c0005t0030g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.146-4634A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637039 | ||||||
| chr19:1637053
|
C | T | 1 | a0002c0001t0007g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.146-4648G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637053 | ||||||
| chr19:1637182
|
C | A | 1 | a0001c0005t0004g0027 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.146-4777G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637182 | ||||||
| chr19:1637203
|
CGCAACCT others(25): Show |
C | 65 | a0001c0002t0085g0304a0001c0005t0002g0224a0001c0005t0017g0293others(62): Show | 65 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.146-4830_146-4799d others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637203 | ||||||
| chr19:1637235
|
G | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-4830C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637235 | ||||||
| chr19:1637262
|
CGCCTGGC others(25): Show |
C | 3 | a0001c0002t0001g0180a0001c0002t0035g0349a0001c0002t0058g0283 | 3 | HG02055.hp2 HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.146-4889_146-4858d others(34): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637262 | ||||||
| chr19:1637510
|
C | A | 1 | a0002c0001t0006g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.146-5105G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637510 | ||||||
| chr19:1637632
|
G | A | 1 | a0001c0002t0002g0186 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.146-5227C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637632 | ||||||
| chr19:1637635
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-5230G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637635 | ||||||
| chr19:1637775
|
G | C | 1 | a0001c0002t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.146-5370C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637775 | ||||||
| chr19:1637904
|
A | G | 1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146-5499T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637904 | ||||||
| chr19:1637905
|
C | T | 1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146-5500G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637905 | ||||||
| chr19:1637913
|
A | G | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-5508T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637913 | ||||||
| chr19:1637919
|
G | A | 1 | a0001c0005t0097g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.146-5514C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637919 | ||||||
| chr19:1637920
|
A | G | 1 | a0001c0005t0097g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.146-5515T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637920 | ||||||
| chr19:1637925
|
G | A | 1 | a0001c0005t0097g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.146-5520C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637925 | ||||||
| chr19:1637966
|
G | C | 1 | a0001c0002t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.146-5561C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637966 | ||||||
| chr19:1637993
|
A | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-5588T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1637993 | ||||||
| chr19:1638072
|
T | A | 2 | a0001c0003t0001g0236a0001c0003t0002g0225 | 2 | HG06807.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.146-5667A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638072 | ||||||
| chr19:1638074
|
G | T | 3 | a0001c0004t0003g0220a0001c0004t0003g0279a0001c0004t0021g0321 | 3 | HG01243.hp2 HG02148.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.146-5669C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638074 | ||||||
| chr19:1638245
|
G | A | 1 | a0001c0004t0099g0343 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.146-5840C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638245 | ||||||
| chr19:1638491
|
A | G | 194 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(191): Show | 194 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.146-6086T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638491 | ||||||
| chr19:1638655
|
TGA | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-6252_146-6251d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638655 | ||||||
| chr19:1638663
|
C | T | 2 | a0001c0013t0037g0009a0001c0013t0042g0033 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.146-6258G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638663 | ||||||
| chr19:1638821
|
G | A | 1 | a0001c0004t0008g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.146-6416C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638821 | ||||||
| chr19:1638920
|
C | T | 131 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(128): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.146-6515G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638920 | ||||||
| chr19:1638934
|
G | C | 62 | a0001c0005t0002g0224a0001c0005t0017g0293a0001c0007t0001g0217others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.146-6529C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638934 | ||||||
| chr19:1638988
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-6583G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1638988 | ||||||
| chr19:1639022
|
T | C | 1 | a0003c0006t0002g0150 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.146-6617A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639022 | ||||||
| chr19:1639072
|
C | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.146-6667G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639072 | ||||||
| chr19:1639168
|
C | G | 3 | a0001c0003t0001g0096a0001c0003t0002g0094a0001c0003t0002g0095 | 3 | HG00741.hp1 HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.146-6763G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639168 | ||||||
| chr19:1639169
|
G | A | 1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.146-6764C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639169 | ||||||
| chr19:1639254
|
G | A | 86 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.146-6849C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639254 | ||||||
| chr19:1639296
|
G | A | 1 | a0002c0001t0007g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.146-6891C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639296 | ||||||
| chr19:1639304
|
A | G | 3 | a0001c0007t0074g0090a0001c0007t0096g0311a0002c0001t0100g0342 | 3 | HG03490.hp1 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.146-6899T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639304 | ||||||
| chr19:1639353
|
A | T | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-6948T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639353 | ||||||
| chr19:1639381
|
C | T | 1 | a0003c0006t0010g0141 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.145+6974G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639381 | ||||||
| chr19:1639472
|
G | A | 2 | a0001c0002t0002g0222a0001c0002t0005g0322 | 2 | NA19064.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.145+6883C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639472 | ||||||
| chr19:1639658
|
G | A | 1 | a0002c0001t0095g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.145+6697C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639658 | ||||||
| chr19:1639685
|
C | G | 62 | a0001c0005t0002g0224a0001c0005t0017g0293a0001c0007t0001g0217others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.145+6670G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639685 | ||||||
| chr19:1639751
|
G | GA | 116 | a0001c0002t0001g0078a0001c0002t0001g0138a0001c0002t0001g0209others(113): Show | 116 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.145+6603dupT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639751 | ||||||
| chr19:1639751
|
G | GAA | 24 | a0001c0002t0032g0161a0001c0003t0001g0096a0001c0003t0002g0094others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.145+6602_145+6603d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639751 | ||||||
| chr19:1639751
|
GA | G | 8 | a0001c0002t0001g0180a0001c0002t0027g0196a0001c0002t0058g0283others(5): Show | 8 | HG01943.hp2 HG02273.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.145+6603delT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639751 | ||||||
| chr19:1639944
|
C | T | 6 | a0001c0004t0003g0044a0001c0004t0003g0047a0001c0004t0062g0046others(3): Show | 6 | HG00609.hp2 HG01978.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+6411G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1639944 | ||||||
| chr19:1640018
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+6337G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640018 | ||||||
| chr19:1640069
|
T | G | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+6286A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640069 | ||||||
| chr19:1640080
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.145+6275C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640080 | ||||||
| chr19:1640132
|
G | A | 1 | a0002c0001t0006g0086 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.145+6223C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640132 | ||||||
| chr19:1640208
|
G | A | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.145+6147C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640208 | ||||||
| chr19:1640257
|
C | T | 1 | a0002c0001t0022g0318 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.145+6098G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640257 | ||||||
| chr19:1640306
|
C | A | 63 | a0001c0005t0002g0224a0001c0005t0017g0293a0001c0007t0001g0217others(60): Show | 63 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.145+6049G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640306 | ||||||
| chr19:1640315
|
C | T | 1 | a0001c0005t0009g0013 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.145+6040G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640315 | ||||||
| chr19:1640395
|
T | C | 3 | a0001c0007t0002g0282a0001c0007t0020g0289a0003c0011t0030g0139 | 3 | HG01891.hp2 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.145+5960A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640395 | ||||||
| chr19:1640410
|
C | CT | 63 | a0001c0005t0002g0224a0001c0005t0017g0293a0001c0007t0001g0217others(60): Show | 63 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.145+5944dupA | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640410 | ||||||
| chr19:1640536
|
C | G | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+5819G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640536 | ||||||
| chr19:1640553
|
T | A | 1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+5802A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640553 | ||||||
| chr19:1640557
|
A | G | 1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+5798T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640557 | ||||||
| chr19:1640577
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+5778C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640577 | ||||||
| chr19:1640761
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.145+5594C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640761 | ||||||
| chr19:1640803
|
C | CA | 7 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0003t0008g0098others(4): Show | 7 | HG00280.hp2 HG02055.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.145+5551dupT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640803 | ||||||
| chr19:1640828
|
A | C | 2 | a0002c0001t0006g0074a0002c0001t0006g0086 | 2 | HG00558.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.145+5527T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640828 | ||||||
| chr19:1640875
|
G | A | 9 | a0001c0003t0001g0255a0001c0003t0002g0242a0001c0003t0002g0243others(6): Show | 9 | HG01192.hp2 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+5480C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1640875 | ||||||
| chr19:1641034
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+5321G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641034 | ||||||
| chr19:1641162
|
C | CA | 286 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(283): Show | 287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.145+5192dupT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641162 | ||||||
| chr19:1641162
|
C | CAA | 8 | a0001c0002t0002g0272a0001c0005t0004g0031a0002c0001t0019g0084others(5): Show | 8 | HG01109.hp2 HG01884.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.145+5191_145+5192d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641162 | ||||||
| chr19:1641263
|
A | G | 1 | a0001c0002t0001g0218 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.145+5092T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641263 | ||||||
| chr19:1641297
|
G | A | 62 | a0001c0005t0002g0224a0001c0005t0017g0293a0001c0007t0001g0217others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.145+5058C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641297 | ||||||
| chr19:1641309
|
C | A | 1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+5046G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641309 | ||||||
| chr19:1641642
|
G | A | 86 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.145+4713C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641642 | ||||||
| chr19:1641702
|
C | A | 44 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(41): Show | 44 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.145+4653G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641702 | ||||||
| chr19:1641802
|
A | T | 1 | a0015c0024t0072g0179 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.145+4553T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641802 | ||||||
| chr19:1641841
|
T | C | 44 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(41): Show | 44 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.145+4514A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641841 | ||||||
| chr19:1641899
|
A | C | 41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.145+4456T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641899 | ||||||
| chr19:1641923
|
T | G | 63 | a0001c0005t0002g0224a0001c0005t0017g0293a0001c0007t0001g0217others(60): Show | 63 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.145+4432A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1641923 | ||||||
| chr19:1642119
|
T | C | 1 | a0021c0015t0001g0231 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.145+4236A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642119 | ||||||
| chr19:1642129
|
T | TAC | 14 | a0001c0002t0001g0111a0001c0002t0002g0175a0001c0002t0075g0185others(11): Show | 14 | HG00408.hp2 HG01358.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.145+4224_145+4225d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
T | TACAC | 16 | a0001c0002t0001g0181a0001c0005t0017g0293a0001c0007t0103g0351others(13): Show | 16 | HG00621.hp1 HG00673.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+4222_145+4225d others(6): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
T | TACACAC | 12 | a0001c0007t0001g0217a0002c0001t0006g0074a0002c0001t0006g0075others(9): Show | 12 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.145+4220_145+4225d others(8): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
TAC | T | 132 | a0001c0002t0001g0173a0001c0002t0002g0186a0001c0002t0002g0202others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.145+4224_145+4225d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
TACAC | T | 54 | a0001c0002t0005g0319a0001c0002t0065g0176a0001c0002t0093g0341others(51): Show | 55 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.145+4222_145+4225d others(6): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
TACACAC | T | 12 | a0001c0002t0001g0271a0001c0002t0002g0048a0001c0002t0002g0270others(9): Show | 12 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.145+4220_145+4225d others(8): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
TACACACA others(1): Show |
T | 48 | a0001c0002t0001g0078a0001c0002t0001g0198a0001c0002t0001g0209others(45): Show | 48 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.145+4218_145+4225d others(10): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
TACACACA others(5): Show |
T | 2 | a0001c0003t0002g0245a0001c0007t0002g0049 | 2 | HG01943.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.145+4214_145+4225d others(14): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642129
|
TACACACA others(7): Show |
T | 2 | a0001c0004t0003g0104a0001c0004t0003g0280 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.145+4212_145+4225d others(16): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642129 | ||||||
| chr19:1642157
|
C | CAG | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4197_145+4198i others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642157 | ||||||
| chr19:1642157
|
C | G | 41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.145+4198G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642157 | ||||||
| chr19:1642185
|
C | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4170G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642185 | ||||||
| chr19:1642186
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4169C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642186 | ||||||
| chr19:1642186
|
GCAGA | G | 3 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0002t0078g0189 | 3 | HG02886.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.145+4165_145+4168d others(6): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642186 | ||||||
| chr19:1642189
|
G | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4166C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642189 | ||||||
| chr19:1642190
|
A | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4165T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642190 | ||||||
| chr19:1642192
|
ACAGACG | A | 41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.145+4157_145+4162d others(8): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642192 | ||||||
| chr19:1642195
|
G | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4160C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642195 | ||||||
| chr19:1642200
|
A | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4155T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642200 | ||||||
| chr19:1642201
|
G | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4154C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642201 | ||||||
| chr19:1642203
|
C | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4152G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642203 | ||||||
| chr19:1642208
|
A | G | 3 | a0001c0002t0001g0180a0001c0002t0035g0349a0001c0002t0058g0283 | 3 | HG02055.hp2 HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.145+4147T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642208 | ||||||
| chr19:1642210
|
A | AGACACG | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4144_145+4145i others(8): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642210 | ||||||
| chr19:1642216
|
G | A | 3 | a0001c0002t0001g0180a0001c0002t0035g0349a0001c0002t0058g0283 | 3 | HG02055.hp2 HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.145+4139C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642216 | ||||||
| chr19:1642222
|
G | A | 62 | a0001c0005t0002g0224a0001c0005t0017g0293a0001c0007t0001g0217others(59): Show | 62 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.145+4133C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642222 | ||||||
| chr19:1642222
|
GCA | G | 4 | a0001c0007t0002g0282a0001c0007t0020g0289a0001c0007t0091g0300others(1): Show | 4 | HG01891.hp2 HG02615.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+4131_145+4132d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642222 | ||||||
| chr19:1642227
|
G | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4128C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642227 | ||||||
| chr19:1642233
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4122G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642233 | ||||||
| chr19:1642234
|
A | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4121T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642234 | ||||||
| chr19:1642238
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4117C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642238 | ||||||
| chr19:1642241
|
G | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4114C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642241 | ||||||
| chr19:1642248
|
A | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4107T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642248 | ||||||
| chr19:1642254
|
G | A | 2 | a0001c0003t0077g0241a0001c0004t0008g0151 | 2 | HG01074.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.145+4101C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642254 | ||||||
| chr19:1642255
|
T | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4100A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642255 | ||||||
| chr19:1642256
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+4099C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642256 | ||||||
| chr19:1642256
|
G | GCGCACAC others(5): Show |
41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.145+4087_145+4098d others(14): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642256 | ||||||
| chr19:1642269
|
C | T | 1 | a0001c0003t0002g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.145+4086G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642269 | ||||||
| chr19:1642271
|
C | G | 1 | a0001c0005t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.145+4084G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642271 | ||||||
| chr19:1642276
|
G | A | 1 | a0001c0005t0097g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.145+4079C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642276 | ||||||
| chr19:1642276
|
GCA | G | 3 | a0001c0005t0001g0207a0001c0005t0001g0208a0001c0005t0002g0131 | 3 | NA18986.hp1 NA19030.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.145+4077_145+4078d others(4): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642276 | ||||||
| chr19:1642278
|
A | G | 1 | a0001c0005t0097g0320 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.145+4077T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642278 | ||||||
| chr19:1642292
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.145+4063C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642292 | ||||||
| chr19:1642366
|
T | C | 1 | a0001c0005t0038g0025 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.145+3989A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642366 | ||||||
| chr19:1642459
|
A | G | 1 | a0003c0006t0012g0313 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.145+3896T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642459 | ||||||
| chr19:1642508
|
T | C | 41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.145+3847A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642508 | ||||||
| chr19:1642723
|
T | C | 28 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(25): Show | 28 | HG00621.hp2 HG01081.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.145+3632A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642723 | ||||||
| chr19:1642782
|
C | T | 79 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(76): Show | 79 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(76): Show |
intron_variant | MODIFIER | c.145+3573G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642782 | ||||||
| chr19:1642856
|
C | T | 9 | a0001c0003t0001g0255a0001c0003t0002g0242a0001c0003t0002g0243others(6): Show | 9 | HG01192.hp2 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+3499G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642856 | ||||||
| chr19:1642886
|
G | A | 1 | a0001c0004t0062g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.145+3469C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642886 | ||||||
| chr19:1642900
|
T | A | 41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.145+3455A>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642900 | ||||||
| chr19:1642910
|
T | C | 1 | a0001c0005t0023g0032 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.145+3445A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642910 | ||||||
| chr19:1642928
|
G | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+3427C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642928 | ||||||
| chr19:1642951
|
G | A | 1 | a0002c0001t0084g0290 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.145+3404C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1642951 | ||||||
| chr19:1643000
|
G | A | 41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.145+3355C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643000 | ||||||
| chr19:1643089
|
G | A | 1 | a0001c0007t0020g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.145+3266C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643089 | ||||||
| chr19:1643340
|
C | T | 5 | a0002c0001t0014g0058a0002c0001t0014g0059a0002c0001t0053g0057others(2): Show | 5 | HG02523.hp2 NA18948.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+3015G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643340 | ||||||
| chr19:1643346
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+3009C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643346 | ||||||
| chr19:1643411
|
A | G | 254 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(251): Show | 254 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.145+2944T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643411 | ||||||
| chr19:1643438
|
C | T | 1 | a0017c0026t0002g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.145+2917G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643438 | ||||||
| chr19:1643487
|
C | T | 1 | a0001c0002t0058g0283 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.145+2868G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643487 | ||||||
| chr19:1643539
|
T | C | 3 | a0001c0003t0001g0255a0001c0003t0002g0242a0001c0003t0002g0243 | 3 | HG02280.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.145+2816A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643539 | ||||||
| chr19:1643738
|
G | C | 16 | a0001c0002t0001g0180a0001c0002t0002g0190a0001c0002t0002g0191others(13): Show | 16 | HG02055.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.145+2617C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643738 | ||||||
| chr19:1643922
|
T | G | 279 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(276): Show | 279 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.145+2433A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643922 | ||||||
| chr19:1643942
|
T | C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+2413A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643942 | ||||||
| chr19:1643967
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+2388C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1643967 | ||||||
| chr19:1644127
|
C | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+2228G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644127 | ||||||
| chr19:1644158
|
C | T | 11 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0002t0013g0182others(8): Show | 11 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.145+2197G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644158 | ||||||
| chr19:1644289
|
G | C | 3 | a0001c0004t0003g0220a0001c0004t0003g0279a0001c0004t0021g0321 | 3 | HG01243.hp2 HG02148.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.145+2066C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644289 | ||||||
| chr19:1644391
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+1964G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644391 | ||||||
| chr19:1644396
|
AG | A | 83 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+1958delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644396 | ||||||
| chr19:1644437
|
G | T | 1 | a0001c0005t0027g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.145+1918C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644437 | ||||||
| chr19:1644459
|
C | T | 1 | a0001c0003t0060g0273 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.145+1896G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644459 | ||||||
| chr19:1644538
|
C | T | 24 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(21): Show | 24 | HG00621.hp2 HG01081.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.145+1817G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644538 | ||||||
| chr19:1644567
|
C | T | 19 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0178others(16): Show | 19 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.145+1788G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644567 | ||||||
| chr19:1644611
|
T | C | 3 | a0001c0004t0001g0166a0001c0004t0002g0257a0001c0004t0086g0303 | 3 | HG01361.hp2 HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.145+1744A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644611 | ||||||
| chr19:1644616
|
C | G | 3 | a0001c0003t0001g0096a0001c0003t0002g0094a0001c0003t0002g0095 | 3 | HG00741.hp1 HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.145+1739G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644616 | ||||||
| chr19:1644656
|
G | A | 41 | a0001c0003t0059g0187a0001c0004t0008g0151a0001c0005t0010g0117others(38): Show | 41 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.145+1699C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644656 | ||||||
| chr19:1644700
|
G | A | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.145+1655C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644700 | ||||||
| chr19:1644777
|
G | C | 1 | a0001c0007t0071g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+1578C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644777 | ||||||
| chr19:1644860
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+1495C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1644860 | ||||||
| chr19:1645004
|
C | T | 1 | a0002c0001t0019g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.145+1351G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645004 | ||||||
| chr19:1645149
|
C | T | 20 | a0001c0003t0001g0096a0001c0003t0002g0094a0001c0003t0002g0095others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.145+1206G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645149 | ||||||
| chr19:1645196
|
G | C | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.145+1159C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645196 | ||||||
| chr19:1645246
|
A | C | 1 | a0001c0002t0004g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.145+1109T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645246 | ||||||
| chr19:1645297
|
G | A | 31 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(28): Show | 31 | HG00621.hp2 HG01081.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.145+1058C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645297 | ||||||
| chr19:1645315
|
C | T | 1 | a0001c0007t0002g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.145+1040G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645315 | ||||||
| chr19:1645335
|
G | A | 1 | a0001c0005t0026g0037 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.145+1020C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645335 | ||||||
| chr19:1645343
|
C | A | 11 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0002t0013g0182others(8): Show | 11 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.145+1012G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645343 | ||||||
| chr19:1645345
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+1010C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645345 | ||||||
| chr19:1645349
|
C | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+1006G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645349 | ||||||
| chr19:1645389
|
C | T | 10 | a0002c0001t0006g0055a0002c0001t0006g0089a0002c0001t0007g0054others(7): Show | 10 | HG01358.hp2 HG02004.hp1 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.145+966G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645389 | ||||||
| chr19:1645460
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.145+895G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645460 | ||||||
| chr19:1645470
|
G | A | 82 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.145+885C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645470 | ||||||
| chr19:1645487
|
CCGGCCGG others(21): Show |
C | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+840_145+867del others(28): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645487 | ||||||
| chr19:1645498
|
C | T | 3 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0002t0078g0189 | 3 | HG02886.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.145+857G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645498 | ||||||
| chr19:1645549
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+806G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645549 | ||||||
| chr19:1645595
|
G | A | 1 | a0001c0003t0002g0245 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.145+760C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645595 | ||||||
| chr19:1645630
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+725G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645630 | ||||||
| chr19:1645676
|
C | A | 14 | a0001c0003t0002g0247a0001c0004t0001g0166a0001c0004t0002g0257others(11): Show | 14 | HG00099.hp2 HG00735.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.145+679G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645676 | ||||||
| chr19:1645680
|
T | C | 44 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(41): Show | 44 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.145+675A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645680 | ||||||
| chr19:1645764
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+591C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645764 | ||||||
| chr19:1645770
|
C | T | 2 | a0001c0003t0005g0331a0001c0007t0001g0232 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.145+585G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645770 | ||||||
| chr19:1645794
|
G | A | 4 | a0001c0003t0076g0045a0001c0004t0003g0044a0001c0004t0003g0047others(1): Show | 4 | HG01978.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+561C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645794 | ||||||
| chr19:1645818
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+537G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645818 | ||||||
| chr19:1645819
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+536C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1645819 | ||||||
| chr19:1646080
|
A | T | 2 | a0001c0003t0001g0226a0001c0003t0001g0230 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.145+275T>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1646080 | ||||||
| chr19:1646098
|
C | G | 1 | a0002c0001t0007g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.145+257G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1646098 | ||||||
| chr19:1646119
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.145+236G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1646119 | ||||||
| chr19:1646178
|
G | A | 1 | a0001c0003t0002g0275 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.145+177C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1646178 | ||||||
| chr19:1646214
|
G | A | 29 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(26): Show | 29 | HG00621.hp2 HG01081.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.145+141C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1646214 | ||||||
| chr19:1646222
|
C | T | 111 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(108): Show | 111 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.145+133G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 3/18 | chr19 | 1646222 | ||||||
| chr19:1646527
|
G | A | 2 | a0001c0002t0001g0180a0001c0002t0058g0283 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.73-100C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646527 | ||||||
| chr19:1646599
|
A | C | 1 | a0001c0005t0004g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.73-172T>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646599 | ||||||
| chr19:1646605
|
C | T | 2 | a0001c0003t0002g0225a0003c0011t0063g0093 | 2 | HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.73-178G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646605 | ||||||
| chr19:1646606
|
G | A | 1 | a0004c0014t0013g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.73-179C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646606 | ||||||
| chr19:1646607
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-180G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646607 | ||||||
| chr19:1646651
|
T | G | 1 | a0001c0002t0002g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.73-224A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646651 | ||||||
| chr19:1646666
|
C | G | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.73-239G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646666 | ||||||
| chr19:1646703
|
G | A | 1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.73-276C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646703 | ||||||
| chr19:1646713
|
C | T | 41 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.73-286G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646713 | ||||||
| chr19:1646761
|
G | A | 3 | a0001c0004t0003g0220a0001c0004t0003g0279a0001c0004t0021g0321 | 3 | HG01243.hp2 HG02148.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.73-334C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646761 | ||||||
| chr19:1646810
|
G | A | 3 | a0001c0002t0035g0349a0001c0003t0001g0200a0001c0003t0001g0201 | 3 | HG02055.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.73-383C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646810 | ||||||
| chr19:1646830
|
G | A | 1 | a0001c0005t0004g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.73-403C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646830 | ||||||
| chr19:1646905
|
G | C | 1 | a0001c0003t0002g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.73-478C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646905 | ||||||
| chr19:1646914
|
G | A | 13 | a0001c0002t0002g0190a0001c0002t0002g0191a0001c0002t0013g0182others(10): Show | 13 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-487C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646914 | ||||||
| chr19:1646954
|
CG | C | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-528delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646954 | ||||||
| chr19:1646995
|
G | A | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-568C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1646995 | ||||||
| chr19:1647041
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.73-614C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647041 | ||||||
| chr19:1647118
|
G | C | 1 | a0002c0001t0014g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.73-691C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647118 | ||||||
| chr19:1647229
|
C | A | 1 | a0003c0006t0067g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.73-802G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647229 | ||||||
| chr19:1647256
|
T | C | 2 | a0001c0007t0103g0351a0010c0023t0051g0140 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.73-829A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647256 | ||||||
| chr19:1647326
|
G | A | 4 | a0001c0002t0001g0178a0001c0002t0001g0198a0001c0002t0002g0267others(1): Show | 4 | HG01192.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-899C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647326 | ||||||
| chr19:1647439
|
C | T | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.73-1012G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647439 | ||||||
| chr19:1647483
|
C | G | 1 | a0001c0002t0013g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.73-1056G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647483 | ||||||
| chr19:1647518
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.73-1091C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647518 | ||||||
| chr19:1647534
|
C | G | 1 | a0003c0006t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.73-1107G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647534 | ||||||
| chr19:1647591
|
C | T | 1 | a0001c0002t0002g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-1164G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647591 | ||||||
| chr19:1647622
|
C | T | 1 | a0001c0005t0045g0040 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.73-1195G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647622 | ||||||
| chr19:1647628
|
A | G | 235 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(232): Show | 235 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.73-1201T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647628 | ||||||
| chr19:1647696
|
G | A | 2 | a0001c0007t0071g0199a0015c0024t0072g0179 | 2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.73-1269C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647696 | ||||||
| chr19:1647951
|
C | T | 2 | a0001c0005t0004g0011a0001c0005t0004g0027 | 2 | HG04115.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.73-1524G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647951 | ||||||
| chr19:1647952
|
G | C | 2 | a0001c0003t0001g0200a0001c0003t0001g0201 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.73-1525C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1647952 | ||||||
| chr19:1648153
|
C | T | 1 | a0001c0004t0003g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.73-1726G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648153 | ||||||
| chr19:1648162
|
T | C | 2 | a0001c0013t0037g0009a0001c0013t0042g0033 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.73-1735A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648162 | ||||||
| chr19:1648215
|
C | T | 3 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170 | 3 | HG01109.hp2 HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73-1788G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648215 | ||||||
| chr19:1648261
|
G | A | 6 | a0002c0001t0015g0080a0002c0001t0015g0081a0002c0001t0015g0088others(3): Show | 6 | HG01358.hp2 HG02004.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-1834C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648261 | ||||||
| chr19:1648339
|
C | T | 1 | a0002c0001t0022g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.72+1838G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648339 | ||||||
| chr19:1648660
|
G | T | 1 | a0001c0002t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.72+1517C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648660 | ||||||
| chr19:1648670
|
T | C | 1 | a0002c0001t0088g0292 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.72+1507A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648670 | ||||||
| chr19:1648817
|
T | TG | 28 | a0001c0002t0001g0203a0001c0002t0002g0202a0001c0002t0035g0349others(25): Show | 28 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.72+1359dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648817 | ||||||
| chr19:1648817
|
TG | T | 158 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(155): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.72+1359delC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648817 | ||||||
| chr19:1648817
|
TGGG | T | 38 | a0001c0002t0004g0012a0001c0002t0041g0004a0001c0002t0046g0039others(35): Show | 38 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.72+1357_72+1359del others(3): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648817 | ||||||
| chr19:1648821
|
G | T | 1 | a0001c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.72+1356C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648821 | ||||||
| chr19:1648823
|
G | T | 1 | a0001c0002t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72+1354C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648823 | ||||||
| chr19:1648827
|
G | C | 6 | a0001c0003t0002g0258a0001c0003t0005g0338a0001c0007t0002g0259others(3): Show | 6 | HG00423.hp1 HG02129.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+1350C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648827 | ||||||
| chr19:1648827
|
G | T | 79 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.72+1350C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648827 | ||||||
| chr19:1648829
|
G | T | 2 | a0001c0002t0005g0319a0001c0004t0066g0172 | 2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.72+1348C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648829 | ||||||
| chr19:1648947
|
G | A | 2 | a0001c0002t0002g0222a0001c0002t0005g0322 | 2 | NA19064.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.72+1230C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648947 | ||||||
| chr19:1648970
|
G | A | 1 | a0002c0001t0006g0089 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.72+1207C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648970 | ||||||
| chr19:1648988
|
C | A | 3 | a0001c0007t0074g0090a0001c0007t0096g0311a0002c0001t0100g0342 | 3 | HG03490.hp1 HG03492.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.72+1189G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1648988 | ||||||
| chr19:1649124
|
C | T | 8 | a0001c0007t0002g0049a0002c0001t0016g0050a0002c0001t0016g0051others(5): Show | 8 | HG00642.hp2 HG01070.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+1053G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649124 | ||||||
| chr19:1649258
|
G | A | 3 | a0001c0003t0001g0261a0001c0003t0005g0336a0007c0016t0002g0260 | 3 | HG01952.hp1 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.72+919C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649258 | ||||||
| chr19:1649323
|
C | T | 10 | a0001c0003t0001g0152a0001c0003t0001g0226a0001c0003t0001g0227others(7): Show | 11 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+854G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649323 | ||||||
| chr19:1649326
|
A | G | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+851T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649326 | ||||||
| chr19:1649364
|
T | C | 146 | a0001c0002t0001g0078a0001c0002t0001g0209a0001c0002t0001g0212others(143): Show | 146 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.72+813A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649364 | ||||||
| chr19:1649394
|
G | A | 7 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305others(4): Show | 7 | HG01106.hp2 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+783C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649394 | ||||||
| chr19:1649424
|
CTTT | C | 79 | a0001c0002t0001g0111a0001c0002t0001g0132a0001c0002t0001g0138others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.72+750_72+752delAA others(1): Show |
TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649424 | ||||||
| chr19:1649586
|
G | A | 1 | a0001c0005t0002g0224 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.72+591C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649586 | ||||||
| chr19:1649879
|
G | T | 1 | a0001c0003t0002g0225 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.72+298C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649879 | ||||||
| chr19:1649902
|
C | A | 1 | a0001c0005t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.72+275G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649902 | ||||||
| chr19:1649969
|
C | T | 4 | a0004c0033t0036g0350a0005c0010t0018g0169a0005c0010t0018g0170others(1): Show | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+208G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649969 | ||||||
| chr19:1649970
|
G | A | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.72+207C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649970 | ||||||
| chr19:1649973
|
C | T | 3 | a0001c0002t0085g0304a0004c0014t0013g0288a0004c0014t0079g0305 | 3 | HG01106.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.72+204G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1649973 | ||||||
| chr19:1650020
|
CAG | C | 4 | a0001c0002t0001g0132a0001c0002t0002g0133a0001c0002t0005g0330others(1): Show | 4 | HG02145.hp2 HG02257.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+155_72+156delCT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1650020 | ||||||
| chr19:1650135
|
A | G | 276 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(273): Show | 276 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.72+42T>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 2/18 | chr19 | 1650135 | ||||||
| chr19:1650320
|
G | A | 1 | a0001c0004t0094g0327 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-39-33C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1650320 | ||||||
| chr19:1650326
|
CAG | C | 3 | a0001c0003t0001g0261a0001c0003t0005g0336a0007c0016t0002g0260 | 3 | HG01952.hp1 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-39-41_-39-40delCT | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1650326 | ||||||
| chr19:1650351
|
G | A | 6 | a0001c0004t0003g0153a0001c0004t0011g0134a0001c0004t0011g0135others(3): Show | 6 | HG00741.hp2 HG01074.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39-64C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1650351 | ||||||
| chr19:1650578
|
G | A | 2 | a0006c0012t0020g0262a0006c0012t0020g0263 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-39-291C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1650578 | ||||||
| chr19:1650984
|
G | A | 2 | a0001c0002t0001g0265a0001c0002t0002g0264 | 2 | NA18970.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-39-697C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1650984 | ||||||
| chr19:1651102
|
T | G | 1 | a0001c0002t0001g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-39-815A>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651102 | ||||||
| chr19:1651226
|
C | T | 1 | a0001c0003t0005g0338 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-39-939G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651226 | ||||||
| chr19:1651245
|
C | T | 1 | a0001c0004t0001g0166 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-39-958G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651245 | ||||||
| chr19:1651435
|
G | A | 1 | a0001c0004t0002g0154 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-40+865C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651435 | ||||||
| chr19:1651449
|
C | G | 1 | a0001c0003t0005g0337 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-40+851G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651449 | ||||||
| chr19:1651517
|
G | A | 1 | a0002c0001t0095g0317 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-40+783C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651517 | ||||||
| chr19:1651519
|
T | TG | 15 | a0001c0002t0005g0328a0001c0003t0001g0281a0001c0003t0005g0340others(12): Show | 15 | HG01109.hp2 HG01175.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40+780dupC | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651519 | ||||||
| chr19:1651577
|
C | G | 2 | a0001c0003t0001g0165a0018c0018t0001g0164 | 2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-40+723G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651577 | ||||||
| chr19:1651601
|
G | A | 4 | a0001c0003t0076g0045a0001c0004t0003g0044a0001c0004t0003g0047others(1): Show | 4 | HG01978.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+699C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651601 | ||||||
| chr19:1651799
|
G | GC | 57 | a0001c0002t0001g0271a0001c0002t0002g0143a0001c0002t0002g0267others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.-40+500dupG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651799 | ||||||
| chr19:1651805
|
C | A | 5 | a0002c0001t0015g0155a0002c0001t0029g0156a0002c0001t0029g0159others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+495G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651805 | ||||||
| chr19:1651807
|
C | G | 1 | a0012c0030t0002g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-40+493G>C | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651807 | ||||||
| chr19:1651877
|
T | C | 1 | a0003c0006t0001g0160 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-40+423A>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651877 | ||||||
| chr19:1651904
|
G | A | 1 | a0001c0007t0020g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-40+396C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651904 | ||||||
| chr19:1651976
|
G | T | 1 | a0001c0029t0002g0162 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-40+324C>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1651976 | ||||||
| chr19:1652067
|
G | A | 1 | a0001c0004t0086g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-40+233C>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1652067 | ||||||
| chr19:1652089
|
C | A | 1 | a0001c0002t0032g0161 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-40+211G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1652089 | ||||||
| chr19:1652109
|
G | C | 1 | a0001c0007t0103g0351 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-40+191C>G | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1652109 | ||||||
| chr19:1652117
|
C | A | 29 | a0001c0002t0004g0012a0001c0005t0004g0011a0001c0005t0004g0017others(26): Show | 29 | HG01123.hp1 HG01167.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.-40+183G>T | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1652117 | ||||||
| chr19:1652162
|
C | T | 4 | a0001c0003t0076g0045a0001c0004t0003g0044a0001c0004t0003g0047others(1): Show | 4 | HG01978.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40+138G>A | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1652162 | ||||||
| chr19:1652204
|
G | GC | 17 | a0001c0002t0058g0283a0001c0002t0083g0307a0001c0002t0085g0304others(14): Show | 17 | HG01106.hp2 HG01175.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-40+95dupG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1652204 | ||||||
| chr19:1652204
|
GC | G | 178 | a0001c0002t0001g0078a0001c0002t0001g0111a0001c0002t0001g0132others(175): Show | 178 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-40+95delG | TCF3 | ENSG00000071564.19 | transcript | ENST00000262965.12 | protein_coding | 1/18 | chr19 | 1652204 |