| geneid | 6942 |
|---|---|
| ensemblid | ENSG00000100207.21 |
| hgncid | 11631 |
| symbol | TCF20 |
| name | transcription factor 20 |
| refseq_nuc | NM_001378418.1 |
| refseq_prot | NP_001365347.1 |
| ensembl_nuc | ENST00000677622.1 |
| ensembl_prot | ENSP00000503828.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 42160013 |
| end | 42270653 |
| strand | - |
| ver | v1.2 |
| region | chr22:42160013-42270653 |
| region5000 | chr22:42155013-42275653 |
| regionname0 | TCF20_chr22_42160013_42270653 |
| regionname5000 | TCF20_chr22_42155013_42275653 |
| 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 | 0/1 | 1960 | 232 | 53 | 47 | 97 | 11 | 23 | 82 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002 | 0/0 | 1960 | 67 | 7 | 12 | 40 | 5 | 3 | 30 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003 | 0/0 | 1960 | 26 | 9 | 11 | 1 | 0 | 5 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0004 | 0/0 | 1960 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0005 | 0/0 | 1960 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0006 | 0/0 | 1960 | 3 | 0 | 0 | 1 | 0 | 2 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0007 | 0/0 | 1960 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0008 | 0/0 | 1960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0009 | 0/0 | 1960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0010 | 0/0 | 1960 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0011 | 0/0 | 1960 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0012 | 0/0 | 1960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0013 | 0/0 | 1960 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0014 | 0/0 | 1960 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0015 | 0/0 | 1960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0016 | 0/0 | 1960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| 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 | 5883 | 132 | 32 | 28 | 57 | 4 | 11 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0002 | 0/1 | 5883 | 88 | 15 | 18 | 40 | 6 | 8 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0003 | 0/0 | 5883 | 62 | 3 | 12 | 39 | 5 | 3 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0004 | 0/0 | 5883 | 24 | 8 | 11 | 1 | 0 | 4 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0005 | 0/0 | 5883 | 13 | 13 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0006 | 0/0 | 5883 | 4 | 4 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0007 | 0/0 | 5883 | 4 | 4 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0008 | 0/0 | 5883 | 3 | 0 | 0 | 1 | 0 | 2 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0009 | 0/0 | 5883 | 3 | 3 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0010 | 0/0 | 5883 | 2 | 1 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0011 | 0/0 | 5883 | 2 | 2 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0012 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0013 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0014 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0015 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0016 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0017 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0018 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0019 | 0/0 | 5883 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0020 | 0/0 | 5883 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0021 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0022 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0023 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0024 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0025 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0026 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0027 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0028 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| c0029 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| 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 | 0/1 | 1742 | 284 | 38 | 66 | 131 | 14 | 34 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0002 | 0/0 | 1743 | 34 | 29 | 2 | 2 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0003 | 0/0 | 1743 | 10 | 10 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0004 | 0/0 | 1742 | 4 | 3 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0005 | 0/0 | 1742 | 3 | 0 | 0 | 3 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0006 | 0/0 | 1748 | 2 | 1 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0007 | 0/0 | 1742 | 2 | 2 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0008 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0009 | 0/0 | 1747 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0010 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0011 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0012 | 0/0 | 1742 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0013 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0014 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0015 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0016 | 0/0 | 1742 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0017 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0018 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0019 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0020 | 0/0 | 1743 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0021 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| t0022 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 5883 | 132 | 32 | 28 | 57 | 4 | 11 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002 | 0/1 | 5883 | 88 | 15 | 18 | 40 | 6 | 8 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0006 | 0/0 | 5883 | 4 | 4 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0010 | 0/0 | 5883 | 2 | 1 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0012 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0016 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0017 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0021 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0022 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0028 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0003 | 0/0 | 5883 | 62 | 3 | 12 | 39 | 5 | 3 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0007 | 0/0 | 5883 | 4 | 4 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0023 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003c0004 | 0/0 | 5883 | 24 | 8 | 11 | 1 | 0 | 4 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003c0026 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003c0027 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0004c0005 | 0/0 | 5883 | 13 | 13 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0005c0009 | 0/0 | 5883 | 3 | 3 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0006c0008 | 0/0 | 5883 | 3 | 0 | 0 | 1 | 0 | 2 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0007c0011 | 0/0 | 5883 | 2 | 2 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0008c0024 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0009c0025 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0010c0014 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0011c0020 | 0/0 | 5883 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0012c0018 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0013c0015 | 0/0 | 5883 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0014c0019 | 0/0 | 5883 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0015c0013 | 0/0 | 5883 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0016c0029 | 0/0 | 5883 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7624 | 106 | 16 | 26 | 50 | 3 | 11 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0002 | 0/0 | 7625 | 10 | 8 | 1 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0003 | 0/0 | 7625 | 5 | 5 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0004 | 0/0 | 7624 | 2 | 1 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0005 | 0/0 | 7624 | 3 | 0 | 0 | 3 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0010 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0012 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0013 | 0/0 | 7634 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0015 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0016 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0001t0019 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0001 | 0/1 | 7624 | 76 | 10 | 15 | 37 | 5 | 8 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0002 | 0/0 | 7625 | 5 | 2 | 1 | 1 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0007 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0009 | 0/0 | 7629 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0011 | 0/0 | 7636 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0014 | 0/0 | 7625 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0018 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0002t0020 | 0/0 | 7625 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0006t0002 | 0/0 | 7625 | 4 | 4 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0010t0006 | 0/0 | 7630 | 2 | 1 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0012t0002 | 0/0 | 7625 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0016t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0017t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0021t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0022t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0001c0028t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0003t0001 | 0/0 | 7624 | 60 | 2 | 12 | 38 | 5 | 3 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0003t0017 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0003t0021 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0007t0001 | 0/0 | 7624 | 3 | 3 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0007t0003 | 0/0 | 7625 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0002c0023t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003c0004t0001 | 0/0 | 7624 | 20 | 4 | 11 | 1 | 0 | 4 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003c0004t0003 | 0/0 | 7625 | 4 | 4 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003c0026t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0003c0027t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0004c0005t0002 | 0/0 | 7625 | 13 | 13 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0005c0009t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0005c0009t0008 | 0/0 | 7625 | 2 | 2 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0006c0008t0001 | 0/0 | 7624 | 3 | 0 | 0 | 1 | 0 | 2 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0007c0011t0004 | 0/0 | 7624 | 2 | 2 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0008c0024t0001 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0009c0025t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0010c0014t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0011c0020t0001 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0012c0018t0002 | 0/0 | 7625 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0013c0015t0001 | 0/0 | 7624 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0014c0019t0001 | 0/0 | 7624 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0015c0013t0001 | 0/0 | 7624 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| a0016c0029t0022 | 0/0 | 7624 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | copy fasta | chr22 | 42155013 | 42275653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0012g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0015g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0016g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0001t0019g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0339 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0009g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0011g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0014g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0018g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0002t0020g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0006t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0006t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0006t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0006t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0010t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0010t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0012t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0016t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0017t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0021t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0022t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0001c0028t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0003t0021g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0007t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0007t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0007t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0007t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0002c0023t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0004t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0026t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0003c0027t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0004c0005t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0005c0009t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0005c0009t0008g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0005c0009t0008g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0006c0008t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0006c0008t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0006c0008t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0007c0011t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0007c0011t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0008c0024t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0009c0025t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0010c0014t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0011c0020t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0012c0018t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0013c0015t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0014c0019t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0015c0013t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| a0016c0029t0022g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0256 | EUR | GBR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0032 | EUR | GBR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0270 | EUR | FIN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0314 | EUR | FIN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0022 | EUR | FIN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00544 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00639 | hp1 | a0003 | c0004 | t0001 | g0107 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0342 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0069 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00733 | hp2 | a0003 | c0004 | t0001 | g0115 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0321 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00738 | hp1 | a0002 | c0003 | t0001 | g0055 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG00741 | hp2 | a0001 | c0002 | t0020 | g0286 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0034 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01070 | hp1 | a0003 | c0004 | t0001 | g0120 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0035 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01071 | hp2 | a0003 | c0004 | t0001 | g0119 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0053 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01081 | hp2 | a0011 | c0020 | t0001 | g0340 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01099 | hp1 | a0003 | c0004 | t0001 | g0105 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0313 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0052 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0128 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0117 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01175 | hp2 | a0003 | c0004 | t0001 | g0106 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0110 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01243 | hp2 | a0001 | c0010 | t0006 | g0008 | AMR | PUR | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0023 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0026 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01261 | hp1 | a0003 | c0004 | t0001 | g0104 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01346 | hp1 | a0003 | c0004 | t0001 | g0127 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0056 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0030 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0350 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | CLM | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0287 | EUR | IBS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0025 | EUR | IBS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01516 | hp1 | a0001 | c0001 | t0016 | g0147 | EUR | IBS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0259 | EUR | IBS | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0344 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01884 | hp2 | a0001 | c0006 | t0002 | g0247 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0322 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0054 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01978 | hp2 | a0001 | c0002 | t0009 | g0001 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01981 | hp1 | a0001 | c0001 | t0012 | g0205 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0338 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0288 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02004 | hp1 | a0014 | c0019 | t0001 | g0214 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0309 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02015 | hp1 | a0002 | c0003 | t0021 | g0087 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02055 | hp1 | a0012 | c0018 | t0002 | g0243 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02055 | hp2 | a0003 | c0004 | t0001 | g0108 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0049 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02071 | hp2 | a0001 | c0002 | t0014 | g0129 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02080 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02083 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02145 | hp1 | a0001 | c0010 | t0006 | g0009 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0308 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02258 | hp2 | a0001 | c0006 | t0002 | g0246 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02280 | hp2 | a0004 | c0005 | t0002 | g0235 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0341 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0310 | AMR | PEL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02451 | hp2 | a0004 | c0005 | t0002 | g0236 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0072 | EAS | KHV | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0112 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02572 | hp2 | a0005 | c0009 | t0008 | g0355 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02602 | hp1 | a0001 | c0022 | t0001 | g0162 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02622 | hp1 | a0004 | c0005 | t0002 | g0241 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02622 | hp2 | a0001 | c0002 | t0007 | g0103 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02630 | hp1 | a0001 | c0002 | t0007 | g0102 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02647 | hp1 | a0002 | c0007 | t0001 | g0078 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02647 | hp2 | a0004 | c0005 | t0002 | g0233 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02698 | hp1 | a0003 | c0004 | t0001 | g0351 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0033 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02717 | hp2 | a0003 | c0004 | t0001 | g0111 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02723 | hp1 | a0004 | c0005 | t0002 | g0234 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0328 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02809 | hp1 | a0003 | c0004 | t0003 | g0125 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02818 | hp1 | a0001 | c0006 | t0002 | g0250 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02886 | hp1 | a0008 | c0024 | t0001 | g0037 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02886 | hp2 | a0001 | c0006 | t0002 | g0249 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0074 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02897 | hp2 | a0001 | c0012 | t0002 | g0231 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02965 | hp1 | a0002 | c0007 | t0001 | g0085 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02976 | hp1 | a0004 | c0005 | t0002 | g0239 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0114 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0317 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03041 | hp1 | a0004 | c0005 | t0002 | g0229 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03098 | hp1 | a0003 | c0026 | t0001 | g0345 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03098 | hp2 | a0003 | c0004 | t0003 | g0126 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03139 | hp1 | a0004 | c0005 | t0002 | g0242 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03195 | hp1 | a0002 | c0007 | t0003 | g0084 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03195 | hp2 | a0003 | c0004 | t0001 | g0109 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0327 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03225 | hp2 | a0002 | c0003 | t0017 | g0066 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0132 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03490 | hp1 | a0003 | c0004 | t0001 | g0118 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03490 | hp2 | a0002 | c0003 | t0001 | g0018 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03491 | hp1 | a0003 | c0027 | t0001 | g0124 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0294 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03492 | hp1 | a0003 | c0004 | t0001 | g0123 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0295 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03516 | hp2 | a0004 | c0005 | t0002 | g0237 | AFR | ESN | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03540 | hp1 | a0004 | c0005 | t0002 | g0232 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0265 | AFR | GWD | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03579 | hp1 | a0007 | c0011 | t0004 | g0244 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03579 | hp2 | a0016 | c0029 | t0022 | g0354 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0306 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03704 | hp1 | a0006 | c0008 | t0001 | g0080 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03704 | hp2 | a0001 | c0021 | t0001 | g0200 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0029 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0330 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03927 | hp2 | a0001 | c0028 | t0001 | g0133 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03942 | hp2 | a0013 | c0015 | t0001 | g0312 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG04184 | hp1 | a0003 | c0004 | t0001 | g0113 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | BEB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG04199 | hp2 | a0001 | c0016 | t0001 | g0311 | SAS | STU | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG04228 | hp2 | a0006 | c0008 | t0001 | g0071 | SAS | STU | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18522 | hp1 | a0001 | c0001 | t0015 | g0337 | AFR | YRI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | CHB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18747 | hp2 | a0010 | c0014 | t0001 | g0352 | EAS | CHB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18906 | hp1 | a0004 | c0005 | t0002 | g0240 | AFR | YRI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18906 | hp2 | a0005 | c0009 | t0001 | g0089 | AFR | YRI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0050 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0062 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18962 | hp2 | a0003 | c0004 | t0001 | g0122 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18968 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18971 | hp2 | a0015 | c0013 | t0001 | g0059 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18977 | hp1 | a0009 | c0025 | t0001 | g0019 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18989 | hp2 | a0001 | c0001 | t0019 | g0187 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18995 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0335 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19009 | hp1 | a0001 | c0002 | t0011 | g0003 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19030 | hp1 | a0004 | c0005 | t0002 | g0230 | AFR | LWK | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19043 | hp2 | a0005 | c0009 | t0008 | g0353 | AFR | LWK | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19054 | hp2 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19065 | hp1 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19068 | hp1 | a0006 | c0008 | t0001 | g0028 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19068 | hp2 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0346 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0298 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19088 | hp2 | a0002 | c0023 | t0001 | g0057 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | YRI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA19240 | hp2 | a0004 | c0005 | t0002 | g0238 | AFR | YRI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA20752 | hp1 | a0001 | c0017 | t0001 | g0150 | EUR | TSI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0031 | EUR | TSI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0307 | EUR | TSI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA20805 | hp2 | a0002 | c0003 | t0001 | g0024 | EUR | TSI | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02109 | hp2 | a0001 | c0002 | t0018 | g0261 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02486 | hp1 | a0003 | c0004 | t0003 | g0347 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02486 | hp2 | a0007 | c0011 | t0004 | g0254 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0138 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0349 | AFR | ACB | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0326 | AFR | MSL | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG06807 | hp1 | a0002 | c0007 | t0001 | g0086 | AFR | USA | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | USA | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | USA | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | USA | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0079 | AFR | LWK | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| NA21309 | hp2 | a0003 | c0004 | t0003 | g0121 | AFR | LWK | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0339 | REF | REF | TCF20_chr22_42155013_42275653 | TCF20 | chr22 | 42155013 | 42275653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:42168711
|
G | A | 1 | a0009 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.5825C>T | p.Pro1942Leu | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/6 | 6176/7624 | 5825/5883 | 1942/1960 | chr22 | 42168711 | ||
| chr22:42168712
|
G | A | 1 | a0012 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.5824C>T | p.Pro1942Ser | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/6 | 6175/7624 | 5824/5883 | 1942/1960 | chr22 | 42168712 | ||
| chr22:42168712
|
G | T | 1 | a0013 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.5824C>A | p.Pro1942Thr | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/6 | 6175/7624 | 5824/5883 | 1942/1960 | chr22 | 42168712 | ||
| chr22:42209815
|
T | C | 1 | a0011 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.5491A>G | p.Thr1831Ala | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 5842/7624 | 5491/5883 | 1831/1960 | chr22 | 42209815 | ||
| chr22:42210106
|
G | A | 1 | a0014 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.5200C>T | p.Pro1734Ser | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 5551/7624 | 5200/5883 | 1734/1960 | chr22 | 42210106 | ||
| chr22:42210738
|
G | A | 1 | a0011 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.4568C>T | p.Pro1523Leu | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 4919/7624 | 4568/5883 | 1523/1960 | chr22 | 42210738 | ||
| chr22:42210985
|
C | T | 1 | a0010 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.4321G>A | p.Val1441Met | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 4672/7624 | 4321/5883 | 1441/1960 | chr22 | 42210985 | ||
| chr22:42211065
|
G | A | 1 | a0007 | 2 | HG02486.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.4241C>T | p.Ser1414Leu | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 4592/7624 | 4241/5883 | 1414/1960 | chr22 | 42211065 | ||
| chr22:42211332
|
C | T | 3 | a0005a0007a0016 | 6 | HG02486.hp2 HG02572.hp2 HG03579.hp1 others(3): Show |
missense_variant | MODERATE | c.3974G>A | p.Ser1325Asn | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 4325/7624 | 3974/5883 | 1325/1960 | chr22 | 42211332 | ||
| chr22:42211605
|
C | T | 1 | a0008 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.3701G>A | p.Ser1234Asn | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 4052/7624 | 3701/5883 | 1234/1960 | chr22 | 42211605 | ||
| chr22:42211811
|
C | T | 1 | a0004 | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
missense_variant | MODERATE | c.3495G>A | p.Met1165Ile | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 3846/7624 | 3495/5883 | 1165/1960 | chr22 | 42211811 | ||
| chr22:42213142
|
T | C | 5 | a0002a0006a0008others(2): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
missense_variant | MODERATE | c.2164A>G | p.Ser722Gly | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 2515/7624 | 2164/5883 | 722/1960 | chr22 | 42213142 | ||
| chr22:42214093
|
T | C | 1 | a0003 | 26 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(23): Show |
missense_variant | MODERATE | c.1213A>G | p.Met405Val | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 1564/7624 | 1213/5883 | 405/1960 | chr22 | 42214093 | ||
| chr22:42214722
|
G | T | 1 | a0015 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.584C>A | p.Pro195Gln | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 935/7624 | 584/5883 | 195/1960 | chr22 | 42214722 | ||
| chr22:42215109
|
G | A | 1 | a0016 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.197C>T | p.Ala66Val | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 548/7624 | 197/5883 | 66/1960 | chr22 | 42215109 | ||
| chr22:42215259
|
C | G | 1 | a0006 | 3 | HG03704.hp1 HG04228.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.47G>C | p.Ser16Thr | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 398/7624 | 47/5883 | 16/1960 | chr22 | 42215259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:42210251
|
C | T | 5 | a0001c0002a0001c0016a0003c0026others(2): Show | 92 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(89): Show |
synonymous_variant | LOW | c.5055G>A | p.Ser1685Ser | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 5406/7624 | 5055/5883 | 1685/1960 | chr22 | 42210251 | ||
| chr22:42210257
|
C | T | 1 | a0001c0017 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.5049G>A | p.Pro1683Pro | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 5400/7624 | 5049/5883 | 1683/1960 | chr22 | 42210257 | ||
| chr22:42210491
|
C | T | 2 | a0001c0016a0013c0015 | 2 | HG03942.hp2 HG04199.hp2 |
synonymous_variant | LOW | c.4815G>A | p.Val1605Val | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 5166/7624 | 4815/5883 | 1605/1960 | chr22 | 42210491 | ||
| chr22:42210899
|
T | C | 1 | a0003c0027 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.4407A>G | p.Ser1469Ser | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 4758/7624 | 4407/5883 | 1469/1960 | chr22 | 42210899 | ||
| chr22:42211493
|
T | C | 1 | a0001c0028 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.3813A>G | p.Gln1271Gln | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 4164/7624 | 3813/5883 | 1271/1960 | chr22 | 42211493 | ||
| chr22:42211883
|
A | G | 1 | a0001c0021 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.3423T>C | p.Asp1141Asp | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 3774/7624 | 3423/5883 | 1141/1960 | chr22 | 42211883 | ||
| chr22:42211931
|
C | T | 1 | a0002c0023 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.3375G>A | p.Gln1125Gln | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 3726/7624 | 3375/5883 | 1125/1960 | chr22 | 42211931 | ||
| chr22:42212645
|
G | A | 2 | a0001c0021a0001c0022 | 2 | HG02602.hp1 HG03704.hp2 |
synonymous_variant | LOW | c.2661C>T | p.His887His | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 3012/7624 | 2661/5883 | 887/1960 | chr22 | 42212645 | ||
| chr22:42213866
|
A | C | 1 | a0004c0005 | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
synonymous_variant | LOW | c.1440T>G | p.Thr480Thr | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 1791/7624 | 1440/5883 | 480/1960 | chr22 | 42213866 | ||
| chr22:42214250
|
A | G | 1 | a0001c0010 | 2 | HG01243.hp2 HG02145.hp1 |
synonymous_variant | LOW | c.1056T>C | p.Val352Val | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 1407/7624 | 1056/5883 | 352/1960 | chr22 | 42214250 | ||
| chr22:42214787
|
G | A | 1 | a0001c0028 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.519C>T | p.Ser173Ser | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 870/7624 | 519/5883 | 173/1960 | chr22 | 42214787 | ||
| chr22:42214865
|
G | A | 1 | a0002c0007 | 4 | HG02647.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.441C>T | p.Gly147Gly | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 792/7624 | 441/5883 | 147/1960 | chr22 | 42214865 | ||
| chr22:42214952
|
A | G | 1 | a0001c0012 | 1 | HG02897.hp2 | synonymous_variant | LOW | c.354T>C | p.Tyr118Tyr | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 705/7624 | 354/5883 | 118/1960 | chr22 | 42214952 | ||
| chr22:42215102
|
C | T | 1 | a0001c0006 | 4 | HG01884.hp2 HG02258.hp2 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.204G>A | p.Ala68Ala | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 555/7624 | 204/5883 | 68/1960 | chr22 | 42215102 | ||
| chr22:42215168
|
G | A | 1 | a0004c0005 | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
synonymous_variant | LOW | c.138C>T | p.Gly46Gly | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/6 | 489/7624 | 138/5883 | 46/1960 | chr22 | 42215168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:42160201
|
A | G | 1 | a0001c0002t0018 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1202T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 8452 | chr22 | 42160201 | |||||
| chr22:42160385
|
C | T | 1 | a0001c0002t0020 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 8268 | chr22 | 42160385 | |||||
| chr22:42160587
|
G | A | 1 | a0001c0001t0019 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*816C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 8066 | chr22 | 42160587 | |||||
| chr22:42160627
|
A | C | 1 | a0002c0003t0017 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 8026 | chr22 | 42160627 | |||||
| chr22:42160640
|
T | TA | 10 | a0001c0001t0002a0001c0002t0002a0001c0002t0014others(7): Show | 40 | HG00438.hp1 HG00741.hp2 HG01074.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*762dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 8012 | chr22 | 42160640 | |||||
| chr22:42160650
|
A | C | 1 | a0001c0001t0016 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*753T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 8003 | chr22 | 42160650 | |||||
| chr22:42160651
|
A | C | 1 | a0001c0001t0015 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*752T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 8002 | chr22 | 42160651 | |||||
| chr22:42160689
|
T | A | 2 | a0001c0001t0004a0007c0011t0004 | 4 | HG02486.hp2 HG02818.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*714A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7964 | chr22 | 42160689 | |||||
| chr22:42160865
|
C | T | 1 | a0001c0002t0014 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7788 | chr22 | 42160865 | |||||
| chr22:42160877
|
G | A | 1 | a0001c0001t0005 | 3 | NA18961.hp1 NA19010.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*526C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7776 | chr22 | 42160877 | |||||
| chr22:42160951
|
T | C | 1 | a0002c0003t0021 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7702 | chr22 | 42160951 | |||||
| chr22:42160981
|
T | TA | 3 | a0001c0001t0003a0002c0007t0003a0003c0004t0003 | 10 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*421dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7671 | chr22 | 42160981 | |||||
| chr22:42161247
|
T | G | 1 | a0001c0002t0007 | 2 | HG02622.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*156A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7406 | chr22 | 42161247 | |||||
| chr22:42161259
|
C | CGGGCG | 2 | a0001c0002t0009a0001c0010t0006 | 3 | HG01243.hp2 HG01978.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*139_*143dupCGCCC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7393 | chr22 | 42161259 | |||||
| chr22:42161259
|
C | CGGGCGGG others(3): Show |
1 | a0001c0001t0013 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134_*143dupCGCCCC others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7393 | chr22 | 42161259 | |||||
| chr22:42161323
|
C | T | 1 | a0001c0001t0012 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*80G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 6/6 | 7330 | chr22 | 42161323 | |||||
| chr22:42270422
|
C | CGGGGTGG others(5): Show |
1 | a0001c0002t0011 | 1 | NA19009.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132_-121dupCACCCC others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/6 | 55118 | chr22 | 42270422 | |||||
| chr22:42270423
|
G | A | 2 | a0005c0009t0008a0016c0029t0022 | 3 | HG02572.hp2 HG03579.hp2 NA19043.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-121C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/6 | chr22 | 42270423 | ||||||
| chr22:42270557
|
G | T | 1 | a0001c0001t0010 | 1 | NA18950.hp2 | 5_prime_UTR_variant | MODIFIER | c.-255C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/6 | 55252 | chr22 | 42270557 | |||||
| chr22:42270610
|
C | T | 1 | a0001c0002t0009 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-308G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/6 | 55305 | chr22 | 42270610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:42161470
|
G | A | 15 | a0001c0001t0001g0017a0001c0001t0003g0011a0001c0001t0003g0012others(12): Show | 15 | HG01891.hp1 HG02257.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.*45-112C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161470 | ||||||
| chr22:42161684
|
T | C | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.*45-326A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161684 | ||||||
| chr22:42161704
|
T | C | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.*45-346A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161704 | ||||||
| chr22:42161780
|
T | C | 4 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.*45-422A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161780 | ||||||
| chr22:42161972
|
C | CT | 36 | a0001c0001t0001g0135a0001c0001t0001g0251a0001c0001t0001g0293others(33): Show | 36 | HG00323.hp1 HG00639.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.*45-615dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTT | 56 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.*45-616_*45-615dup others(2): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTT | 39 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(36): Show | 39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.*45-617_*45-615dup others(3): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTT | 32 | a0001c0001t0001g0005a0001c0001t0001g0131a0001c0001t0001g0143others(29): Show | 32 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.*45-618_*45-615dup others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTT | 12 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(9): Show | 12 | HG01981.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.*45-619_*45-615dup others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0003g0011a0003c0004t0003g0121a0003c0004t0003g0125 | 3 | HG02809.hp1 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.*45-624_*45-615dup others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(4): Show |
2 | a0003c0004t0003g0126a0003c0004t0003g0347 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.*45-625_*45-615dup others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(5): Show |
1 | a0001c0006t0002g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*45-626_*45-615dup others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(6): Show |
2 | a0001c0006t0002g0247a0001c0006t0002g0249 | 2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.*45-627_*45-615dup others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(7): Show |
1 | a0012c0018t0002g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*45-628_*45-615dup others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(8): Show |
1 | a0001c0006t0002g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.*45-629_*45-615dup others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0002g0014 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*45-633_*45-615dup others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0350 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.*45-642_*45-615dup others(28): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
CTTTTTT | C | 7 | a0001c0001t0001g0253a0001c0001t0003g0012a0001c0001t0003g0013others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.*45-620_*45-615del others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
CTTTTTTT | C | 7 | a0001c0001t0001g0210a0001c0002t0002g0132a0001c0002t0002g0138others(4): Show | 7 | HG01952.hp1 HG02004.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.*45-621_*45-615del others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
CTTTTTTT others(8): Show |
C | 69 | a0001c0002t0001g0302a0002c0003t0001g0010a0002c0003t0001g0018others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.*45-629_*45-615del others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42161972
|
CTTTTTTT others(9): Show |
C | 2 | a0002c0003t0001g0023a0002c0003t0001g0041 | 2 | HG01256.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.*45-630_*45-615del others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42161972 | ||||||
| chr22:42162017
|
A | G | 1 | a0001c0002t0002g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*45-659T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42162017 | ||||||
| chr22:42162050
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.*45-692C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42162050 | ||||||
| chr22:42162169
|
T | A | 35 | a0001c0001t0001g0267a0001c0001t0002g0014a0001c0001t0002g0091others(32): Show | 35 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.*45-811A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42162169 | ||||||
| chr22:42162704
|
A | G | 10 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.*45-1346T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42162704 | ||||||
| chr22:42162934
|
CCA | C | 4 | a0001c0002t0001g0294a0001c0002t0001g0295a0001c0002t0001g0296others(1): Show | 4 | HG02602.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.*45-1578_*45-1577d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42162934 | ||||||
| chr22:42163045
|
G | A | 4 | a0001c0002t0001g0307a0001c0002t0001g0308a0001c0002t0001g0313others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.*45-1687C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163045 | ||||||
| chr22:42163070
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.*45-1712G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163070 | ||||||
| chr22:42163077
|
T | TGC | 3 | a0001c0001t0004g0095a0007c0011t0004g0244a0007c0011t0004g0254 | 3 | HG02486.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*45-1721_*45-1720d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163077 | ||||||
| chr22:42163109
|
G | A | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*45-1751C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163109 | ||||||
| chr22:42163289
|
G | A | 2 | a0003c0004t0001g0107a0003c0004t0001g0108 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.*45-1931C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163289 | ||||||
| chr22:42163352
|
C | G | 1 | a0013c0015t0001g0312 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.*45-1994G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163352 | ||||||
| chr22:42163820
|
G | A | 15 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0012t0002g0231others(12): Show | 15 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.*45-2462C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163820 | ||||||
| chr22:42163954
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*45-2596G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42163954 | ||||||
| chr22:42164157
|
C | T | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*45-2799G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164157 | ||||||
| chr22:42164161
|
G | A | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.*45-2803C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164161 | ||||||
| chr22:42164212
|
C | CTTTT | 14 | a0001c0001t0001g0267a0001c0001t0002g0344a0004c0005t0002g0229others(11): Show | 14 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.*45-2858_*45-2855d others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164212 | ||||||
| chr22:42164212
|
CT | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0099others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.*45-2855delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164212 | ||||||
| chr22:42164212
|
CTT | C | 210 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.*45-2856_*45-2855d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164212 | ||||||
| chr22:42164217
|
T | C | 1 | a0003c0004t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.*45-2859A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164217 | ||||||
| chr22:42164473
|
C | T | 1 | a0003c0004t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*45-3115G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164473 | ||||||
| chr22:42164486
|
G | A | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*45-3128C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164486 | ||||||
| chr22:42164688
|
T | C | 1 | a0010c0014t0001g0352 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.*45-3330A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164688 | ||||||
| chr22:42164752
|
A | C | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*45-3394T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164752 | ||||||
| chr22:42164966
|
T | C | 10 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.*45-3608A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42164966 | ||||||
| chr22:42165072
|
G | C | 1 | a0001c0001t0010g0002 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.*44+3537C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42165072 | ||||||
| chr22:42165277
|
G | A | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*44+3332C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42165277 | ||||||
| chr22:42165359
|
A | G | 83 | a0001c0002t0001g0270a0001c0002t0001g0278a0001c0002t0001g0280others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.*44+3250T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42165359 | ||||||
| chr22:42165520
|
G | C | 1 | a0001c0001t0001g0134 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.*44+3089C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42165520 | ||||||
| chr22:42165852
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*44+2757A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42165852 | ||||||
| chr22:42165919
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*44+2690C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42165919 | ||||||
| chr22:42165931
|
C | G | 7 | a0002c0003t0001g0052a0002c0003t0001g0053a0002c0003t0001g0054others(4): Show | 7 | HG00738.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.*44+2678G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42165931 | ||||||
| chr22:42166357
|
C | T | 1 | a0003c0004t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*44+2252G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166357 | ||||||
| chr22:42166469
|
G | A | 14 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(11): Show | 14 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.*44+2140C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166469 | ||||||
| chr22:42166563
|
C | T | 19 | a0001c0001t0002g0014a0001c0001t0002g0091a0001c0001t0002g0092others(16): Show | 19 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.*44+2046G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166563 | ||||||
| chr22:42166609
|
C | CA | 31 | a0001c0001t0001g0267a0001c0001t0002g0091a0001c0001t0002g0092others(28): Show | 31 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.*44+1999dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166609 | ||||||
| chr22:42166611
|
A | G | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*44+1998T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166611 | ||||||
| chr22:42166634
|
G | C | 10 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.*44+1975C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166634 | ||||||
| chr22:42166647
|
T | TAGGA | 4 | a0002c0003t0001g0020a0002c0003t0001g0038a0002c0003t0001g0039others(1): Show | 4 | HG02027.hp2 HG02080.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.*44+1958_*44+1961d others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166647 | ||||||
| chr22:42166701
|
G | C | 15 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0012t0002g0231others(12): Show | 15 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.*44+1908C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166701 | ||||||
| chr22:42166834
|
C | T | 1 | a0001c0002t0001g0301 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.*44+1775G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166834 | ||||||
| chr22:42166972
|
C | T | 1 | a0001c0002t0001g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*44+1637G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166972 | ||||||
| chr22:42166990
|
G | A | 10 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.*44+1619C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42166990 | ||||||
| chr22:42167160
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.*44+1449G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167160 | ||||||
| chr22:42167251
|
A | G | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*44+1358T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167251 | ||||||
| chr22:42167264
|
T | C | 3 | a0001c0001t0004g0095a0007c0011t0004g0244a0007c0011t0004g0254 | 3 | HG02486.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.*44+1345A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167264 | ||||||
| chr22:42167302
|
C | T | 77 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(74): Show | 77 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.*44+1307G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167302 | ||||||
| chr22:42167312
|
T | G | 2 | a0001c0001t0002g0096a0001c0002t0002g0138 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.*44+1297A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167312 | ||||||
| chr22:42167380
|
G | A | 2 | a0001c0002t0001g0279a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.*44+1229C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167380 | ||||||
| chr22:42167400
|
T | A | 1 | a0001c0002t0001g0324 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.*44+1209A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167400 | ||||||
| chr22:42167519
|
AT | A | 69 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.*44+1089delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167519 | ||||||
| chr22:42167523
|
T | G | 13 | a0001c0002t0001g0278a0001c0002t0001g0280a0001c0002t0001g0283others(10): Show | 13 | HG00597.hp2 HG00621.hp2 HG04184.hp2 others(10): Show |
intron_variant | MODIFIER | c.*44+1086A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167523 | ||||||
| chr22:42167526
|
T | G | 69 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.*44+1083A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167526 | ||||||
| chr22:42167588
|
C | G | 2 | a0002c0003t0001g0081a0002c0003t0001g0082 | 2 | NA19010.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.*44+1021G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167588 | ||||||
| chr22:42167883
|
C | T | 17 | a0001c0001t0001g0153a0002c0003t0001g0018a0002c0003t0001g0022others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.*44+726G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167883 | ||||||
| chr22:42167889
|
A | AT | 9 | a0001c0001t0001g0017a0001c0001t0004g0095a0001c0002t0001g0255others(6): Show | 9 | HG01099.hp2 HG02027.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.*44+719dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167889 | ||||||
| chr22:42167927
|
C | T | 69 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.*44+682G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42167927 | ||||||
| chr22:42168177
|
T | C | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*44+432A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42168177 | ||||||
| chr22:42168298
|
C | T | 69 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.*44+311G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42168298 | ||||||
| chr22:42168306
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.*44+303T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42168306 | ||||||
| chr22:42168524
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*44+85C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 5/5 | chr22 | 42168524 | ||||||
| chr22:42168761
|
G | A | 1 | a0001c0002t0001g0306 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5800-25C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42168761 | ||||||
| chr22:42168896
|
G | C | 2 | a0001c0002t0001g0346a0002c0003t0001g0298 | 2 | NA19081.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.5800-160C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42168896 | ||||||
| chr22:42168927
|
T | TA | 4 | a0004c0005t0002g0229a0004c0005t0002g0237a0004c0005t0002g0240others(1): Show | 4 | HG03041.hp1 HG03139.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.5800-192dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42168927 | ||||||
| chr22:42168997
|
C | T | 1 | a0001c0001t0015g0337 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5800-261G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42168997 | ||||||
| chr22:42169054
|
C | G | 1 | a0001c0001t0001g0181 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5800-318G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169054 | ||||||
| chr22:42169194
|
G | A | 25 | a0001c0001t0001g0116a0001c0001t0002g0096a0001c0001t0013g0114others(22): Show | 25 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.5800-458C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169194 | ||||||
| chr22:42169348
|
G | A | 1 | a0003c0004t0003g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5799+499C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169348 | ||||||
| chr22:42169355
|
G | C | 1 | a0001c0002t0014g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5799+492C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169355 | ||||||
| chr22:42169443
|
C | T | 2 | a0002c0003t0001g0074a0002c0003t0017g0066 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5799+404G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169443 | ||||||
| chr22:42169452
|
G | A | 1 | a0002c0003t0017g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5799+395C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169452 | ||||||
| chr22:42169621
|
T | C | 11 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5799+226A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169621 | ||||||
| chr22:42169675
|
C | T | 13 | a0004c0005t0002g0229a0004c0005t0002g0230a0004c0005t0002g0232others(10): Show | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.5799+172G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169675 | ||||||
| chr22:42169771
|
C | A | 2 | a0001c0001t0002g0096a0001c0002t0001g0301 | 2 | HG03516.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.5799+76G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169771 | ||||||
| chr22:42169829
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5799+18A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 4/5 | chr22 | 42169829 | ||||||
| chr22:42169918
|
T | C | 1 | a0007c0011t0004g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5750-22A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42169918 | ||||||
| chr22:42169944
|
T | C | 35 | a0001c0001t0001g0267a0001c0001t0002g0014a0001c0001t0002g0091others(32): Show | 35 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.5750-48A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42169944 | ||||||
| chr22:42169977
|
T | A | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5750-81A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42169977 | ||||||
| chr22:42170095
|
G | T | 54 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(51): Show | 54 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.5750-199C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170095 | ||||||
| chr22:42170308
|
G | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.5750-412C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170308 | ||||||
| chr22:42170335
|
T | TA | 18 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(15): Show | 18 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.5750-440dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170335 | ||||||
| chr22:42170335
|
TA | T | 45 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0002g0091others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.5750-440delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170335 | ||||||
| chr22:42170335
|
TAA | T | 71 | a0001c0001t0001g0017a0002c0003t0001g0010a0002c0003t0001g0018others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.5750-441_5750-440d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170335 | ||||||
| chr22:42170355
|
C | T | 1 | a0001c0001t0013g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5750-459G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170355 | ||||||
| chr22:42170362
|
G | T | 1 | a0002c0003t0001g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5750-466C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170362 | ||||||
| chr22:42170411
|
G | A | 21 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0106others(18): Show | 21 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.5750-515C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170411 | ||||||
| chr22:42170626
|
C | CA | 30 | a0001c0001t0001g0099a0001c0001t0001g0201a0001c0002t0001g0265others(27): Show | 30 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.5750-731dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAA | 15 | a0001c0001t0001g0116a0001c0002t0001g0269a0001c0002t0001g0308others(12): Show | 15 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5750-732_5750-731d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAA | 28 | a0001c0002t0001g0090a0002c0003t0001g0010a0002c0003t0001g0020others(25): Show | 28 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.5750-733_5750-731d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAA | 15 | a0002c0003t0001g0042a0002c0003t0001g0045a0002c0003t0001g0046others(12): Show | 15 | HG02071.hp1 HG02083.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.5750-734_5750-731d others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA | 13 | a0001c0001t0001g0017a0002c0003t0001g0023a0002c0003t0001g0025others(10): Show | 13 | HG00140.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.5750-737_5750-731d others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0267a0002c0003t0001g0024a0002c0003t0001g0026others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5750-738_5750-731d others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA others(2): Show |
9 | a0001c0012t0002g0231a0002c0003t0001g0022a0002c0007t0001g0078others(6): Show | 9 | HG00323.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.5750-739_5750-731d others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA others(3): Show |
3 | a0004c0005t0002g0232a0004c0005t0002g0234a0004c0005t0002g0242 | 3 | HG02723.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5750-740_5750-731d others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA others(4): Show |
4 | a0004c0005t0002g0230a0004c0005t0002g0237a0004c0005t0002g0240others(1): Show | 4 | HG02622.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.5750-741_5750-731d others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA others(6): Show |
3 | a0005c0009t0008g0353a0005c0009t0008g0355a0016c0029t0022g0354 | 3 | HG02572.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5750-743_5750-731d others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | HG02109.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.5750-749_5750-731d others(21): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
C | CAAAAAAA others(13): Show |
1 | a0001c0010t0006g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5750-750_5750-731d others(22): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
CA | C | 7 | a0001c0001t0002g0344a0001c0001t0013g0114a0001c0002t0001g0316others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.5750-731delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
CAAAA | C | 8 | a0001c0001t0002g0014a0001c0001t0002g0248a0001c0001t0002g0350others(5): Show | 8 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.5750-734_5750-731d others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0001g0007a0001c0001t0001g0164a0001c0001t0001g0179others(6): Show | 9 | HG00099.hp1 HG00741.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.5750-738_5750-731d others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
CAAAAAAA others(2): Show |
C | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.5750-739_5750-731d others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5750-741_5750-731d others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170626
|
CAAAAAAA others(6): Show |
C | 11 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(8): Show | 11 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.5750-743_5750-731d others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170626 | ||||||
| chr22:42170643
|
A | G | 11 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(8): Show | 11 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.5750-747T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170643 | ||||||
| chr22:42170747
|
G | A | 11 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5750-851C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170747 | ||||||
| chr22:42170850
|
C | T | 1 | a0008c0024t0001g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5750-954G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42170850 | ||||||
| chr22:42171084
|
T | C | 25 | a0001c0001t0001g0116a0001c0001t0013g0114a0001c0002t0001g0327others(22): Show | 25 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.5750-1188A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171084 | ||||||
| chr22:42171351
|
A | AGCC | 3 | a0001c0001t0001g0293a0001c0001t0015g0337a0001c0002t0001g0279 | 3 | HG03453.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5750-1458_5750-145 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171351 | ||||||
| chr22:42171424
|
C | T | 2 | a0001c0002t0001g0255a0001c0002t0001g0301 | 2 | HG02027.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.5750-1528G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171424 | ||||||
| chr22:42171433
|
A | G | 9 | a0001c0001t0002g0014a0001c0001t0002g0248a0001c0001t0002g0350others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5750-1537T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171433 | ||||||
| chr22:42171445
|
A | G | 70 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(67): Show | 70 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.5750-1549T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171445 | ||||||
| chr22:42171545
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.5750-1649C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171545 | ||||||
| chr22:42171547
|
G | A | 1 | a0003c0004t0003g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-1651C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171547 | ||||||
| chr22:42171670
|
C | T | 8 | a0001c0001t0002g0014a0001c0001t0002g0248a0001c0001t0002g0350others(5): Show | 8 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.5750-1774G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171670 | ||||||
| chr22:42171671
|
G | A | 1 | a0003c0004t0001g0117 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5750-1775C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171671 | ||||||
| chr22:42171697
|
T | C | 1 | a0001c0002t0001g0097 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.5750-1801A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171697 | ||||||
| chr22:42171819
|
C | T | 8 | a0001c0001t0002g0014a0001c0001t0002g0248a0001c0001t0002g0350others(5): Show | 8 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.5750-1923G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171819 | ||||||
| chr22:42171880
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5750-1984T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42171880 | ||||||
| chr22:42172029
|
C | T | 14 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(11): Show | 14 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.5750-2133G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42172029 | ||||||
| chr22:42172317
|
G | A | 4 | a0002c0003t0001g0044a0002c0003t0001g0047a0002c0003t0001g0048others(1): Show | 4 | HG02071.hp1 NA18951.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.5750-2421C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42172317 | ||||||
| chr22:42172411
|
A | G | 1 | a0003c0026t0001g0345 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5750-2515T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42172411 | ||||||
| chr22:42172630
|
T | TCCTCATT others(4): Show |
1 | a0001c0001t0001g0130 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.5750-2745_5750-273 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42172630 | ||||||
| chr22:42172739
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.5750-2843A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42172739 | ||||||
| chr22:42172903
|
A | G | 1 | a0002c0003t0001g0067 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.5750-3007T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42172903 | ||||||
| chr22:42173018
|
T | C | 128 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0099others(125): Show | 128 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.5750-3122A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173018 | ||||||
| chr22:42173118
|
G | C | 3 | a0001c0001t0001g0149a0001c0001t0001g0190a0001c0017t0001g0150 | 3 | HG01943.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.5750-3222C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173118 | ||||||
| chr22:42173126
|
GA | G | 127 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0099others(124): Show | 127 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.5750-3231delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173126 | ||||||
| chr22:42173164
|
C | G | 11 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0210others(8): Show | 11 | HG00639.hp2 HG01361.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.5750-3268G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173164 | ||||||
| chr22:42173203
|
C | A | 1 | a0003c0004t0001g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5750-3307G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173203 | ||||||
| chr22:42173204
|
G | C | 1 | a0003c0004t0001g0117 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5750-3308C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173204 | ||||||
| chr22:42173241
|
A | AT | 21 | a0001c0001t0003g0012a0002c0003t0001g0022a0002c0003t0001g0023others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.5750-3346dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173241 | ||||||
| chr22:42173243
|
T | TAA | 10 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.5750-3349_5750-334 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173243 | ||||||
| chr22:42173243
|
T | TTA | 86 | a0001c0001t0001g0017a0001c0001t0001g0267a0001c0001t0002g0014others(83): Show | 86 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.5750-3348_5750-334 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173243 | ||||||
| chr22:42173244
|
A | T | 2 | a0001c0002t0001g0288a0002c0003t0001g0018 | 2 | HG01993.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.5750-3348T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173244 | ||||||
| chr22:42173290
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5750-3394G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173290 | ||||||
| chr22:42173292
|
C | A | 70 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(67): Show | 70 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.5750-3396G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173292 | ||||||
| chr22:42173316
|
A | G | 1 | a0001c0002t0001g0299 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5750-3420T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173316 | ||||||
| chr22:42173348
|
A | G | 1 | a0003c0026t0001g0345 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5750-3452T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173348 | ||||||
| chr22:42173349
|
T | C | 3 | a0001c0002t0001g0303a0001c0002t0001g0323a0001c0002t0001g0325 | 3 | NA19004.hp1 NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.5750-3453A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173349 | ||||||
| chr22:42173391
|
T | G | 1 | a0001c0002t0002g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5750-3495A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173391 | ||||||
| chr22:42173493
|
TG | T | 11 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0013others(8): Show | 11 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.5750-3598delC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173493 | ||||||
| chr22:42173672
|
T | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.5750-3776A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173672 | ||||||
| chr22:42173753
|
A | G | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-3857T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173753 | ||||||
| chr22:42173864
|
C | T | 128 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0099others(125): Show | 128 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.5750-3968G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173864 | ||||||
| chr22:42173993
|
C | T | 125 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0099others(122): Show | 125 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.5750-4097G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42173993 | ||||||
| chr22:42174221
|
T | TA | 11 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5750-4326dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174221 | ||||||
| chr22:42174434
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5750-4538G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174434 | ||||||
| chr22:42174452
|
G | A | 108 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 108 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.5750-4556C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174452 | ||||||
| chr22:42174648
|
T | C | 1 | a0001c0002t0001g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5750-4752A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174648 | ||||||
| chr22:42174720
|
A | AT | 6 | a0001c0001t0001g0154a0001c0001t0001g0263a0001c0001t0001g0264others(3): Show | 6 | HG01109.hp1 HG01928.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.5750-4825dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174720 | ||||||
| chr22:42174720
|
A | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5750-4824T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174720 | ||||||
| chr22:42174721
|
T | A | 70 | a0001c0001t0001g0201a0001c0002t0001g0257a0001c0002t0001g0277others(67): Show | 70 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.5750-4825A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174721 | ||||||
| chr22:42174733
|
T | C | 7 | a0001c0001t0002g0248a0001c0001t0002g0350a0001c0006t0002g0246others(4): Show | 7 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.5750-4837A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174733 | ||||||
| chr22:42174763
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5749+4846G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174763 | ||||||
| chr22:42174768
|
G | C | 1 | a0001c0002t0001g0291 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.5749+4841C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174768 | ||||||
| chr22:42174797
|
G | T | 1 | a0001c0001t0002g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5749+4812C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174797 | ||||||
| chr22:42174811
|
A | G | 1 | a0001c0002t0014g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5749+4798T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174811 | ||||||
| chr22:42174831
|
C | G | 1 | a0001c0002t0001g0306 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5749+4778G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174831 | ||||||
| chr22:42174831
|
C | T | 2 | a0002c0007t0001g0078a0002c0007t0001g0085 | 2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.5749+4778G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174831 | ||||||
| chr22:42174842
|
C | T | 237 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 237 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.5749+4767G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174842 | ||||||
| chr22:42174849
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.5749+4760G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174849 | ||||||
| chr22:42174851
|
C | T | 25 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0142others(22): Show | 25 | HG00544.hp2 HG02523.hp1 NA18947.hp1 others(22): Show |
intron_variant | MODIFIER | c.5749+4758G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174851 | ||||||
| chr22:42174852
|
G | A | 26 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0142others(23): Show | 26 | HG00544.hp2 HG02523.hp1 HG03927.hp2 others(23): Show |
intron_variant | MODIFIER | c.5749+4757C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174852 | ||||||
| chr22:42174859
|
C | A | 1 | a0001c0002t0001g0325 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.5749+4750G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174859 | ||||||
| chr22:42174907
|
C | T | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5749+4702G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174907 | ||||||
| chr22:42174926
|
T | C | 8 | a0001c0001t0002g0014a0001c0001t0003g0012a0001c0001t0003g0013others(5): Show | 8 | HG02486.hp1 HG02809.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.5749+4683A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174926 | ||||||
| chr22:42174931
|
C | A | 1 | a0001c0002t0001g0310 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5749+4678G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174931 | ||||||
| chr22:42174932
|
G | A | 1 | a0003c0004t0001g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.5749+4677C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174932 | ||||||
| chr22:42174951
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5749+4658G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42174951 | ||||||
| chr22:42175021
|
C | T | 1 | a0001c0001t0015g0337 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5749+4588G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175021 | ||||||
| chr22:42175022
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.5749+4587C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175022 | ||||||
| chr22:42175096
|
C | T | 7 | a0001c0002t0001g0329a0001c0002t0001g0331a0001c0002t0001g0332others(4): Show | 7 | NA18969.hp1 NA18975.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+4513G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175096 | ||||||
| chr22:42175159
|
A | G | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+4450T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175159 | ||||||
| chr22:42175197
|
A | G | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5749+4412T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175197 | ||||||
| chr22:42175390
|
G | C | 1 | a0001c0002t0001g0277 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.5749+4219C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175390 | ||||||
| chr22:42175402
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.5749+4207C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175402 | ||||||
| chr22:42175433
|
C | T | 1 | a0001c0001t0016g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5749+4176G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175433 | ||||||
| chr22:42175590
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5749+4019G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175590 | ||||||
| chr22:42175631
|
G | C | 4 | a0001c0002t0001g0256a0001c0002t0001g0260a0001c0002t0001g0309others(1): Show | 4 | HG00099.hp2 HG01943.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.5749+3978C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175631 | ||||||
| chr22:42175723
|
A | G | 11 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(8): Show | 11 | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.5749+3886T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175723 | ||||||
| chr22:42175900
|
C | T | 1 | a0001c0002t0001g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5749+3709G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175900 | ||||||
| chr22:42175901
|
C | T | 54 | a0001c0002t0001g0278a0001c0002t0001g0280a0001c0002t0001g0283others(51): Show | 54 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.5749+3708G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42175901 | ||||||
| chr22:42176003
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0170 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.5749+3606G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176003 | ||||||
| chr22:42176120
|
C | T | 8 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(5): Show | 8 | NA18949.hp1 NA18962.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.5749+3489G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176120 | ||||||
| chr22:42176129
|
A | C | 7 | a0001c0001t0002g0248a0001c0001t0002g0350a0001c0006t0002g0246others(4): Show | 7 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+3480T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176129 | ||||||
| chr22:42176241
|
T | C | 13 | a0004c0005t0002g0229a0004c0005t0002g0230a0004c0005t0002g0232others(10): Show | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.5749+3368A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176241 | ||||||
| chr22:42176351
|
C | A | 25 | a0001c0001t0001g0116a0001c0001t0002g0096a0001c0001t0013g0114others(22): Show | 25 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.5749+3258G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176351 | ||||||
| chr22:42176357
|
G | A | 69 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.5749+3252C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176357 | ||||||
| chr22:42176378
|
A | AG | 22 | a0001c0002t0018g0261a0003c0004t0001g0104a0003c0004t0001g0105others(19): Show | 22 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.5749+3230dupC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176378 | ||||||
| chr22:42176378
|
AG | A | 217 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.5749+3230delC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176378 | ||||||
| chr22:42176382
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.5749+3227C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176382 | ||||||
| chr22:42176450
|
G | A | 1 | a0004c0005t0002g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5749+3159C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176450 | ||||||
| chr22:42176541
|
C | T | 69 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.5749+3068G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176541 | ||||||
| chr22:42176546
|
G | A | 1 | a0001c0002t0001g0310 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5749+3063C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176546 | ||||||
| chr22:42176724
|
C | A | 2 | a0003c0004t0001g0107a0003c0004t0001g0108 | 2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.5749+2885G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176724 | ||||||
| chr22:42176824
|
G | A | 1 | a0002c0003t0001g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5749+2785C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42176824 | ||||||
| chr22:42177133
|
C | G | 114 | a0001c0001t0001g0017a0001c0001t0001g0267a0001c0001t0002g0091others(111): Show | 114 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.5749+2476G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42177133 | ||||||
| chr22:42177152
|
C | T | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5749+2457G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42177152 | ||||||
| chr22:42177523
|
A | T | 1 | a0001c0002t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5749+2086T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42177523 | ||||||
| chr22:42177675
|
C | T | 1 | a0004c0005t0002g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5749+1934G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42177675 | ||||||
| chr22:42177804
|
G | A | 11 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5749+1805C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42177804 | ||||||
| chr22:42177950
|
G | T | 66 | a0001c0002t0001g0278a0001c0002t0001g0280a0001c0002t0001g0283others(63): Show | 66 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.5749+1659C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42177950 | ||||||
| chr22:42177952
|
A | T | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5749+1657T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42177952 | ||||||
| chr22:42178252
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | NA18973.hp2 NA18995.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.5749+1357C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178252 | ||||||
| chr22:42178322
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5749+1287A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178322 | ||||||
| chr22:42178448
|
AG | A | 23 | a0001c0001t0001g0116a0001c0001t0013g0114a0002c0003t0001g0079others(20): Show | 23 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.5749+1160delC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178448 | ||||||
| chr22:42178549
|
C | T | 86 | a0001c0001t0001g0017a0001c0002t0001g0278a0001c0002t0001g0280others(83): Show | 86 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.5749+1060G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178549 | ||||||
| chr22:42178585
|
C | CT | 13 | a0001c0002t0001g0266a0001c0002t0001g0320a0001c0002t0002g0300others(10): Show | 13 | HG00438.hp1 HG00438.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.5749+1023dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178585 | ||||||
| chr22:42178585
|
CT | C | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.5749+1023delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178585 | ||||||
| chr22:42178585
|
CTT | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0130a0001c0001t0001g0164others(4): Show | 7 | HG01069.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+1022_5749+102 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178585 | ||||||
| chr22:42178694
|
T | G | 1 | a0007c0011t0004g0254 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5749+915A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178694 | ||||||
| chr22:42178723
|
T | C | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5749+886A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178723 | ||||||
| chr22:42178824
|
C | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.5749+785G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178824 | ||||||
| chr22:42178830
|
G | A | 2 | a0001c0002t0001g0339a0011c0020t0001g0340 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5749+779C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42178830 | ||||||
| chr22:42179037
|
T | TA | 71 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0002g0094others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.5749+571dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179037 | ||||||
| chr22:42179037
|
TA | T | 13 | a0001c0001t0001g0101a0001c0001t0001g0130a0001c0001t0001g0154others(10): Show | 13 | HG00323.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.5749+571delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179037 | ||||||
| chr22:42179037
|
TAA | T | 6 | a0001c0001t0002g0014a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+570_5749+571d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179037 | ||||||
| chr22:42179039
|
A | T | 1 | a0001c0001t0003g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5749+570T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179039 | ||||||
| chr22:42179040
|
A | T | 6 | a0001c0001t0002g0014a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+569T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179040 | ||||||
| chr22:42179084
|
G | A | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+525C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179084 | ||||||
| chr22:42179375
|
G | GA | 7 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(4): Show | 7 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+233dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179375 | ||||||
| chr22:42179405
|
A | G | 1 | a0001c0001t0013g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5749+204T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179405 | ||||||
| chr22:42179490
|
CA | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.5749+118delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179490 | ||||||
| chr22:42179490
|
CAA | C | 42 | a0001c0001t0001g0017a0001c0001t0001g0130a0001c0001t0001g0202others(39): Show | 42 | HG00544.hp1 HG00738.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.5749+117_5749+118d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179490 | ||||||
| chr22:42179490
|
CAAA | C | 11 | a0004c0005t0002g0230a0004c0005t0002g0232a0004c0005t0002g0233others(8): Show | 11 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.5749+116_5749+118d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179490 | ||||||
| chr22:42179490
|
CAAAAAAA others(2): Show |
C | 6 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0109others(3): Show | 6 | HG00639.hp1 HG01243.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.5749+110_5749+118d others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179490 | ||||||
| chr22:42179507
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0201 | 2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.5749+102T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179507 | ||||||
| chr22:42179551
|
A | T | 7 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(4): Show | 7 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5749+58T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 3/5 | chr22 | 42179551 | ||||||
| chr22:42179713
|
G | A | 1 | a0003c0004t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5656-11C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42179713 | ||||||
| chr22:42179759
|
A | G | 2 | a0001c0002t0001g0284a0001c0002t0001g0285 | 2 | NA18939.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.5656-57T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42179759 | ||||||
| chr22:42179942
|
G | A | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.5656-240C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42179942 | ||||||
| chr22:42180146
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.5656-444G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42180146 | ||||||
| chr22:42180714
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5656-1012G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42180714 | ||||||
| chr22:42180754
|
C | G | 1 | a0001c0002t0001g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5656-1052G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42180754 | ||||||
| chr22:42180854
|
C | G | 7 | a0001c0001t0002g0248a0001c0001t0002g0350a0001c0006t0002g0246others(4): Show | 7 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.5656-1152G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42180854 | ||||||
| chr22:42180962
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5656-1260G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42180962 | ||||||
| chr22:42180985
|
T | C | 1 | a0003c0004t0003g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.5656-1283A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42180985 | ||||||
| chr22:42180994
|
G | A | 1 | a0001c0002t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5656-1292C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42180994 | ||||||
| chr22:42181398
|
G | T | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5656-1696C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42181398 | ||||||
| chr22:42181432
|
CTGCTGCC others(3): Show |
C | 12 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(9): Show | 12 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.5656-1740_5656-173 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42181432 | ||||||
| chr22:42181598
|
C | CT | 17 | a0001c0001t0001g0195a0001c0001t0001g0213a0001c0001t0002g0344others(14): Show | 17 | HG01361.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.5656-1897dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42181598 | ||||||
| chr22:42181598
|
CT | C | 14 | a0001c0001t0001g0216a0001c0001t0001g0222a0001c0001t0001g0224others(11): Show | 14 | HG00673.hp2 HG01256.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.5656-1897delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42181598 | ||||||
| chr22:42181859
|
A | C | 1 | a0001c0002t0002g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5656-2157T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42181859 | ||||||
| chr22:42182048
|
G | T | 53 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(50): Show | 53 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.5656-2346C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42182048 | ||||||
| chr22:42182590
|
T | C | 101 | a0001c0001t0001g0267a0001c0001t0002g0091a0001c0001t0002g0092others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.5656-2888A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42182590 | ||||||
| chr22:42182603
|
G | A | 30 | a0001c0002t0001g0262a0001c0002t0001g0272a0001c0002t0001g0284others(27): Show | 30 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.5656-2901C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42182603 | ||||||
| chr22:42182771
|
C | G | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5656-3069G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42182771 | ||||||
| chr22:42182925
|
C | T | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5656-3223G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42182925 | ||||||
| chr22:42183045
|
C | T | 45 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(42): Show | 45 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.5656-3343G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183045 | ||||||
| chr22:42183089
|
G | C | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5656-3387C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183089 | ||||||
| chr22:42183303
|
TTA | T | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.5656-3603_5656-360 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183303 | ||||||
| chr22:42183308
|
T | C | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5656-3606A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183308 | ||||||
| chr22:42183371
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5656-3669C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183371 | ||||||
| chr22:42183415
|
C | A | 1 | a0001c0002t0001g0270 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5656-3713G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183415 | ||||||
| chr22:42183514
|
T | C | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.5656-3812A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183514 | ||||||
| chr22:42183646
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5656-3944A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183646 | ||||||
| chr22:42183652
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5656-3950G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183652 | ||||||
| chr22:42183655
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5656-3953T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183655 | ||||||
| chr22:42183776
|
C | CT | 32 | a0001c0001t0001g0192a0001c0001t0001g0267a0001c0001t0002g0091others(29): Show | 32 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.5656-4075dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183776 | ||||||
| chr22:42183776
|
CT | C | 12 | a0002c0003t0001g0052a0002c0003t0001g0053a0002c0003t0001g0054others(9): Show | 12 | HG00738.hp1 HG01074.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.5656-4075delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183776 | ||||||
| chr22:42183802
|
C | T | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5656-4100G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183802 | ||||||
| chr22:42183917
|
T | C | 113 | a0001c0001t0001g0017a0001c0001t0001g0201a0001c0001t0001g0245others(110): Show | 113 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.5656-4215A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183917 | ||||||
| chr22:42183956
|
A | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5656-4254T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42183956 | ||||||
| chr22:42184152
|
G | A | 2 | a0001c0002t0001g0313a0001c0002t0002g0259 | 2 | HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.5656-4450C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184152 | ||||||
| chr22:42184560
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5656-4858A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184560 | ||||||
| chr22:42184631
|
G | T | 1 | a0001c0002t0001g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5656-4929C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184631 | ||||||
| chr22:42184632
|
A | C | 1 | a0001c0002t0001g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5656-4930T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184632 | ||||||
| chr22:42184676
|
T | C | 1 | a0001c0002t0001g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5656-4974A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184676 | ||||||
| chr22:42184917
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG00280.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.5656-5215G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184917 | ||||||
| chr22:42184927
|
A | C | 122 | a0001c0001t0001g0017a0001c0001t0001g0267a0001c0001t0002g0014others(119): Show | 122 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.5656-5225T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184927 | ||||||
| chr22:42184969
|
A | G | 354 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.5656-5267T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184969 | ||||||
| chr22:42184976
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.5656-5274A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42184976 | ||||||
| chr22:42185035
|
C | G | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5656-5333G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42185035 | ||||||
| chr22:42185072
|
G | T | 1 | a0001c0002t0001g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5656-5370C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42185072 | ||||||
| chr22:42185242
|
C | T | 17 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.5656-5540G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42185242 | ||||||
| chr22:42185398
|
A | C | 2 | a0001c0001t0001g0267a0001c0012t0002g0231 | 2 | HG02258.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5656-5696T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42185398 | ||||||
| chr22:42185503
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.5656-5801C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42185503 | ||||||
| chr22:42185529
|
T | C | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5656-5827A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42185529 | ||||||
| chr22:42186281
|
A | T | 1 | a0006c0008t0001g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5656-6579T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42186281 | ||||||
| chr22:42186363
|
A | G | 1 | a0002c0003t0021g0087 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5656-6661T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42186363 | ||||||
| chr22:42186383
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5656-6681G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42186383 | ||||||
| chr22:42186388
|
T | C | 121 | a0001c0001t0001g0201a0001c0001t0001g0267a0001c0001t0002g0014others(118): Show | 121 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.5656-6686A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42186388 | ||||||
| chr22:42186505
|
TATTAA | T | 11 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5656-6808_5656-680 others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42186505 | ||||||
| chr22:42186668
|
C | A | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5656-6966G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42186668 | ||||||
| chr22:42186763
|
C | G | 1 | a0007c0011t0004g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5656-7061G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42186763 | ||||||
| chr22:42187322
|
T | C | 1 | a0002c0003t0001g0020 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5656-7620A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42187322 | ||||||
| chr22:42187639
|
G | A | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5656-7937C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42187639 | ||||||
| chr22:42187686
|
G | A | 2 | a0001c0016t0001g0311a0013c0015t0001g0312 | 2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.5656-7984C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42187686 | ||||||
| chr22:42187737
|
T | C | 2 | a0001c0010t0006g0008a0001c0010t0006g0009 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.5656-8035A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42187737 | ||||||
| chr22:42187904
|
G | A | 79 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(76): Show | 79 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.5656-8202C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42187904 | ||||||
| chr22:42188008
|
C | A | 1 | a0001c0001t0001g0228 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.5656-8306G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188008 | ||||||
| chr22:42188065
|
A | G | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.5656-8363T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188065 | ||||||
| chr22:42188293
|
C | CA | 76 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(73): Show | 76 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.5656-8592dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAA | 20 | a0001c0001t0001g0251a0001c0001t0002g0093a0001c0002t0001g0256others(17): Show | 20 | HG00099.hp2 HG00438.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.5656-8593_5656-859 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAA | 8 | a0001c0001t0001g0245a0001c0001t0002g0248a0001c0001t0002g0350others(5): Show | 8 | HG01433.hp2 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.5656-8594_5656-859 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAA | 18 | a0001c0001t0013g0114a0001c0002t0001g0327a0001c0006t0002g0249others(15): Show | 18 | HG00639.hp1 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.5656-8596_5656-859 others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAA | 19 | a0001c0001t0001g0177a0001c0001t0001g0201a0002c0003t0001g0018others(16): Show | 19 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.5656-8597_5656-859 others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA | 8 | a0001c0001t0001g0203a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG01175.hp2 HG01496.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.5656-8598_5656-859 others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0137a0001c0001t0001g0156a0001c0001t0001g0202others(5): Show | 8 | HG00639.hp2 HG00735.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.5656-8599_5656-859 others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA others(2): Show |
38 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0116others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.5656-8600_5656-859 others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA others(3): Show |
32 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0139others(29): Show | 32 | HG00621.hp1 HG00642.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.5656-8601_5656-859 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA others(4): Show |
17 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0148others(14): Show | 17 | HG00673.hp2 HG01069.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.5656-8602_5656-859 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA others(5): Show |
9 | a0001c0001t0001g0136a0001c0001t0001g0151a0001c0001t0001g0175others(6): Show | 9 | HG00544.hp2 NA18956.hp2 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.5656-8603_5656-859 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA others(6): Show |
2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5656-8604_5656-859 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5656-8606_5656-859 others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
CAAAAAAA others(1): Show |
C | 19 | a0001c0001t0001g0267a0001c0012t0002g0231a0002c0003t0001g0047others(16): Show | 19 | HG00673.hp1 HG02258.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.5656-8599_5656-859 others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
CAAAAAAA others(2): Show |
C | 59 | a0001c0002t0001g0278a0001c0002t0001g0280a0001c0002t0001g0283others(56): Show | 59 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.5656-8600_5656-859 others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
CAAAAAAA others(3): Show |
C | 3 | a0002c0003t0001g0063a0002c0003t0001g0074a0002c0003t0001g0082 | 3 | HG02895.hp1 NA19054.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.5656-8601_5656-859 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188293
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0003t0001g0031 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5656-8602_5656-859 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188293 | ||||||
| chr22:42188356
|
G | A | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.5656-8654C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188356 | ||||||
| chr22:42188383
|
C | T | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.5656-8681G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188383 | ||||||
| chr22:42188389
|
G | A | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.5656-8687C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188389 | ||||||
| chr22:42188408
|
C | A | 1 | a0001c0002t0001g0322 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.5656-8706G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188408 | ||||||
| chr22:42188460
|
G | C | 233 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(230): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.5656-8758C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188460 | ||||||
| chr22:42188520
|
A | T | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5656-8818T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188520 | ||||||
| chr22:42188566
|
T | G | 1 | a0006c0008t0001g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5656-8864A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188566 | ||||||
| chr22:42188606
|
A | C | 1 | a0001c0001t0001g0199 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.5656-8904T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188606 | ||||||
| chr22:42188615
|
T | G | 7 | a0001c0002t0001g0329a0001c0002t0001g0331a0001c0002t0001g0332others(4): Show | 7 | NA18969.hp1 NA18975.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.5656-8913A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188615 | ||||||
| chr22:42188632
|
G | C | 1 | a0001c0002t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5656-8930C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188632 | ||||||
| chr22:42188912
|
G | A | 1 | a0001c0002t0001g0342 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5656-9210C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42188912 | ||||||
| chr22:42189233
|
T | C | 2 | a0001c0001t0001g0017a0005c0009t0001g0089 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5656-9531A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42189233 | ||||||
| chr22:42189298
|
T | A | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.5656-9596A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42189298 | ||||||
| chr22:42189325
|
T | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5656-9623A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42189325 | ||||||
| chr22:42189426
|
T | G | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5656-9724A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42189426 | ||||||
| chr22:42189433
|
G | A | 1 | a0001c0002t0001g0341 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.5656-9731C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42189433 | ||||||
| chr22:42189659
|
C | G | 3 | a0005c0009t0008g0353a0005c0009t0008g0355a0016c0029t0022g0354 | 3 | HG02572.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5656-9957G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42189659 | ||||||
| chr22:42189753
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5656-10051T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42189753 | ||||||
| chr22:42190067
|
T | C | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.5656-10365A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190067 | ||||||
| chr22:42190076
|
C | T | 26 | a0001c0001t0001g0267a0001c0001t0002g0091a0001c0001t0002g0092others(23): Show | 26 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.5656-10374G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190076 | ||||||
| chr22:42190459
|
G | GAC | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.5656-10759_5656-10 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190459 | ||||||
| chr22:42190584
|
G | A | 1 | a0001c0001t0003g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5656-10882C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190584 | ||||||
| chr22:42190643
|
A | T | 3 | a0001c0001t0004g0095a0007c0011t0004g0244a0007c0011t0004g0254 | 3 | HG02486.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5656-10941T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190643 | ||||||
| chr22:42190764
|
G | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5656-11062C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190764 | ||||||
| chr22:42190791
|
T | TTGA | 355 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(352): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.5656-11092_5656-11 others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190791 | ||||||
| chr22:42190874
|
T | C | 6 | a0002c0003t0001g0010a0002c0003t0001g0058a0002c0003t0001g0060others(3): Show | 6 | NA18747.hp1 NA18949.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.5656-11172A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190874 | ||||||
| chr22:42190924
|
G | A | 1 | a0001c0028t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5656-11222C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42190924 | ||||||
| chr22:42191020
|
CAAAACAA others(4): Show |
C | 7 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(4): Show | 7 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5656-11329_5656-11 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191020 | ||||||
| chr22:42191098
|
T | C | 2 | a0001c0002t0001g0349a0001c0002t0018g0261 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.5656-11396A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191098 | ||||||
| chr22:42191339
|
G | C | 5 | a0001c0002t0001g0294a0001c0002t0001g0295a0001c0002t0001g0296others(2): Show | 5 | HG02602.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.5656-11637C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191339 | ||||||
| chr22:42191350
|
C | T | 1 | a0003c0004t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5656-11648G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191350 | ||||||
| chr22:42191500
|
G | A | 1 | a0002c0003t0001g0050 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.5656-11798C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191500 | ||||||
| chr22:42191615
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5656-11913A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191615 | ||||||
| chr22:42191669
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5656-11967T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191669 | ||||||
| chr22:42191746
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5656-12044A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191746 | ||||||
| chr22:42191848
|
A | C | 7 | a0001c0002t0001g0329a0001c0002t0001g0331a0001c0002t0001g0332others(4): Show | 7 | NA18969.hp1 NA18975.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.5656-12146T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42191848 | ||||||
| chr22:42192436
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5656-12734G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42192436 | ||||||
| chr22:42192441
|
T | C | 1 | a0002c0003t0001g0081 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.5656-12739A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42192441 | ||||||
| chr22:42192464
|
G | C | 4 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.5656-12762C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42192464 | ||||||
| chr22:42192663
|
T | TCCTAAG | 13 | a0004c0005t0002g0229a0004c0005t0002g0230a0004c0005t0002g0232others(10): Show | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.5656-12967_5656-12 others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42192663 | ||||||
| chr22:42192756
|
G | A | 35 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(32): Show | 35 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.5656-13054C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42192756 | ||||||
| chr22:42192893
|
T | C | 2 | a0002c0003t0001g0064a0002c0003t0001g0065 | 2 | HG00438.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.5656-13191A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42192893 | ||||||
| chr22:42193046
|
G | A | 1 | a0001c0002t0001g0328 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5656-13344C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193046 | ||||||
| chr22:42193155
|
GAAAAGGA | G | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5656-13460_5656-13 others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193155 | ||||||
| chr22:42193249
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5656-13547C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193249 | ||||||
| chr22:42193250
|
C | A | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.5656-13548G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193250 | ||||||
| chr22:42193286
|
C | A | 11 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5656-13584G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193286 | ||||||
| chr22:42193458
|
A | C | 1 | a0001c0002t0001g0342 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5656-13756T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193458 | ||||||
| chr22:42193595
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5656-13893A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193595 | ||||||
| chr22:42193640
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5656-13938A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193640 | ||||||
| chr22:42193740
|
G | A | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5656-14038C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193740 | ||||||
| chr22:42193765
|
C | T | 1 | a0003c0026t0001g0345 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5656-14063G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193765 | ||||||
| chr22:42193849
|
A | G | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5656-14147T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42193849 | ||||||
| chr22:42194195
|
G | A | 2 | a0001c0002t0007g0102a0001c0002t0007g0103 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.5656-14493C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194195 | ||||||
| chr22:42194210
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5656-14508C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194210 | ||||||
| chr22:42194447
|
C | T | 1 | a0006c0008t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5656-14745G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194447 | ||||||
| chr22:42194451
|
C | T | 1 | a0002c0003t0001g0025 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.5656-14749G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194451 | ||||||
| chr22:42194598
|
G | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5656-14896C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194598 | ||||||
| chr22:42194608
|
C | CG | 5 | a0001c0001t0001g0165a0002c0003t0001g0068a0003c0004t0003g0125others(2): Show | 5 | HG02572.hp2 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5656-14907dupC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194608 | ||||||
| chr22:42194609
|
G | A | 6 | a0001c0001t0002g0014a0001c0001t0003g0012a0001c0001t0003g0013others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.5656-14907C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194609 | ||||||
| chr22:42194619
|
G | A | 1 | a0001c0002t0001g0302 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.5656-14917C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194619 | ||||||
| chr22:42194632
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5656-14930G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194632 | ||||||
| chr22:42194672
|
T | C | 5 | a0001c0002t0002g0132a0001c0002t0002g0138a0005c0009t0008g0353others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.5656-14970A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194672 | ||||||
| chr22:42194779
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5655+14872G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42194779 | ||||||
| chr22:42195447
|
C | T | 1 | a0001c0002t0001g0277 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.5655+14204G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195447 | ||||||
| chr22:42195586
|
C | T | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5655+14065G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195586 | ||||||
| chr22:42195593
|
C | T | 3 | a0001c0006t0002g0246a0001c0006t0002g0247a0001c0006t0002g0250 | 3 | HG01884.hp2 HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.5655+14058G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195593 | ||||||
| chr22:42195702
|
G | A | 1 | a0001c0012t0002g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5655+13949C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195702 | ||||||
| chr22:42195722
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5655+13929T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195722 | ||||||
| chr22:42195866
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5655+13785C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195866 | ||||||
| chr22:42195928
|
T | TCA | 17 | a0001c0001t0001g0267a0001c0001t0002g0096a0001c0001t0002g0344others(14): Show | 17 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.5655+13721_5655+13 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195928 | ||||||
| chr22:42195937
|
A | G | 1 | a0001c0001t0016g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5655+13714T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42195937 | ||||||
| chr22:42196151
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5655+13500G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196151 | ||||||
| chr22:42196233
|
C | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.5655+13418G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196233 | ||||||
| chr22:42196253
|
C | T | 1 | a0003c0004t0001g0117 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5655+13398G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196253 | ||||||
| chr22:42196470
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.5655+13181G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196470 | ||||||
| chr22:42196570
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.5655+13081T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196570 | ||||||
| chr22:42196600
|
C | G | 11 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5655+13051G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196600 | ||||||
| chr22:42196754
|
TGA | T | 71 | a0001c0001t0001g0273a0001c0002t0001g0278a0001c0002t0001g0280others(68): Show | 71 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.5655+12895_5655+12 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196754 | ||||||
| chr22:42196788
|
C | T | 1 | a0008c0024t0001g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5655+12863G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42196788 | ||||||
| chr22:42197035
|
T | C | 1 | a0002c0003t0001g0041 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.5655+12616A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197035 | ||||||
| chr22:42197065
|
G | C | 1 | a0006c0008t0001g0071 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5655+12586C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197065 | ||||||
| chr22:42197181
|
A | G | 1 | a0001c0002t0001g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.5655+12470T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197181 | ||||||
| chr22:42197322
|
C | CT | 54 | a0001c0001t0001g0006a0001c0001t0001g0116a0001c0001t0001g0137others(51): Show | 54 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.5655+12328dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197322 | ||||||
| chr22:42197322
|
CT | C | 11 | a0001c0001t0001g0154a0001c0001t0001g0251a0001c0002t0001g0329others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.5655+12328delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197322 | ||||||
| chr22:42197361
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5655+12290G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197361 | ||||||
| chr22:42197416
|
G | A | 1 | a0010c0014t0001g0352 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5655+12235C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197416 | ||||||
| chr22:42197471
|
C | T | 1 | a0001c0021t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5655+12180G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197471 | ||||||
| chr22:42197515
|
G | C | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(8): Show | 11 | HG00621.hp1 NA18747.hp2 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.5655+12136C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197515 | ||||||
| chr22:42197524
|
G | A | 1 | a0001c0010t0006g0008 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5655+12127C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197524 | ||||||
| chr22:42197564
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.5655+12087G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197564 | ||||||
| chr22:42197617
|
C | T | 4 | a0001c0002t0001g0294a0001c0002t0001g0295a0001c0002t0001g0296others(1): Show | 4 | HG02602.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.5655+12034G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197617 | ||||||
| chr22:42197693
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5655+11958G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197693 | ||||||
| chr22:42197825
|
C | T | 13 | a0001c0002t0001g0278a0001c0002t0001g0280a0001c0002t0001g0283others(10): Show | 13 | HG00597.hp2 HG00621.hp2 HG04184.hp2 others(10): Show |
intron_variant | MODIFIER | c.5655+11826G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197825 | ||||||
| chr22:42197944
|
T | C | 2 | a0001c0001t0001g0275a0001c0001t0004g0276 | 2 | NA18977.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.5655+11707A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197944 | ||||||
| chr22:42197959
|
G | C | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5655+11692C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42197959 | ||||||
| chr22:42198022
|
A | G | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5655+11629T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198022 | ||||||
| chr22:42198237
|
G | C | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5655+11414C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198237 | ||||||
| chr22:42198362
|
T | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+11289A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198362 | ||||||
| chr22:42198421
|
C | G | 3 | a0005c0009t0008g0353a0005c0009t0008g0355a0016c0029t0022g0354 | 3 | HG02572.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.5655+11230G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198421 | ||||||
| chr22:42198481
|
T | C | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5655+11170A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198481 | ||||||
| chr22:42198487
|
A | G | 1 | a0001c0002t0002g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5655+11164T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198487 | ||||||
| chr22:42198653
|
G | T | 1 | a0001c0002t0001g0297 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.5655+10998C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198653 | ||||||
| chr22:42198665
|
G | GT | 35 | a0001c0001t0001g0017a0001c0001t0001g0193a0001c0001t0001g0217others(32): Show | 35 | HG00621.hp1 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.5655+10985dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198665 | ||||||
| chr22:42198665
|
G | GTT | 78 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(75): Show | 78 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.5655+10984_5655+10 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198665 | ||||||
| chr22:42198829
|
T | A | 5 | a0001c0002t0002g0132a0001c0002t0002g0138a0005c0009t0008g0353others(2): Show | 5 | HG02559.hp1 HG02572.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.5655+10822A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198829 | ||||||
| chr22:42198945
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5655+10706C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198945 | ||||||
| chr22:42198970
|
C | A | 1 | a0002c0003t0001g0065 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.5655+10681G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42198970 | ||||||
| chr22:42199075
|
G | A | 3 | a0001c0001t0004g0095a0007c0011t0004g0244a0007c0011t0004g0254 | 3 | HG02486.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5655+10576C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199075 | ||||||
| chr22:42199167
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5655+10484G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199167 | ||||||
| chr22:42199252
|
G | C | 71 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.5655+10399C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199252 | ||||||
| chr22:42199341
|
C | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5655+10310G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199341 | ||||||
| chr22:42199462
|
CAG | C | 3 | a0001c0002t0001g0316a0001c0002t0001g0319a0001c0002t0001g0320 | 3 | NA18967.hp2 NA18981.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.5655+10187_5655+10 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199462 | ||||||
| chr22:42199673
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5655+9978G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199673 | ||||||
| chr22:42199706
|
C | CA | 80 | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0001g0139others(77): Show | 80 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.5655+9944dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199706
|
C | CAA | 33 | a0001c0001t0001g0017a0001c0001t0001g0137a0001c0001t0001g0143others(30): Show | 33 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.5655+9943_5655+994 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199706
|
C | CAAA | 16 | a0001c0001t0001g0153a0001c0001t0001g0170a0001c0001t0001g0202others(13): Show | 16 | HG00621.hp2 HG00733.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.5655+9942_5655+994 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199706
|
CA | C | 14 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0159others(11): Show | 14 | HG00323.hp1 HG01069.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.5655+9944delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199706
|
CAA | C | 31 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0094others(28): Show | 31 | HG01433.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.5655+9943_5655+994 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199706
|
CAAA | C | 46 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(43): Show | 46 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5655+9942_5655+994 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199706
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0003t0001g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.5655+9935_5655+994 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199706
|
CAAAAAAA others(9): Show |
C | 1 | a0006c0008t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5655+9929_5655+994 others(20): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199706 | ||||||
| chr22:42199781
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0015g0337 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5655+9870G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199781 | ||||||
| chr22:42199844
|
C | CA | 21 | a0001c0001t0001g0154a0001c0001t0001g0192a0001c0001t0001g0245others(18): Show | 21 | HG01433.hp2 HG01884.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.5655+9806dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199844 | ||||||
| chr22:42199920
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0016g0147 | 3 | HG01192.hp2 HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.5655+9731T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199920 | ||||||
| chr22:42199966
|
T | TTTTC | 257 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(254): Show | 257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.5655+9684_5655+968 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42199966 | ||||||
| chr22:42200139
|
T | C | 1 | a0002c0003t0001g0044 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.5655+9512A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200139 | ||||||
| chr22:42200171
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5655+9480G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200171 | ||||||
| chr22:42200247
|
C | A | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.5655+9404G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200247 | ||||||
| chr22:42200274
|
G | A | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+9377C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200274 | ||||||
| chr22:42200368
|
C | T | 1 | a0001c0002t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5655+9283G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200368 | ||||||
| chr22:42200403
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5655+9248A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200403 | ||||||
| chr22:42200420
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5655+9231G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200420 | ||||||
| chr22:42200451
|
G | C | 1 | a0002c0003t0017g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5655+9200C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200451 | ||||||
| chr22:42200572
|
G | A | 1 | a0001c0001t0016g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5655+9079C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200572 | ||||||
| chr22:42200590
|
C | T | 6 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.5655+9061G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200590 | ||||||
| chr22:42200635
|
T | C | 66 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(63): Show | 66 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.5655+9016A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200635 | ||||||
| chr22:42200641
|
C | CA | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.5655+9009dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200641 | ||||||
| chr22:42200641
|
C | CAA | 45 | a0001c0001t0001g0007a0001c0001t0001g0143a0001c0001t0001g0149others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.5655+9008_5655+900 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200641 | ||||||
| chr22:42200875
|
A | G | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5655+8776T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42200875 | ||||||
| chr22:42201302
|
A | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5655+8349T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42201302 | ||||||
| chr22:42201372
|
G | T | 2 | a0001c0001t0001g0149a0001c0017t0001g0150 | 2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.5655+8279C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42201372 | ||||||
| chr22:42201418
|
G | C | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+8233C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42201418 | ||||||
| chr22:42201440
|
T | G | 1 | a0001c0001t0001g0006 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.5655+8211A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42201440 | ||||||
| chr22:42201716
|
C | T | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+7935G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42201716 | ||||||
| chr22:42201830
|
C | G | 265 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(262): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.5655+7821G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42201830 | ||||||
| chr22:42202236
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.5655+7415A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202236 | ||||||
| chr22:42202301
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5655+7350T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202301 | ||||||
| chr22:42202525
|
T | C | 1 | a0002c0003t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.5655+7126A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202525 | ||||||
| chr22:42202526
|
C | T | 1 | a0002c0003t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.5655+7125G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202526 | ||||||
| chr22:42202532
|
T | C | 26 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0106others(23): Show | 26 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.5655+7119A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202532 | ||||||
| chr22:42202553
|
G | T | 2 | a0001c0001t0001g0267a0001c0012t0002g0231 | 2 | HG02258.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5655+7098C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202553 | ||||||
| chr22:42202601
|
C | T | 16 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0012t0002g0231others(13): Show | 16 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.5655+7050G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202601 | ||||||
| chr22:42202612
|
C | G | 1 | a0001c0001t0001g0197 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5655+7039G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202612 | ||||||
| chr22:42202644
|
G | A | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5655+7007C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202644 | ||||||
| chr22:42202668
|
G | A | 1 | a0001c0002t0001g0290 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5655+6983C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202668 | ||||||
| chr22:42202945
|
T | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.5655+6706A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42202945 | ||||||
| chr22:42203060
|
G | A | 4 | a0001c0001t0001g0154a0001c0001t0005g0152a0001c0001t0005g0182others(1): Show | 4 | NA18961.hp1 NA19004.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.5655+6591C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203060 | ||||||
| chr22:42203092
|
T | C | 1 | a0001c0021t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5655+6559A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203092 | ||||||
| chr22:42203218
|
G | A | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5655+6433C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203218 | ||||||
| chr22:42203304
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5655+6347G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203304 | ||||||
| chr22:42203440
|
T | C | 55 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(52): Show | 55 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.5655+6211A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203440 | ||||||
| chr22:42203466
|
G | A | 1 | a0001c0002t0001g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5655+6185C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203466 | ||||||
| chr22:42203547
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5655+6104G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203547 | ||||||
| chr22:42203641
|
G | C | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.5655+6010C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203641 | ||||||
| chr22:42203648
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5655+6003G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203648 | ||||||
| chr22:42203976
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5655+5675C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203976 | ||||||
| chr22:42203992
|
A | G | 1 | a0001c0001t0004g0276 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.5655+5659T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42203992 | ||||||
| chr22:42204061
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5655+5590A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204061 | ||||||
| chr22:42204247
|
T | C | 1 | a0001c0002t0001g0266 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5655+5404A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204247 | ||||||
| chr22:42204336
|
A | C | 1 | a0001c0001t0001g0134 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.5655+5315T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204336 | ||||||
| chr22:42204514
|
A | C | 1 | a0003c0004t0001g0117 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5655+5137T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204514 | ||||||
| chr22:42204583
|
G | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.5655+5068C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204583 | ||||||
| chr22:42204592
|
C | A | 1 | a0001c0012t0002g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.5655+5059G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204592 | ||||||
| chr22:42204631
|
G | GATCAGGA others(6): Show |
1 | a0001c0001t0001g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5655+5007_5655+501 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204631 | ||||||
| chr22:42204772
|
G | A | 2 | a0001c0002t0001g0339a0011c0020t0001g0340 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5655+4879C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204772 | ||||||
| chr22:42204892
|
A | G | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5655+4759T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204892 | ||||||
| chr22:42204905
|
T | TA | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+4745dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204905 | ||||||
| chr22:42204905
|
TA | T | 58 | a0001c0001t0002g0344a0002c0003t0001g0010a0002c0003t0001g0020others(55): Show | 58 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.5655+4745delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204905 | ||||||
| chr22:42204995
|
G | A | 4 | a0001c0002t0001g0294a0001c0002t0001g0295a0001c0002t0001g0296others(1): Show | 4 | HG02602.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.5655+4656C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42204995 | ||||||
| chr22:42205084
|
C | T | 1 | a0003c0004t0001g0117 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5655+4567G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205084 | ||||||
| chr22:42205117
|
G | A | 1 | a0003c0027t0001g0124 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5655+4534C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205117 | ||||||
| chr22:42205208
|
A | C | 1 | a0001c0028t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5655+4443T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205208 | ||||||
| chr22:42205280
|
T | A | 1 | a0001c0022t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5655+4371A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205280 | ||||||
| chr22:42205283
|
G | GGGAAGGG others(5): Show |
14 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(11): Show | 14 | HG00738.hp1 HG01074.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.5655+4356_5655+436 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205283 | ||||||
| chr22:42205283
|
G | GGGAAGGG others(17): Show |
50 | a0001c0001t0003g0011a0002c0003t0001g0010a0002c0003t0001g0020others(47): Show | 50 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.5655+4344_5655+436 others(28): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205283 | ||||||
| chr22:42205283
|
G | GGGAAGGG others(29): Show |
1 | a0002c0003t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5655+4367_5655+436 others(40): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205283 | ||||||
| chr22:42205283
|
GGGAAGGG others(5): Show |
G | 20 | a0001c0002t0001g0287a0003c0004t0001g0107a0003c0004t0001g0108others(17): Show | 20 | HG00639.hp1 HG01243.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.5655+4356_5655+436 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205283 | ||||||
| chr22:42205565
|
T | G | 1 | a0001c0001t0016g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5655+4086A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205565 | ||||||
| chr22:42205720
|
G | A | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.5655+3931C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205720 | ||||||
| chr22:42205898
|
A | C | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.5655+3753T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205898 | ||||||
| chr22:42205899
|
G | A | 1 | a0004c0005t0002g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5655+3752C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205899 | ||||||
| chr22:42205914
|
G | C | 1 | a0003c0004t0003g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5655+3737C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205914 | ||||||
| chr22:42205918
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5655+3733G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205918 | ||||||
| chr22:42205935
|
C | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0184others(1): Show | 4 | NA18940.hp1 NA18967.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.5655+3716G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42205935 | ||||||
| chr22:42206133
|
C | T | 157 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.5655+3518G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206133 | ||||||
| chr22:42206418
|
C | G | 1 | a0001c0002t0001g0280 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5655+3233G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206418 | ||||||
| chr22:42206478
|
CTTTGACA others(4): Show |
C | 28 | a0001c0001t0001g0267a0001c0001t0002g0091a0001c0001t0002g0092others(25): Show | 28 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.5655+3162_5655+317 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206478 | ||||||
| chr22:42206490
|
G | A | 28 | a0001c0001t0001g0267a0001c0001t0002g0091a0001c0001t0002g0092others(25): Show | 28 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.5655+3161C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206490 | ||||||
| chr22:42206514
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.5655+3137C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206514 | ||||||
| chr22:42206642
|
G | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+3009C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206642 | ||||||
| chr22:42206652
|
G | A | 2 | a0002c0003t0001g0024a0002c0003t0001g0027 | 2 | HG00733.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.5655+2999C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206652 | ||||||
| chr22:42206675
|
G | C | 1 | a0004c0005t0002g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5655+2976C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206675 | ||||||
| chr22:42206698
|
G | A | 57 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(54): Show | 57 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.5655+2953C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206698 | ||||||
| chr22:42206953
|
A | G | 55 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(52): Show | 55 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.5655+2698T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42206953 | ||||||
| chr22:42207242
|
A | G | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.5655+2409T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207242 | ||||||
| chr22:42207363
|
G | GT | 9 | a0001c0001t0001g0192a0001c0002t0001g0290a0001c0002t0002g0138others(6): Show | 9 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+2287dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207363 | ||||||
| chr22:42207435
|
C | T | 1 | a0001c0021t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5655+2216G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207435 | ||||||
| chr22:42207464
|
C | A | 1 | a0001c0002t0001g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5655+2187G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207464 | ||||||
| chr22:42207540
|
G | C | 1 | a0001c0002t0001g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5655+2111C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207540 | ||||||
| chr22:42207582
|
G | A | 2 | a0001c0001t0013g0114a0002c0003t0001g0079 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5655+2069C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207582 | ||||||
| chr22:42207642
|
C | G | 1 | a0002c0003t0001g0036 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5655+2009G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207642 | ||||||
| chr22:42207808
|
C | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 212 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.5655+1843G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207808 | ||||||
| chr22:42207863
|
G | A | 53 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(50): Show | 53 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.5655+1788C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42207863 | ||||||
| chr22:42208368
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5655+1283A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42208368 | ||||||
| chr22:42208452
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0012others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.5655+1199G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42208452 | ||||||
| chr22:42208536
|
G | A | 2 | a0001c0001t0002g0344a0005c0009t0001g0089 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5655+1115C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42208536 | ||||||
| chr22:42208584
|
CAACAAAA others(3): Show |
C | 1 | a0001c0001t0003g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5655+1057_5655+106 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42208584 | ||||||
| chr22:42208701
|
A | G | 1 | a0002c0003t0001g0036 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5655+950T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42208701 | ||||||
| chr22:42208818
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.5655+833A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42208818 | ||||||
| chr22:42208879
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0130a0001c0001t0001g0166others(5): Show | 8 | HG00621.hp1 NA18747.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.5655+772G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42208879 | ||||||
| chr22:42209239
|
G | C | 1 | a0001c0002t0001g0325 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.5655+412C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42209239 | ||||||
| chr22:42209487
|
T | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.5655+164A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42209487 | ||||||
| chr22:42209536
|
C | T | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.5655+115G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42209536 | ||||||
| chr22:42209542
|
C | T | 54 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(51): Show | 54 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.5655+109G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 2/5 | chr22 | 42209542 | ||||||
| chr22:42215374
|
G | A | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-33C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42215374 | ||||||
| chr22:42215467
|
A | AT | 19 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0002t0001g0336others(16): Show | 19 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-36-127dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42215467 | ||||||
| chr22:42215782
|
C | A | 6 | a0001c0002t0001g0271a0001c0002t0001g0288a0001c0002t0001g0321others(3): Show | 6 | HG00735.hp2 HG01074.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-441G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42215782 | ||||||
| chr22:42215828
|
G | C | 25 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0106others(22): Show | 25 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-36-487C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42215828 | ||||||
| chr22:42216045
|
G | A | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-704C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216045 | ||||||
| chr22:42216048
|
G | A | 1 | a0006c0008t0001g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-36-707C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216048 | ||||||
| chr22:42216073
|
C | G | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-36-732G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216073 | ||||||
| chr22:42216079
|
C | CT | 71 | a0001c0001t0001g0267a0001c0001t0001g0273a0001c0001t0001g0293others(68): Show | 71 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-36-739dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTT | 15 | a0001c0001t0001g0208a0001c0001t0001g0252a0001c0002t0018g0261others(12): Show | 15 | HG00544.hp1 HG00639.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-740_-36-739dup others(2): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTT | 26 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0253others(23): Show | 26 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-36-741_-36-739dup others(3): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTT | 9 | a0001c0001t0002g0014a0001c0001t0002g0094a0001c0010t0006g0009others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-742_-36-739dup others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(1): Show |
23 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0148others(20): Show | 23 | HG00280.hp2 HG00558.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-36-746_-36-739dup others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(2): Show |
28 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0140others(25): Show | 28 | HG00099.hp1 HG01192.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.-36-747_-36-739dup others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(3): Show |
23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 23 | HG00140.hp1 HG00673.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-36-748_-36-739dup others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(4): Show |
18 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0130others(15): Show | 18 | HG00544.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36-749_-36-739dup others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(5): Show |
10 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0101others(7): Show | 10 | HG00621.hp1 HG01109.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-36-750_-36-739dup others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0134a0001c0001t0010g0002a0001c0002t0007g0103 | 3 | HG02622.hp2 NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-36-751_-36-739dup others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(7): Show |
2 | a0001c0002t0007g0102a0005c0009t0001g0089 | 2 | HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-752_-36-739dup others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0194a0001c0001t0001g0209 | 2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-36-753_-36-739dup others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0160a0003c0004t0001g0110 | 2 | HG01243.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-36-755_-36-739dup others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(18): Show |
3 | a0003c0004t0001g0111a0003c0004t0001g0112a0003c0004t0001g0120 | 3 | HG01070.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-36-763_-36-739dup others(25): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(19): Show |
3 | a0003c0004t0001g0109a0003c0004t0001g0119a0003c0004t0003g0126 | 3 | HG01071.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-36-764_-36-739dup others(26): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(20): Show |
1 | a0003c0004t0003g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-36-765_-36-739dup others(27): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(23): Show |
1 | a0003c0004t0003g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-36-739_-36-738ins others(30): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(24): Show |
1 | a0003c0004t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-36-739_-36-738ins others(31): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
C | CTTTTTTT others(25): Show |
1 | a0003c0004t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-36-739_-36-738ins others(32): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0226a0001c0001t0001g0245a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-746_-36-739del others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
CTTTTTTT others(4): Show |
C | 1 | a0003c0004t0001g0115 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-36-749_-36-739del others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216079
|
CTTTTTTT others(6): Show |
C | 1 | a0003c0004t0001g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-36-751_-36-739del others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216079 | ||||||
| chr22:42216290
|
C | T | 12 | a0001c0002t0001g0256a0001c0002t0001g0260a0001c0002t0001g0271others(9): Show | 12 | HG00099.hp2 HG00735.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-949G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216290 | ||||||
| chr22:42216291
|
G | A | 27 | a0001c0001t0001g0116a0001c0001t0013g0114a0003c0004t0001g0104others(24): Show | 27 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-36-950C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216291 | ||||||
| chr22:42216354
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0164 | 2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.-36-1013G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216354 | ||||||
| chr22:42216402
|
T | C | 73 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-1061A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216402 | ||||||
| chr22:42216551
|
A | G | 2 | a0001c0001t0002g0344a0005c0009t0001g0089 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-1210T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42216551 | ||||||
| chr22:42217184
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36-1843G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42217184 | ||||||
| chr22:42217199
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36-1858C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42217199 | ||||||
| chr22:42217209
|
T | C | 1 | a0001c0002t0001g0315 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-36-1868A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42217209 | ||||||
| chr22:42217237
|
G | A | 9 | a0002c0003t0001g0052a0002c0003t0001g0053a0002c0003t0001g0054others(6): Show | 9 | HG00738.hp1 HG01074.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.-36-1896C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42217237 | ||||||
| chr22:42217479
|
G | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-36-2138C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42217479 | ||||||
| chr22:42217665
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36-2324A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42217665 | ||||||
| chr22:42217679
|
A | C | 1 | a0001c0002t0001g0342 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-36-2338T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42217679 | ||||||
| chr22:42218220
|
G | A | 2 | a0001c0001t0002g0344a0005c0009t0001g0089 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-36-2879C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42218220 | ||||||
| chr22:42218273
|
A | G | 1 | a0011c0020t0001g0340 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-36-2932T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42218273 | ||||||
| chr22:42218356
|
T | C | 112 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0002g0096others(109): Show | 112 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.-36-3015A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42218356 | ||||||
| chr22:42218395
|
G | C | 227 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.-36-3054C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42218395 | ||||||
| chr22:42218789
|
C | A | 3 | a0005c0009t0008g0353a0005c0009t0008g0355a0016c0029t0022g0354 | 3 | HG02572.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-36-3448G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42218789 | ||||||
| chr22:42218817
|
C | CTGT | 73 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-3479_-36-3477d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42218817 | ||||||
| chr22:42218898
|
GA | G | 82 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0012others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-36-3558delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42218898 | ||||||
| chr22:42219042
|
AACCAACT others(3): Show |
A | 1 | a0001c0002t0001g0097 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-36-3711_-36-3702d others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219042 | ||||||
| chr22:42219048
|
C | G | 255 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.-36-3707G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219048 | ||||||
| chr22:42219054
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36-3713A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219054 | ||||||
| chr22:42219163
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-36-3822G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219163 | ||||||
| chr22:42219164
|
G | C | 1 | a0001c0022t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-36-3823C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219164 | ||||||
| chr22:42219229
|
G | A | 1 | a0001c0002t0001g0299 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-36-3888C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219229 | ||||||
| chr22:42219355
|
C | CA | 22 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(19): Show | 22 | HG01192.hp2 HG01516.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36-4015dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAA | 14 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(11): Show | 14 | HG01243.hp2 HG02109.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-4016_-36-4015d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAA | 8 | a0001c0001t0001g0161a0001c0001t0001g0186a0001c0002t0001g0336others(5): Show | 8 | HG01074.hp1 HG02145.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36-4017_-36-4015d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAA | 6 | a0001c0001t0001g0149a0001c0001t0001g0163a0001c0001t0001g0204others(3): Show | 6 | HG00558.hp2 HG00733.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-4020_-36-4015d others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0116a0001c0001t0003g0015a0004c0005t0002g0235 | 3 | HG02145.hp2 HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-36-4024_-36-4015d others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(4): Show |
11 | a0001c0001t0001g0135a0001c0001t0003g0016a0001c0001t0005g0152others(8): Show | 11 | HG01891.hp1 HG02451.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36-4025_-36-4015d others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0017a0001c0001t0001g0267a0001c0001t0002g0344others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-4026_-36-4015d others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0137a0001c0001t0001g0223a0001c0001t0002g0350others(5): Show | 8 | HG00639.hp1 HG01346.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36-4027_-36-4015d others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0002g0248a0001c0006t0002g0247a0003c0004t0001g0108others(1): Show | 4 | HG01884.hp2 HG02055.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-4028_-36-4015d others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0188a0003c0004t0001g0109a0003c0004t0001g0110others(1): Show | 4 | HG00741.hp1 HG01243.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-4029_-36-4015d others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-36-4030_-36-4015d others(18): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0202a0001c0001t0001g0203a0003c0004t0001g0111 | 3 | HG02615.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-36-4031_-36-4015d others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0136a0001c0002t0002g0132a0001c0028t0001g0133 | 3 | HG00544.hp2 HG03486.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-36-4032_-36-4015d others(20): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0190a0001c0001t0001g0201a0001c0001t0001g0216 | 3 | HG01256.hp2 HG01891.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-36-4033_-36-4015d others(21): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(13): Show |
9 | a0001c0001t0001g0004a0001c0001t0001g0170a0001c0001t0001g0207others(6): Show | 9 | HG00639.hp2 HG01261.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-4034_-36-4015d others(22): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(14): Show |
11 | a0001c0001t0001g0006a0001c0001t0001g0153a0001c0001t0001g0159others(8): Show | 11 | HG00642.hp2 HG01070.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.-36-4035_-36-4015d others(23): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(15): Show |
10 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG00621.hp1 HG00738.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36-4036_-36-4015d others(24): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(16): Show |
4 | a0001c0001t0001g0134a0001c0001t0001g0179a0001c0001t0013g0114others(1): Show | 4 | HG00099.hp1 HG02976.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-4037_-36-4015d others(25): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(17): Show |
4 | a0001c0001t0001g0140a0001c0001t0001g0171a0003c0004t0001g0105others(1): Show | 4 | HG01099.hp1 HG01255.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-4038_-36-4015d others(26): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0194 | 2 | HG01261.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-36-4039_-36-4015d others(27): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(19): Show |
5 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0181others(2): Show | 5 | HG00280.hp2 HG02559.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-4040_-36-4015d others(28): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(20): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0175others(7): Show | 10 | HG00673.hp2 HG01928.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(29): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(21): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0199others(1): Show | 4 | HG00140.hp1 HG01069.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(30): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0001g0227a0003c0004t0001g0119 | 2 | HG01071.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(31): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(23): Show |
2 | a0001c0001t0001g0142a0003c0004t0001g0120 | 2 | HG01070.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(32): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0151 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(33): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0139a0001c0001t0001g0154 | 2 | NA19004.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(34): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(27): Show |
3 | a0001c0001t0001g0169a0001c0001t0001g0221a0003c0004t0001g0118 | 3 | HG03490.hp1 NA18994.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(36): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(28): Show |
2 | a0001c0001t0001g0178a0003c0004t0001g0123 | 2 | HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(37): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0172 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(38): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0174 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(39): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(31): Show |
1 | a0001c0001t0001g0196 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(40): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0002g0173 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(41): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(33): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0185 | 2 | HG03239.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-36-4015_-36-4014i others(42): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(37): Show |
1 | a0001c0001t0001g0198 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(46): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(40): Show |
1 | a0003c0004t0001g0128 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(49): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(46): Show |
1 | a0001c0001t0001g0143 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(55): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
C | CAAAAAAA others(47): Show |
1 | a0001c0001t0001g0189 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-36-4015_-36-4014i others(56): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
CAAAAAAA others(3): Show |
C | 70 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(67): Show | 70 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-36-4024_-36-4015d others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219355
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0003t0001g0047 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-36-4025_-36-4015d others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219355 | ||||||
| chr22:42219478
|
A | G | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-4137T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219478 | ||||||
| chr22:42219486
|
T | G | 3 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0351 | 3 | HG01099.hp1 HG01261.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-36-4145A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219486 | ||||||
| chr22:42219665
|
G | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-36-4324C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219665 | ||||||
| chr22:42219676
|
C | T | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-36-4335G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219676 | ||||||
| chr22:42219765
|
A | G | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-36-4424T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219765 | ||||||
| chr22:42219791
|
G | C | 1 | a0001c0001t0003g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-36-4450C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219791 | ||||||
| chr22:42219901
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36-4560T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42219901 | ||||||
| chr22:42220070
|
A | G | 3 | a0001c0002t0001g0272a0001c0002t0001g0284a0001c0002t0001g0285 | 3 | NA18939.hp2 NA18973.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-36-4729T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220070 | ||||||
| chr22:42220114
|
A | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-4773T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220114 | ||||||
| chr22:42220147
|
G | A | 5 | a0001c0002t0001g0303a0001c0002t0001g0323a0001c0002t0001g0325others(2): Show | 5 | NA18966.hp2 NA19004.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-4806C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220147 | ||||||
| chr22:42220166
|
C | T | 3 | a0006c0008t0001g0028a0006c0008t0001g0071a0006c0008t0001g0080 | 3 | HG03704.hp1 HG04228.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-36-4825G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220166 | ||||||
| chr22:42220189
|
AAG | A | 16 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0012t0002g0231others(13): Show | 16 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-36-4850_-36-4849d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220189 | ||||||
| chr22:42220209
|
C | T | 16 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0012t0002g0231others(13): Show | 16 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-36-4868G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220209 | ||||||
| chr22:42220274
|
C | G | 17 | a0002c0003t0001g0020a0002c0003t0001g0021a0002c0003t0001g0038others(14): Show | 17 | HG02015.hp1 HG02027.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-36-4933G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220274 | ||||||
| chr22:42220449
|
C | T | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-5108G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220449 | ||||||
| chr22:42220507
|
C | T | 1 | a0002c0003t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-36-5166G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220507 | ||||||
| chr22:42220907
|
T | G | 1 | a0002c0003t0001g0020 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-36-5566A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42220907 | ||||||
| chr22:42221009
|
A | G | 16 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0012t0002g0231others(13): Show | 16 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-36-5668T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221009 | ||||||
| chr22:42221126
|
A | C | 1 | a0001c0002t0001g0299 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-36-5785T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221126 | ||||||
| chr22:42221171
|
T | C | 81 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(78): Show | 81 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-36-5830A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221171 | ||||||
| chr22:42221405
|
T | C | 81 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(78): Show | 81 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-36-6064A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221405 | ||||||
| chr22:42221450
|
T | C | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-6109A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221450 | ||||||
| chr22:42221456
|
A | G | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-6115T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221456 | ||||||
| chr22:42221739
|
G | GT | 14 | a0001c0001t0001g0273a0001c0002t0001g0255a0001c0002t0001g0265others(11): Show | 14 | HG00438.hp1 HG00741.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-6399dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(2): Show |
14 | a0001c0001t0001g0136a0001c0001t0001g0144a0001c0001t0001g0151others(11): Show | 14 | HG00544.hp2 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-36-6407_-36-6399d others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(3): Show |
79 | a0001c0001t0001g0004a0001c0001t0001g0135a0001c0001t0001g0140others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.-36-6408_-36-6399d others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(4): Show |
93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-36-6409_-36-6399d others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(5): Show |
42 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0100others(39): Show | 42 | HG00735.hp1 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.-36-6410_-36-6399d others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(6): Show |
28 | a0001c0001t0001g0116a0001c0001t0002g0350a0001c0002t0007g0102others(25): Show | 28 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-36-6411_-36-6399d others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(7): Show |
12 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0091others(9): Show | 12 | HG00544.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36-6412_-36-6399d others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0002g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-36-6413_-36-6399d others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221739
|
G | GTTTTTTT others(9): Show |
2 | a0001c0010t0006g0009a0012c0018t0002g0243 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-36-6414_-36-6399d others(18): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221739 | ||||||
| chr22:42221741
|
T | TTTTTTTT others(3): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0188 | 2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-36-6401_-36-6400i others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221741 | ||||||
| chr22:42221844
|
T | C | 1 | a0008c0024t0001g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-36-6503A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42221844 | ||||||
| chr22:42222028
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-36-6687C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222028 | ||||||
| chr22:42222330
|
A | ATGCTACC others(1161): Show |
1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-8157_-36-6990d others(1170): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222330 | ||||||
| chr22:42222334
|
T | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-36-6993A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222334 | ||||||
| chr22:42222344
|
T | C | 2 | a0003c0004t0001g0104a0003c0004t0001g0105 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-36-7003A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222344 | ||||||
| chr22:42222346
|
A | C | 10 | a0002c0003t0001g0018a0002c0003t0001g0022a0002c0003t0001g0029others(7): Show | 10 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36-7005T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222346 | ||||||
| chr22:42222473
|
T | A | 25 | a0001c0001t0001g0267a0001c0001t0002g0091a0001c0001t0002g0092others(22): Show | 25 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.-36-7132A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222473 | ||||||
| chr22:42222488
|
A | AC | 16 | a0002c0003t0001g0018a0002c0003t0001g0022a0002c0003t0001g0023others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.-36-7148dupG | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222488 | ||||||
| chr22:42222656
|
C | T | 4 | a0001c0002t0001g0307a0001c0002t0001g0308a0001c0002t0001g0313others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-7315G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222656 | ||||||
| chr22:42222663
|
A | G | 75 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(72): Show | 75 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-36-7322T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222663 | ||||||
| chr22:42222974
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0012others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-7633G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222974 | ||||||
| chr22:42222983
|
C | T | 1 | a0001c0010t0006g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-36-7642G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42222983 | ||||||
| chr22:42223061
|
A | G | 75 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(72): Show | 75 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-36-7720T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42223061 | ||||||
| chr22:42223302
|
A | G | 73 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-7961T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42223302 | ||||||
| chr22:42223835
|
A | G | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-8494T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42223835 | ||||||
| chr22:42224209
|
C | T | 1 | a0015c0013t0001g0059 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-36-8868G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224209 | ||||||
| chr22:42224413
|
A | G | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-9072T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224413 | ||||||
| chr22:42224476
|
T | A | 4 | a0003c0004t0003g0121a0003c0004t0003g0125a0003c0004t0003g0126others(1): Show | 4 | HG02486.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-9135A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224476 | ||||||
| chr22:42224492
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-9151T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224492 | ||||||
| chr22:42224534
|
C | CA | 50 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0264others(47): Show | 50 | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.-36-9194dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
C | CAA | 15 | a0001c0001t0001g0263a0001c0001t0001g0275a0001c0002t0001g0308others(12): Show | 15 | HG01071.hp2 HG01109.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-9195_-36-9194d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
C | CAAA | 14 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0106others(11): Show | 14 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-9196_-36-9194d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
C | CAAAA | 6 | a0003c0004t0001g0108a0003c0004t0001g0111a0003c0004t0001g0112others(3): Show | 6 | HG01167.hp2 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-9197_-36-9194d others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
CA | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0098others(55): Show | 58 | HG00280.hp2 HG00642.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.-36-9194delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
CAA | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-36-9195_-36-9194d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0002t0001g0265a0001c0002t0001g0266a0001c0002t0001g0269 | 3 | HG01099.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-36-9204_-36-9194d others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
CAAAAAAA others(6): Show |
C | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-9206_-36-9194d others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224534
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0139a0001c0001t0002g0096 | 2 | HG03516.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-36-9208_-36-9194d others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224534 | ||||||
| chr22:42224540
|
A | G | 4 | a0001c0002t0001g0303a0001c0002t0001g0323a0001c0002t0001g0325others(1): Show | 4 | NA18966.hp2 NA19004.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-9199T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224540 | ||||||
| chr22:42224544
|
A | G | 1 | a0001c0002t0011g0003 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-36-9203T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224544 | ||||||
| chr22:42224789
|
A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.-36-9448T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224789 | ||||||
| chr22:42224796
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-36-9455G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224796 | ||||||
| chr22:42224822
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-9481G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224822 | ||||||
| chr22:42224934
|
T | C | 108 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(105): Show | 108 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-36-9593A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224934 | ||||||
| chr22:42224935
|
G | A | 2 | a0003c0004t0001g0128a0007c0011t0004g0244 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-9594C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42224935 | ||||||
| chr22:42225000
|
C | CT | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-36-9660dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225000 | ||||||
| chr22:42225000
|
C | CTT | 97 | a0001c0001t0001g0017a0001c0001t0001g0116a0001c0001t0001g0130others(94): Show | 97 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-36-9661_-36-9660d others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225000 | ||||||
| chr22:42225000
|
C | CTTT | 7 | a0002c0003t0001g0082a0003c0004t0001g0104a0003c0004t0001g0105others(4): Show | 7 | HG00639.hp1 HG01099.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-36-9662_-36-9660d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225000 | ||||||
| chr22:42225000
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36-9659G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225000 | ||||||
| chr22:42225000
|
CT | C | 22 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0264others(19): Show | 22 | HG01175.hp1 HG01884.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-36-9660delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225000 | ||||||
| chr22:42225156
|
C | T | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-36-9815G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225156 | ||||||
| chr22:42225222
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG01070.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-36-9881G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225222 | ||||||
| chr22:42225226
|
C | T | 2 | a0001c0002t0001g0268a0001c0002t0001g0270 | 2 | HG00280.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-36-9885G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225226 | ||||||
| chr22:42225342
|
C | G | 1 | a0001c0002t0001g0302 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-36-10001G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225342 | ||||||
| chr22:42225353
|
A | G | 1 | a0002c0003t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-36-10012T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225353 | ||||||
| chr22:42225474
|
C | T | 1 | a0003c0004t0001g0128 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-36-10133G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225474 | ||||||
| chr22:42225584
|
G | A | 4 | a0001c0001t0001g0207a0001c0001t0001g0209a0001c0001t0001g0211others(1): Show | 4 | HG00642.hp2 HG01256.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-10243C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225584 | ||||||
| chr22:42225616
|
G | A | 18 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0267others(15): Show | 18 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36-10275C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225616 | ||||||
| chr22:42225620
|
C | CA | 42 | a0001c0001t0001g0161a0001c0001t0005g0183a0001c0002t0001g0299others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.-36-10280dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225620 | ||||||
| chr22:42225620
|
C | CAA | 36 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(33): Show | 36 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-36-10281_-36-1028 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225620 | ||||||
| chr22:42225620
|
CA | C | 35 | a0001c0001t0001g0017a0001c0001t0001g0146a0001c0001t0001g0153others(32): Show | 35 | HG01167.hp2 HG01192.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-36-10280delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225620 | ||||||
| chr22:42225637
|
A | T | 3 | a0001c0001t0001g0135a0001c0021t0001g0200a0001c0022t0001g0162 | 3 | HG02602.hp1 HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-36-10296T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225637 | ||||||
| chr22:42225659
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-36-10318T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225659 | ||||||
| chr22:42225766
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0170 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-36-10425C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225766 | ||||||
| chr22:42225986
|
C | T | 1 | a0003c0004t0001g0104 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-36-10645G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225986 | ||||||
| chr22:42225997
|
C | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.-36-10656G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42225997 | ||||||
| chr22:42226000
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0251 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-36-10659G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226000 | ||||||
| chr22:42226014
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-36-10673T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226014 | ||||||
| chr22:42226244
|
T | G | 1 | a0002c0003t0001g0030 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-36-10903A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226244 | ||||||
| chr22:42226306
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-36-10965C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226306 | ||||||
| chr22:42226363
|
T | C | 2 | a0001c0001t0001g0149a0001c0017t0001g0150 | 2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-36-11022A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226363 | ||||||
| chr22:42226424
|
C | T | 1 | a0009c0025t0001g0019 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-36-11083G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226424 | ||||||
| chr22:42226573
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-36-11232G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226573 | ||||||
| chr22:42226775
|
C | T | 3 | a0006c0008t0001g0028a0006c0008t0001g0071a0006c0008t0001g0080 | 3 | HG03704.hp1 HG04228.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-36-11434G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226775 | ||||||
| chr22:42226807
|
T | C | 3 | a0001c0001t0004g0095a0007c0011t0004g0244a0007c0011t0004g0254 | 3 | HG02486.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-11466A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226807 | ||||||
| chr22:42226909
|
T | C | 33 | a0001c0001t0001g0017a0001c0001t0001g0267a0001c0001t0002g0014others(30): Show | 33 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-36-11568A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226909 | ||||||
| chr22:42226945
|
A | C | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-36-11604T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42226945 | ||||||
| chr22:42227111
|
C | T | 1 | a0001c0016t0001g0311 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-36-11770G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227111 | ||||||
| chr22:42227202
|
G | C | 1 | a0008c0024t0001g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-36-11861C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227202 | ||||||
| chr22:42227207
|
C | A | 6 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-11866G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227207 | ||||||
| chr22:42227252
|
G | A | 73 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-11911C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227252 | ||||||
| chr22:42227510
|
T | A | 1 | a0001c0001t0013g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-36-12169A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227510 | ||||||
| chr22:42227712
|
C | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-36-12371G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227712 | ||||||
| chr22:42227767
|
A | G | 355 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(352): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-36-12426T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227767 | ||||||
| chr22:42227917
|
T | A | 1 | a0001c0002t0001g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-36-12576A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42227917 | ||||||
| chr22:42228304
|
G | C | 1 | a0001c0002t0002g0138 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-36-12963C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228304 | ||||||
| chr22:42228439
|
A | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-36-13098T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228439 | ||||||
| chr22:42228659
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-36-13318G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228659 | ||||||
| chr22:42228686
|
A | C | 5 | a0002c0003t0001g0058a0002c0003t0001g0060a0002c0003t0001g0062others(2): Show | 5 | NA18949.hp2 NA18960.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-13345T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228686 | ||||||
| chr22:42228729
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36-13388C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228729 | ||||||
| chr22:42228744
|
A | T | 1 | a0001c0002t0001g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-36-13403T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228744 | ||||||
| chr22:42228885
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-36-13544G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228885 | ||||||
| chr22:42228974
|
C | T | 1 | a0002c0003t0001g0040 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-36-13633G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42228974 | ||||||
| chr22:42229230
|
G | C | 2 | a0003c0004t0001g0109a0003c0004t0001g0110 | 2 | HG01243.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-36-13889C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42229230 | ||||||
| chr22:42229503
|
C | G | 75 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(72): Show | 75 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-36-14162G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42229503 | ||||||
| chr22:42229505
|
A | AT | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-14165dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42229505 | ||||||
| chr22:42229634
|
C | G | 1 | a0002c0003t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-36-14293G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42229634 | ||||||
| chr22:42229677
|
C | T | 1 | a0001c0022t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-36-14336G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42229677 | ||||||
| chr22:42230116
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-36-14775C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42230116 | ||||||
| chr22:42230121
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-36-14780T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42230121 | ||||||
| chr22:42230238
|
G | A | 2 | a0001c0002t0002g0138a0008c0024t0001g0037 | 2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-36-14897C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42230238 | ||||||
| chr22:42230454
|
T | C | 2 | a0001c0002t0001g0257a0002c0003t0001g0061 | 2 | HG02015.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-36-15113A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42230454 | ||||||
| chr22:42230642
|
C | CA | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-36-15302dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42230642 | ||||||
| chr22:42230805
|
GTGTT | G | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-15468_-36-1546 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42230805 | ||||||
| chr22:42230901
|
G | A | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-15560C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42230901 | ||||||
| chr22:42231017
|
C | A | 2 | a0001c0002t0001g0306a0001c0002t0001g0330 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-36-15676G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231017 | ||||||
| chr22:42231077
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0170 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-36-15736C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231077 | ||||||
| chr22:42231116
|
T | C | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(238): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.-36-15775A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231116 | ||||||
| chr22:42231117
|
G | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-36-15776C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231117 | ||||||
| chr22:42231284
|
A | G | 4 | a0001c0002t0001g0307a0001c0002t0001g0308a0001c0002t0001g0313others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-15943T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231284 | ||||||
| chr22:42231569
|
T | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-16228A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231569 | ||||||
| chr22:42231858
|
G | A | 1 | a0002c0003t0001g0054 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-36-16517C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231858 | ||||||
| chr22:42231908
|
G | A | 1 | a0001c0002t0001g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-36-16567C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231908 | ||||||
| chr22:42231910
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-36-16569G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231910 | ||||||
| chr22:42231928
|
C | CAAAAA | 60 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0022others(57): Show | 60 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.-36-16592_-36-1658 others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231928 | ||||||
| chr22:42231928
|
C | CAAAAAA | 18 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(15): Show | 18 | HG00438.hp2 HG00735.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-36-16593_-36-1658 others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231928 | ||||||
| chr22:42231928
|
CA | C | 123 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-36-16588delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231928 | ||||||
| chr22:42231928
|
CAA | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-36-16589_-36-1658 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42231928 | ||||||
| chr22:42232057
|
C | T | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-16716G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232057 | ||||||
| chr22:42232069
|
C | T | 3 | a0001c0001t0003g0012a0001c0001t0003g0015a0001c0001t0003g0016 | 3 | HG01891.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-36-16728G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232069 | ||||||
| chr22:42232082
|
T | C | 74 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(71): Show | 74 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-36-16741A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232082 | ||||||
| chr22:42232112
|
C | T | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-16771G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232112 | ||||||
| chr22:42232234
|
T | C | 2 | a0001c0001t0001g0245a0001c0001t0001g0251 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-36-16893A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232234 | ||||||
| chr22:42232252
|
C | T | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-36-16911G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232252 | ||||||
| chr22:42232280
|
G | C | 5 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0145others(2): Show | 5 | NA18940.hp1 NA18967.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-16939C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232280 | ||||||
| chr22:42232329
|
A | G | 29 | a0001c0002t0001g0348a0002c0003t0001g0018a0002c0003t0001g0022others(26): Show | 29 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-36-16988T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232329 | ||||||
| chr22:42232402
|
C | CA | 10 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-36-17062dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232402 | ||||||
| chr22:42232593
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-36-17252G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232593 | ||||||
| chr22:42232689
|
G | A | 1 | a0001c0002t0001g0278 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-36-17348C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232689 | ||||||
| chr22:42232723
|
C | T | 40 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(37): Show | 40 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-36-17382G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232723 | ||||||
| chr22:42232795
|
T | C | 1 | a0009c0025t0001g0019 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-36-17454A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232795 | ||||||
| chr22:42232805
|
G | GA | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.-36-17465dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232805 | ||||||
| chr22:42232805
|
GA | G | 83 | a0001c0001t0002g0014a0001c0001t0002g0096a0001c0001t0003g0011others(80): Show | 83 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-36-17465delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232805 | ||||||
| chr22:42232996
|
G | A | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-17655C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42232996 | ||||||
| chr22:42233079
|
C | T | 1 | a0001c0002t0001g0319 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-36-17738G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42233079 | ||||||
| chr22:42233173
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-36-17832G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42233173 | ||||||
| chr22:42233292
|
G | C | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-36-17951C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42233292 | ||||||
| chr22:42233348
|
A | G | 354 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.-36-18007T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42233348 | ||||||
| chr22:42233363
|
G | A | 6 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-18022C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42233363 | ||||||
| chr22:42233402
|
G | C | 1 | a0004c0005t0002g0239 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-36-18061C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42233402 | ||||||
| chr22:42233923
|
A | T | 1 | a0001c0001t0015g0337 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-36-18582T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42233923 | ||||||
| chr22:42234014
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-36-18673A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42234014 | ||||||
| chr22:42234155
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-18814G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42234155 | ||||||
| chr22:42234336
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-36-18995A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42234336 | ||||||
| chr22:42234739
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-36-19398A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42234739 | ||||||
| chr22:42234748
|
C | G | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-36-19407G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42234748 | ||||||
| chr22:42234766
|
C | T | 4 | a0001c0002t0001g0307a0001c0002t0001g0308a0001c0002t0001g0313others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-19425G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42234766 | ||||||
| chr22:42235041
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-36-19700G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235041 | ||||||
| chr22:42235141
|
C | CA | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.-36-19801dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235141 | ||||||
| chr22:42235141
|
C | CAAA | 6 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(3): Show | 6 | HG02257.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-19803_-36-1980 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235141 | ||||||
| chr22:42235158
|
AG | A | 17 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0267others(14): Show | 17 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-19818delC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235158 | ||||||
| chr22:42235410
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-36-20069G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235410 | ||||||
| chr22:42235433
|
A | G | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-36-20092T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235433 | ||||||
| chr22:42235642
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-36-20301C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235642 | ||||||
| chr22:42235648
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-36-20307C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235648 | ||||||
| chr22:42235767
|
C | T | 4 | a0001c0002t0001g0307a0001c0002t0001g0308a0001c0002t0001g0313others(1): Show | 4 | HG01106.hp1 HG01516.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-20426G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235767 | ||||||
| chr22:42235932
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-20591C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42235932 | ||||||
| chr22:42236096
|
C | T | 1 | a0001c0001t0013g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-36-20755G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236096 | ||||||
| chr22:42236097
|
A | G | 1 | a0002c0003t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-36-20756T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236097 | ||||||
| chr22:42236247
|
TCAAA | T | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-20910_-36-2090 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236247 | ||||||
| chr22:42236280
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-36-20939A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236280 | ||||||
| chr22:42236550
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0016g0147 | 3 | HG01192.hp2 HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-36-21209A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236550 | ||||||
| chr22:42236647
|
G | A | 34 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0001g0267others(31): Show | 34 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.-36-21306C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236647 | ||||||
| chr22:42236741
|
T | G | 3 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0351 | 3 | HG01099.hp1 HG01261.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-36-21400A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236741 | ||||||
| chr22:42236760
|
C | T | 1 | a0001c0010t0006g0008 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-36-21419G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236760 | ||||||
| chr22:42236799
|
C | G | 2 | a0003c0004t0001g0118a0003c0004t0001g0123 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-36-21458G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236799 | ||||||
| chr22:42236826
|
C | T | 36 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0001g0263others(33): Show | 36 | HG01109.hp1 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.-36-21485G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236826 | ||||||
| chr22:42236827
|
G | A | 106 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(103): Show | 106 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-36-21486C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236827 | ||||||
| chr22:42236977
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-36-21636G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42236977 | ||||||
| chr22:42237048
|
T | C | 99 | a0001c0002t0001g0348a0001c0002t0002g0138a0002c0003t0001g0010others(96): Show | 99 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-36-21707A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42237048 | ||||||
| chr22:42237088
|
T | TCTTCCTT others(265): Show |
6 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-21748_-36-2174 others(276): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42237088 | ||||||
| chr22:42237088
|
T | TCTTCCTT others(267): Show |
1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-36-21748_-36-2174 others(278): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42237088 | ||||||
| chr22:42237198
|
G | A | 73 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-21857C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42237198 | ||||||
| chr22:42237383
|
C | A | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-22042G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42237383 | ||||||
| chr22:42237700
|
G | C | 3 | a0001c0001t0004g0095a0007c0011t0004g0244a0007c0011t0004g0254 | 3 | HG02486.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-22359C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42237700 | ||||||
| chr22:42237709
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-36-22368A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42237709 | ||||||
| chr22:42238160
|
A | G | 1 | a0001c0002t0001g0301 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-36-22819T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238160 | ||||||
| chr22:42238200
|
T | A | 1 | a0003c0004t0003g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-36-22859A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238200 | ||||||
| chr22:42238273
|
G | A | 1 | a0003c0004t0003g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-36-22932C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238273 | ||||||
| chr22:42238448
|
G | T | 1 | a0001c0002t0001g0322 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-36-23107C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238448 | ||||||
| chr22:42238532
|
A | G | 16 | a0001c0001t0001g0267a0001c0001t0002g0344a0001c0012t0002g0231others(13): Show | 16 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-36-23191T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238532 | ||||||
| chr22:42238670
|
T | C | 1 | a0002c0003t0001g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-36-23329A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238670 | ||||||
| chr22:42238778
|
C | T | 1 | a0001c0002t0001g0324 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-36-23437G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238778 | ||||||
| chr22:42238828
|
T | C | 1 | a0002c0003t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-36-23487A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238828 | ||||||
| chr22:42238839
|
C | T | 1 | a0004c0005t0002g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-36-23498G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238839 | ||||||
| chr22:42238843
|
C | G | 1 | a0003c0026t0001g0345 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-36-23502G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238843 | ||||||
| chr22:42238855
|
C | T | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-23514G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238855 | ||||||
| chr22:42238934
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-36-23593C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238934 | ||||||
| chr22:42238944
|
T | C | 73 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-23603A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238944 | ||||||
| chr22:42238958
|
AT | A | 73 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-23618delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238958 | ||||||
| chr22:42238962
|
A | AG | 73 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-23622_-36-2362 others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238962 | ||||||
| chr22:42238974
|
C | T | 73 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-23633G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238974 | ||||||
| chr22:42238975
|
A | G | 82 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-36-23634T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238975 | ||||||
| chr22:42238978
|
T | C | 73 | a0001c0002t0001g0348a0002c0003t0001g0010a0002c0003t0001g0018others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-23637A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238978 | ||||||
| chr22:42238982
|
A | G | 82 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-36-23641T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42238982 | ||||||
| chr22:42239035
|
G | A | 1 | a0003c0004t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-36-23694C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239035 | ||||||
| chr22:42239176
|
AACAATTT others(6745): Show |
A | 1 | a0001c0002t0001g0097 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-37+24411_-36-2383 others(4): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239176 | ||||||
| chr22:42239248
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0301 | 2 | HG02027.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-36-23907C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239248 | ||||||
| chr22:42239260
|
T | C | 13 | a0004c0005t0002g0229a0004c0005t0002g0230a0004c0005t0002g0232others(10): Show | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36-23919A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239260 | ||||||
| chr22:42239320
|
T | C | 17 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(14): Show | 17 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.-36-23979A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239320 | ||||||
| chr22:42239333
|
G | A | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-36-23992C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239333 | ||||||
| chr22:42239478
|
G | GA | 350 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-36-24138dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239478 | ||||||
| chr22:42239585
|
C | A | 1 | a0002c0003t0001g0025 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-36-24244G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239585 | ||||||
| chr22:42239589
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36-24248T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239589 | ||||||
| chr22:42239626
|
A | G | 1 | a0001c0028t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-36-24285T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239626 | ||||||
| chr22:42239686
|
G | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-24345C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239686 | ||||||
| chr22:42239870
|
T | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-24529A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42239870 | ||||||
| chr22:42240337
|
C | T | 3 | a0001c0006t0002g0246a0001c0006t0002g0247a0001c0006t0002g0250 | 3 | HG01884.hp2 HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-36-24996G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240337 | ||||||
| chr22:42240601
|
G | T | 6 | a0001c0001t0001g0175a0001c0001t0001g0195a0001c0001t0001g0221others(3): Show | 6 | HG00673.hp2 NA18975.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-25260C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240601 | ||||||
| chr22:42240681
|
T | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-36-25340A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240681 | ||||||
| chr22:42240730
|
C | T | 1 | a0002c0003t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-36-25389G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240730 | ||||||
| chr22:42240805
|
T | C | 5 | a0001c0002t0001g0255a0001c0002t0001g0282a0001c0002t0001g0292others(2): Show | 5 | HG00558.hp1 HG02027.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-25464A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240805 | ||||||
| chr22:42240898
|
C | T | 1 | a0003c0004t0003g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-36-25557G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240898 | ||||||
| chr22:42240943
|
C | G | 1 | a0001c0002t0001g0301 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-36-25602G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240943 | ||||||
| chr22:42240949
|
G | A | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-25608C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240949 | ||||||
| chr22:42240959
|
G | A | 1 | a0002c0003t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-36-25618C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42240959 | ||||||
| chr22:42241017
|
G | A | 16 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(13): Show | 16 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-36-25676C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241017 | ||||||
| chr22:42241076
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0170 | 2 | HG03669.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-36-25735C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241076 | ||||||
| chr22:42241191
|
G | C | 2 | a0001c0002t0007g0102a0001c0002t0007g0103 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-36-25850C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241191 | ||||||
| chr22:42241237
|
T | C | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-25896A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241237 | ||||||
| chr22:42241407
|
C | T | 1 | a0001c0002t0002g0300 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-36-26066G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241407 | ||||||
| chr22:42241415
|
G | A | 2 | a0001c0002t0001g0339a0011c0020t0001g0340 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-36-26074C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241415 | ||||||
| chr22:42241499
|
T | C | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-36-26158A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241499 | ||||||
| chr22:42241552
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-26211G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241552 | ||||||
| chr22:42241813
|
G | A | 1 | a0001c0002t0001g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-36-26472C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241813 | ||||||
| chr22:42241857
|
G | T | 1 | a0001c0001t0002g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-36-26516C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241857 | ||||||
| chr22:42241910
|
T | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-26569A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42241910 | ||||||
| chr22:42242103
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-36-26762G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242103 | ||||||
| chr22:42242134
|
C | T | 15 | a0001c0001t0001g0178a0003c0004t0001g0104a0003c0004t0001g0105others(12): Show | 15 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.-36-26793G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242134 | ||||||
| chr22:42242165
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-26824G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242165 | ||||||
| chr22:42242199
|
C | T | 95 | a0001c0001t0001g0017a0001c0001t0001g0267a0001c0001t0002g0014others(92): Show | 95 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-36-26858G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242199 | ||||||
| chr22:42242202
|
C | CA | 21 | a0001c0001t0001g0293a0001c0001t0002g0092a0001c0001t0015g0337others(18): Show | 21 | HG01258.hp2 HG01496.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.-36-26862dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(4): Show |
1 | a0001c0006t0002g0249 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36-26872_-36-2686 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0245a0001c0001t0001g0251a0005c0009t0008g0355 | 3 | HG02572.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-36-26877_-36-2686 others(20): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(10): Show |
1 | a0016c0029t0022g0354 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-36-26878_-36-2686 others(21): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(12): Show |
2 | a0001c0010t0006g0009a0005c0009t0008g0353 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-36-26880_-36-2686 others(23): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0002g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-36-26862_-36-2686 others(30): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0002g0093 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-36-26862_-36-2686 others(32): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0002g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-36-26862_-36-2686 others(34): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(26): Show |
1 | a0001c0010t0006g0008 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-36-26862_-36-2686 others(37): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
C | CAAAAAAA others(37): Show |
1 | a0012c0018t0002g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-36-26862_-36-2686 others(48): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
CA | C | 46 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(43): Show | 46 | HG00099.hp2 HG00673.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.-36-26862delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
CAA | C | 18 | a0001c0001t0001g0135a0001c0001t0001g0145a0001c0001t0001g0175others(15): Show | 18 | HG00621.hp1 HG00673.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-36-26863_-36-2686 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242202
|
CAAA | C | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-36-26864_-36-2686 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242202 | ||||||
| chr22:42242218
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-36-26878_-36-2687 others(35): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242218 | ||||||
| chr22:42242218
|
A | AAAAAAAA others(6): Show |
1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-36-26878_-36-2687 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242218 | ||||||
| chr22:42242218
|
A | AAAAAAAA others(5): Show |
3 | a0003c0004t0001g0113a0003c0004t0001g0115a0003c0004t0001g0122 | 3 | HG00733.hp2 HG04184.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-36-26878_-36-2687 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242218 | ||||||
| chr22:42242218
|
A | AAAAAAAA others(4): Show |
15 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0109others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.-36-26878_-36-2687 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242218 | ||||||
| chr22:42242218
|
A | AAAAAAAA others(3): Show |
4 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0110others(1): Show | 4 | HG00639.hp1 HG01243.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-26887_-36-2687 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242218 | ||||||
| chr22:42242218
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-36-26877T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242218 | ||||||
| chr22:42242220
|
A | AAAAAAAA others(4): Show |
1 | a0003c0004t0003g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-36-26880_-36-2687 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242220 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(31): Show |
1 | a0002c0003t0001g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-36-26887_-36-2688 others(42): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(26): Show |
3 | a0002c0003t0001g0025a0002c0003t0001g0031a0002c0003t0001g0032 | 3 | HG00140.hp2 HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(37): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(25): Show |
1 | a0002c0003t0001g0027 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-36-26887_-36-2688 others(36): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(24): Show |
3 | a0002c0003t0001g0018a0002c0003t0001g0022a0002c0003t0001g0052 | 3 | HG00323.hp2 HG01106.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(35): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(22): Show |
2 | a0002c0003t0001g0053a0002c0003t0001g0055 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(33): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(21): Show |
1 | a0002c0003t0001g0036 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-36-26887_-36-2688 others(32): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(20): Show |
3 | a0002c0003t0001g0024a0002c0003t0001g0029a0002c0003t0001g0035 | 3 | HG01071.hp1 HG03834.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(31): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(19): Show |
1 | a0002c0003t0001g0034 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-36-26887_-36-2688 others(30): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(13): Show |
1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-26887_-36-2688 others(24): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-36-26887_-36-2688 others(21): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(6): Show |
4 | a0001c0001t0003g0012a0001c0001t0003g0016a0002c0007t0001g0078others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(5): Show |
4 | a0001c0001t0002g0014a0001c0001t0003g0013a0002c0007t0001g0085others(1): Show | 4 | HG02965.hp1 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0003g0015a0002c0003t0001g0056 | 2 | HG01361.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0017a0001c0001t0003g0011 | 2 | HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | AAAAAAT | 8 | a0004c0005t0002g0233a0004c0005t0002g0234a0004c0005t0002g0235others(5): Show | 8 | HG02280.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36-26887_-36-2688 others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242227
|
A | T | 45 | a0001c0012t0002g0231a0002c0003t0001g0010a0002c0003t0001g0020others(42): Show | 45 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-36-26886T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242227 | ||||||
| chr22:42242228
|
C | A | 6 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(3): Show | 6 | HG01433.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-36-26887G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242228 | ||||||
| chr22:42242295
|
G | GAAT | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-26957_-36-2695 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242295 | ||||||
| chr22:42242465
|
A | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-27124T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242465 | ||||||
| chr22:42242486
|
A | G | 4 | a0002c0007t0001g0078a0002c0007t0001g0085a0002c0007t0001g0086others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-27145T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242486 | ||||||
| chr22:42242540
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-36-27199G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242540 | ||||||
| chr22:42242618
|
G | T | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36-27277C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242618 | ||||||
| chr22:42242662
|
G | A | 1 | a0006c0008t0001g0071 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-36-27321C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242662 | ||||||
| chr22:42242674
|
G | A | 2 | a0002c0003t0001g0023a0002c0003t0001g0026 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-36-27333C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42242674 | ||||||
| chr22:42243051
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-37+27288C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243051 | ||||||
| chr22:42243078
|
T | C | 2 | a0001c0001t0002g0096a0001c0001t0002g0344 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-37+27261A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243078 | ||||||
| chr22:42243221
|
A | G | 241 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(238): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.-37+27118T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243221 | ||||||
| chr22:42243253
|
T | C | 1 | a0001c0002t0001g0310 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-37+27086A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243253 | ||||||
| chr22:42243292
|
C | CA | 27 | a0001c0001t0001g0100a0001c0001t0004g0276a0001c0002t0001g0255others(24): Show | 27 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.-37+27046dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAA | 40 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0137others(37): Show | 40 | HG00544.hp2 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-37+27043_-37+2704 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAA | 30 | a0001c0001t0001g0135a0001c0001t0001g0142a0001c0001t0001g0143others(27): Show | 30 | HG00099.hp1 HG00558.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-37+27042_-37+2704 others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAA | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(25): Show | 28 | HG00140.hp1 HG00738.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-37+27041_-37+2704 others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA | 6 | a0001c0001t0001g0141a0001c0001t0001g0153a0001c0001t0001g0168others(3): Show | 6 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+27040_-37+2704 others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0192others(9): Show | 12 | HG02523.hp2 HG02965.hp1 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37+27039_-37+2704 others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(2): Show |
20 | a0001c0001t0001g0201a0002c0003t0001g0031a0002c0003t0001g0032others(17): Show | 20 | HG00140.hp2 HG00673.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37+27038_-37+2704 others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(3): Show |
15 | a0002c0003t0001g0021a0002c0003t0001g0039a0002c0003t0001g0042others(12): Show | 15 | HG00438.hp2 HG00544.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.-37+27037_-37+2704 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0004g0095a0002c0003t0001g0020a0002c0003t0001g0034others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+27036_-37+2704 others(15): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(6): Show |
1 | a0002c0003t0001g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-37+27034_-37+2704 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(7): Show |
1 | a0002c0003t0001g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-37+27033_-37+2704 others(18): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(8): Show |
1 | a0002c0003t0017g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37+27032_-37+2704 others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(9): Show |
2 | a0002c0003t0001g0047a0006c0008t0001g0028 | 2 | NA19068.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-37+27031_-37+2704 others(20): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(11): Show |
1 | a0002c0003t0001g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-37+27029_-37+2704 others(22): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(26): Show |
2 | a0002c0007t0001g0078a0002c0007t0001g0086 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-37+27046_-37+2704 others(37): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(32): Show |
1 | a0002c0007t0003g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-37+27046_-37+2704 others(43): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-37+27046_-37+2704 others(23): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
C | CAAAAAAA others(13): Show |
1 | a0001c0012t0002g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-37+27046_-37+2704 others(24): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
CA | C | 18 | a0001c0001t0001g0101a0001c0001t0001g0263a0001c0001t0001g0264others(15): Show | 18 | HG00738.hp1 HG01074.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37+27046delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
CAAA | C | 10 | a0001c0001t0001g0251a0001c0001t0002g0248a0001c0001t0002g0350others(7): Show | 10 | HG01433.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37+27044_-37+2704 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
CAAAA | C | 7 | a0001c0001t0001g0245a0001c0001t0002g0091a0001c0001t0002g0092others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+27043_-37+2704 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
CAAAAAAA others(2): Show |
C | 12 | a0003c0004t0001g0104a0003c0004t0001g0106a0003c0004t0001g0113others(9): Show | 12 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37+27038_-37+2704 others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
CAAAAAAA others(3): Show |
C | 14 | a0001c0001t0001g0116a0001c0001t0013g0114a0003c0004t0001g0105others(11): Show | 14 | HG00639.hp1 HG01099.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.-37+27037_-37+2704 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243292
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0003t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-37+27032_-37+2704 others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243292 | ||||||
| chr22:42243310
|
A | AAAAAAAA others(19): Show |
1 | a0004c0005t0002g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-37+27028_-37+2702 others(30): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243310 | ||||||
| chr22:42243310
|
A | AAAAAAAA others(16): Show |
2 | a0004c0005t0002g0236a0004c0005t0002g0240 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-37+27028_-37+2702 others(27): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243310 | ||||||
| chr22:42243310
|
A | AAAAAAAA others(15): Show |
3 | a0004c0005t0002g0234a0004c0005t0002g0235a0004c0005t0002g0241 | 3 | HG02280.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-37+27028_-37+2702 others(26): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243310 | ||||||
| chr22:42243310
|
A | AAAAAAAA others(14): Show |
5 | a0004c0005t0002g0230a0004c0005t0002g0232a0004c0005t0002g0233others(2): Show | 5 | HG02647.hp2 HG02976.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+27028_-37+2702 others(25): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243310 | ||||||
| chr22:42243310
|
A | AAAAAAAA others(18): Show |
1 | a0004c0005t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-37+27028_-37+2702 others(29): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243310 | ||||||
| chr22:42243310
|
A | AAAAAAAA others(16): Show |
1 | a0004c0005t0002g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-37+27028_-37+2702 others(27): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243310 | ||||||
| chr22:42243310
|
A | C | 2 | a0001c0001t0001g0267a0001c0012t0002g0231 | 2 | HG02258.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-37+27029T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243310 | ||||||
| chr22:42243326
|
G | C | 3 | a0002c0003t0001g0018a0002c0003t0001g0031a0002c0003t0001g0032 | 3 | HG00140.hp2 HG03490.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-37+27013C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243326 | ||||||
| chr22:42243355
|
C | A | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+26984G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243355 | ||||||
| chr22:42243420
|
C | T | 1 | a0001c0012t0002g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-37+26919G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243420 | ||||||
| chr22:42243539
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-37+26800A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243539 | ||||||
| chr22:42243593
|
C | G | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+26746G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243593 | ||||||
| chr22:42243634
|
G | A | 2 | a0001c0002t0001g0307a0001c0002t0001g0308 | 2 | HG02257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-37+26705C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243634 | ||||||
| chr22:42243639
|
T | G | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-37+26700A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243639 | ||||||
| chr22:42243676
|
G | T | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+26663C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243676 | ||||||
| chr22:42243743
|
G | T | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+26596C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42243743 | ||||||
| chr22:42244123
|
G | A | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+26216C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244123 | ||||||
| chr22:42244276
|
T | C | 2 | a0001c0001t0002g0096a0001c0001t0002g0344 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-37+26063A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244276 | ||||||
| chr22:42244366
|
A | G | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+25973T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244366 | ||||||
| chr22:42244425
|
T | C | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+25914A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244425 | ||||||
| chr22:42244512
|
G | A | 2 | a0003c0004t0001g0104a0003c0004t0001g0105 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-37+25827C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244512 | ||||||
| chr22:42244600
|
G | C | 138 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-37+25739C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244600 | ||||||
| chr22:42244788
|
A | T | 1 | a0001c0002t0001g0327 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-37+25551T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244788 | ||||||
| chr22:42244916
|
C | CA | 13 | a0004c0005t0002g0229a0004c0005t0002g0230a0004c0005t0002g0232others(10): Show | 13 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37+25422dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244916 | ||||||
| chr22:42244916
|
CA | C | 79 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(76): Show | 79 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-37+25422delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244916 | ||||||
| chr22:42244957
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-37+25382G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42244957 | ||||||
| chr22:42245058
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-37+25281C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42245058 | ||||||
| chr22:42245452
|
T | C | 254 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(251): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.-37+24887A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42245452 | ||||||
| chr22:42245529
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-37+24810A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42245529 | ||||||
| chr22:42245664
|
C | A | 1 | a0003c0004t0001g0111 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-37+24675G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42245664 | ||||||
| chr22:42245760
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-37+24579C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42245760 | ||||||
| chr22:42245828
|
G | A | 1 | a0001c0002t0001g0316 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-37+24511C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42245828 | ||||||
| chr22:42245977
|
T | C | 1 | a0003c0026t0001g0345 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-37+24362A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42245977 | ||||||
| chr22:42246041
|
G | A | 3 | a0003c0004t0001g0119a0003c0004t0001g0120a0003c0004t0001g0127 | 3 | HG01070.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-37+24298C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246041 | ||||||
| chr22:42246570
|
T | C | 72 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+23769A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246570 | ||||||
| chr22:42246573
|
C | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+23766G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246573 | ||||||
| chr22:42246696
|
G | A | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+23643C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246696 | ||||||
| chr22:42246837
|
G | A | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+23502C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246837 | ||||||
| chr22:42246873
|
G | C | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-37+23466C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246873 | ||||||
| chr22:42246892
|
G | A | 1 | a0001c0002t0020g0286 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-37+23447C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246892 | ||||||
| chr22:42246899
|
G | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0195a0001c0001t0001g0221others(2): Show | 5 | HG00673.hp2 NA18975.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+23440C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246899 | ||||||
| chr22:42246957
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+23382G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246957 | ||||||
| chr22:42246973
|
T | TA | 9 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(6): Show | 9 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+23365dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42246973 | ||||||
| chr22:42247033
|
A | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-37+23306T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247033 | ||||||
| chr22:42247168
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+23171C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247168 | ||||||
| chr22:42247311
|
G | A | 2 | a0001c0002t0001g0265a0001c0002t0001g0266 | 2 | HG01099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-37+23028C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247311 | ||||||
| chr22:42247439
|
C | CA | 115 | a0001c0001t0001g0017a0001c0001t0001g0116a0001c0001t0001g0154others(112): Show | 115 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37+22899dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247439 | ||||||
| chr22:42247439
|
C | CAA | 16 | a0001c0002t0001g0277a0002c0003t0001g0040a0002c0003t0001g0041others(13): Show | 16 | HG01167.hp2 HG02015.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37+22898_-37+2289 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247439 | ||||||
| chr22:42247526
|
G | A | 4 | a0002c0007t0001g0078a0002c0007t0001g0085a0002c0007t0001g0086others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+22813C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247526 | ||||||
| chr22:42247556
|
C | T | 2 | a0001c0016t0001g0311a0013c0015t0001g0312 | 2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-37+22783G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247556 | ||||||
| chr22:42247777
|
T | TGCTCATT others(6): Show |
7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+22549_-37+2256 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247777 | ||||||
| chr22:42247878
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+22461G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247878 | ||||||
| chr22:42247955
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-37+22384T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42247955 | ||||||
| chr22:42248158
|
G | A | 1 | a0005c0009t0008g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37+22181C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42248158 | ||||||
| chr22:42248465
|
C | T | 17 | a0002c0003t0001g0018a0002c0003t0001g0022a0002c0003t0001g0023others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37+21874G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42248465 | ||||||
| chr22:42248762
|
T | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+21577A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42248762 | ||||||
| chr22:42248915
|
G | A | 3 | a0004c0005t0002g0232a0004c0005t0002g0235a0004c0005t0002g0236 | 3 | HG02280.hp2 HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-37+21424C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42248915 | ||||||
| chr22:42248964
|
G | T | 1 | a0001c0012t0002g0231 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-37+21375C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42248964 | ||||||
| chr22:42249085
|
A | G | 79 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(76): Show | 79 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-37+21254T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249085 | ||||||
| chr22:42249145
|
C | A | 1 | a0002c0003t0001g0061 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-37+21194G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249145 | ||||||
| chr22:42249188
|
C | T | 1 | a0015c0013t0001g0059 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-37+21151G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249188 | ||||||
| chr22:42249196
|
C | T | 72 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+21143G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249196 | ||||||
| chr22:42249232
|
C | T | 1 | a0001c0002t0020g0286 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-37+21107G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249232 | ||||||
| chr22:42249474
|
A | C | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+20865T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249474 | ||||||
| chr22:42249519
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+20820G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249519 | ||||||
| chr22:42249854
|
A | G | 1 | a0001c0002t0014g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-37+20485T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249854 | ||||||
| chr22:42249957
|
T | C | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+20382A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42249957 | ||||||
| chr22:42250090
|
T | C | 3 | a0002c0003t0001g0061a0002c0003t0001g0067a0009c0025t0001g0019 | 3 | NA18947.hp2 NA18977.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.-37+20249A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250090 | ||||||
| chr22:42250168
|
G | A | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+20171C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250168 | ||||||
| chr22:42250209
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+20130G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250209 | ||||||
| chr22:42250267
|
T | G | 4 | a0001c0002t0001g0256a0001c0002t0001g0260a0001c0002t0001g0309others(1): Show | 4 | HG00099.hp2 HG01943.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+20072A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250267 | ||||||
| chr22:42250300
|
C | T | 2 | a0001c0002t0001g0278a0001c0002t0001g0283 | 2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-37+20039G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250300 | ||||||
| chr22:42250446
|
C | CA | 7 | a0001c0001t0004g0095a0001c0002t0001g0313a0001c0002t0007g0103others(4): Show | 7 | HG01106.hp1 HG01243.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+19892dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250446 | ||||||
| chr22:42250446
|
CA | C | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-37+19892delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250446 | ||||||
| chr22:42250446
|
CAA | C | 16 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(13): Show | 16 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-37+19891_-37+1989 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250446 | ||||||
| chr22:42250466
|
AAAG | A | 6 | a0002c0003t0001g0034a0002c0003t0001g0051a0002c0003t0001g0061others(3): Show | 6 | HG01069.hp2 NA18941.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+19870_-37+1987 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250466 | ||||||
| chr22:42250467
|
AAG | A | 64 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(61): Show | 64 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-37+19870_-37+1987 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250467 | ||||||
| chr22:42250476
|
C | T | 2 | a0001c0002t0001g0284a0001c0002t0001g0285 | 2 | NA18939.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.-37+19863G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250476 | ||||||
| chr22:42250508
|
T | C | 1 | a0004c0005t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-37+19831A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250508 | ||||||
| chr22:42250547
|
G | A | 1 | a0002c0003t0017g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37+19792C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250547 | ||||||
| chr22:42250625
|
C | G | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+19714G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250625 | ||||||
| chr22:42250646
|
T | C | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+19693A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250646 | ||||||
| chr22:42250750
|
T | C | 1 | a0003c0004t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-37+19589A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250750 | ||||||
| chr22:42250758
|
A | G | 5 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(2): Show | 5 | NA18947.hp1 NA18964.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+19581T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250758 | ||||||
| chr22:42250965
|
G | C | 5 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(2): Show | 5 | NA18947.hp1 NA18964.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+19374C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42250965 | ||||||
| chr22:42251142
|
G | T | 1 | a0001c0002t0001g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-37+19197C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251142 | ||||||
| chr22:42251332
|
C | T | 1 | a0002c0003t0001g0073 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-37+19007G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251332 | ||||||
| chr22:42251365
|
A | G | 1 | a0001c0002t0002g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-37+18974T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251365 | ||||||
| chr22:42251492
|
C | CT | 58 | a0001c0001t0001g0006a0001c0001t0001g0116a0001c0001t0001g0145others(55): Show | 58 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-37+18846dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251492 | ||||||
| chr22:42251492
|
C | CTT | 47 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0135others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.-37+18845_-37+1884 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251492 | ||||||
| chr22:42251492
|
C | CTTT | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0130others(53): Show | 56 | HG00558.hp2 HG01081.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.-37+18844_-37+1884 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251492 | ||||||
| chr22:42251492
|
C | CTTTT | 20 | a0001c0001t0001g0136a0001c0001t0001g0151a0001c0001t0001g0153others(17): Show | 20 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37+18843_-37+1884 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251492 | ||||||
| chr22:42251492
|
CT | C | 8 | a0001c0001t0001g0101a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG00323.hp1 HG00597.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37+18846delA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251492 | ||||||
| chr22:42251492
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0001g0270 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-37+18837_-37+1884 others(14): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251492 | ||||||
| chr22:42251520
|
T | G | 2 | a0002c0003t0001g0025a0002c0003t0001g0042 | 2 | HG01515.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-37+18819A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251520 | ||||||
| chr22:42251520
|
T | TG | 23 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-37+18818dupC | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251520 | ||||||
| chr22:42251520
|
T | TTG | 37 | a0002c0003t0001g0010a0002c0003t0001g0020a0002c0003t0001g0021others(34): Show | 37 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37+18818_-37+1881 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251520 | ||||||
| chr22:42251520
|
T | TTTG | 14 | a0002c0003t0001g0038a0002c0003t0001g0043a0002c0003t0001g0044others(11): Show | 14 | HG00738.hp1 HG01074.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.-37+18818_-37+1881 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251520 | ||||||
| chr22:42251544
|
C | T | 1 | a0012c0018t0002g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-37+18795G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251544 | ||||||
| chr22:42251692
|
G | A | 1 | a0001c0002t0001g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-37+18647C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251692 | ||||||
| chr22:42251802
|
C | T | 1 | a0003c0004t0001g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-37+18537G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251802 | ||||||
| chr22:42251806
|
A | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+18533T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251806 | ||||||
| chr22:42251868
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+18471C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251868 | ||||||
| chr22:42251920
|
T | C | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+18419A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251920 | ||||||
| chr22:42251980
|
G | T | 1 | a0001c0001t0003g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-37+18359C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42251980 | ||||||
| chr22:42252096
|
T | C | 1 | a0001c0002t0001g0318 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-37+18243A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252096 | ||||||
| chr22:42252111
|
A | AT | 73 | a0001c0002t0001g0336a0002c0003t0001g0010a0002c0003t0001g0018others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37+18227dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252111 | ||||||
| chr22:42252168
|
T | A | 1 | a0006c0008t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-37+18171A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252168 | ||||||
| chr22:42252294
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-37+18045C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252294 | ||||||
| chr22:42252333
|
G | A | 1 | a0004c0005t0002g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-37+18006C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252333 | ||||||
| chr22:42252347
|
T | G | 72 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+17992A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252347 | ||||||
| chr22:42252368
|
C | A | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+17971G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252368 | ||||||
| chr22:42252402
|
C | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-37+17937G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252402 | ||||||
| chr22:42252469
|
T | C | 2 | a0001c0001t0001g0267a0001c0012t0002g0231 | 2 | HG02258.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-37+17870A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252469 | ||||||
| chr22:42252563
|
G | A | 1 | a0002c0003t0001g0065 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-37+17776C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252563 | ||||||
| chr22:42252639
|
C | T | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+17700G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252639 | ||||||
| chr22:42252704
|
G | A | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+17635C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252704 | ||||||
| chr22:42252726
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+17613T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252726 | ||||||
| chr22:42252829
|
A | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-37+17510T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252829 | ||||||
| chr22:42252966
|
A | G | 1 | a0001c0002t0001g0338 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-37+17373T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252966 | ||||||
| chr22:42252967
|
T | C | 1 | a0001c0002t0018g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-37+17372A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42252967 | ||||||
| chr22:42253019
|
G | C | 1 | a0001c0002t0001g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-37+17320C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253019 | ||||||
| chr22:42253292
|
C | T | 2 | a0001c0001t0001g0149a0001c0017t0001g0150 | 2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-37+17047G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253292 | ||||||
| chr22:42253324
|
A | G | 6 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0109others(3): Show | 6 | HG00639.hp1 HG01243.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+17015T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253324 | ||||||
| chr22:42253328
|
G | C | 1 | a0002c0003t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-37+17011C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253328 | ||||||
| chr22:42253376
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0224 | 2 | NA19002.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-37+16963C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253376 | ||||||
| chr22:42253393
|
T | C | 1 | a0001c0002t0001g0341 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37+16946A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253393 | ||||||
| chr22:42253437
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0016g0147 | 3 | HG01192.hp2 HG01516.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-37+16902T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253437 | ||||||
| chr22:42253503
|
C | T | 72 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+16836G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253503 | ||||||
| chr22:42253554
|
G | A | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+16785C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253554 | ||||||
| chr22:42253561
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+16778T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253561 | ||||||
| chr22:42253611
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-37+16728C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42253611 | ||||||
| chr22:42254007
|
C | T | 3 | a0006c0008t0001g0028a0006c0008t0001g0071a0006c0008t0001g0080 | 3 | HG03704.hp1 HG04228.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-37+16332G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254007 | ||||||
| chr22:42254008
|
G | A | 2 | a0001c0002t0007g0102a0001c0002t0007g0103 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-37+16331C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254008 | ||||||
| chr22:42254028
|
A | T | 2 | a0003c0004t0001g0119a0003c0004t0001g0120 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-37+16311T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254028 | ||||||
| chr22:42254044
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-37+16295G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254044 | ||||||
| chr22:42254058
|
A | G | 1 | a0007c0011t0004g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37+16281T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254058 | ||||||
| chr22:42254076
|
C | CA | 33 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0195others(30): Show | 33 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37+16262dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254076 | ||||||
| chr22:42254076
|
C | CAA | 7 | a0001c0001t0001g0017a0001c0001t0002g0094a0001c0001t0004g0095others(4): Show | 7 | HG01081.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+16261_-37+1626 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254076 | ||||||
| chr22:42254076
|
CA | C | 22 | a0001c0001t0001g0116a0001c0001t0001g0142a0001c0001t0001g0143others(19): Show | 22 | HG01433.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.-37+16262delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254076 | ||||||
| chr22:42254317
|
TTTTC | T | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-37+16018_-37+1602 others(8): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254317 | ||||||
| chr22:42254359
|
A | G | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0004g0276others(2): Show | 5 | NA18945.hp2 NA18977.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+15980T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254359 | ||||||
| chr22:42254481
|
T | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+15858A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254481 | ||||||
| chr22:42254657
|
C | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-37+15682G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254657 | ||||||
| chr22:42254672
|
T | C | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+15667A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254672 | ||||||
| chr22:42254774
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-37+15565G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254774 | ||||||
| chr22:42254848
|
C | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0199 | 3 | HG00280.hp2 HG01069.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-37+15491G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254848 | ||||||
| chr22:42254853
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-37+15486A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254853 | ||||||
| chr22:42254914
|
G | A | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+15425C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254914 | ||||||
| chr22:42254959
|
C | CA | 9 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0002t0001g0323others(6): Show | 9 | HG01109.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37+15379dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAA | 102 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-37+15375_-37+1537 others(9): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAA | 55 | a0001c0001t0001g0116a0001c0001t0001g0189a0001c0001t0001g0190others(52): Show | 55 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.-37+15374_-37+1537 others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA | 39 | a0002c0003t0001g0018a0002c0003t0001g0021a0002c0003t0001g0022others(36): Show | 39 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-37+15373_-37+1537 others(11): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(1): Show |
6 | a0002c0003t0001g0048a0002c0003t0001g0049a0002c0003t0001g0050others(3): Show | 6 | HG01109.hp2 HG01361.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+15372_-37+1537 others(12): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0350 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-37+15367_-37+1537 others(17): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0248a0001c0006t0002g0246a0001c0006t0002g0247 | 3 | HG01884.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-37+15366_-37+1537 others(18): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0003g0011a0001c0006t0002g0249a0001c0006t0002g0250others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+15365_-37+1537 others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0251a0001c0001t0003g0012others(2): Show | 5 | HG02257.hp1 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+15364_-37+1537 others(20): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0245a0001c0001t0002g0014a0001c0001t0003g0013 | 3 | HG02895.hp2 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-37+15363_-37+1537 others(21): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(11): Show |
10 | a0001c0001t0002g0091a0001c0001t0003g0015a0001c0010t0006g0008others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37+15362_-37+1537 others(22): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(12): Show |
11 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(8): Show | 11 | HG01891.hp1 HG02109.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37+15361_-37+1537 others(23): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(13): Show |
2 | a0004c0005t0002g0241a0005c0009t0008g0355 | 2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-37+15360_-37+1537 others(24): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-37+15379_-37+1538 others(26): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254959
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-37+15379_-37+1538 others(30): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254959 | ||||||
| chr22:42254979
|
A | G | 1 | a0001c0002t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-37+15360T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42254979 | ||||||
| chr22:42255155
|
C | G | 2 | a0001c0002t0007g0102a0001c0002t0007g0103 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-37+15184G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255155 | ||||||
| chr22:42255215
|
T | C | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-37+15124A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255215 | ||||||
| chr22:42255220
|
C | T | 1 | a0001c0002t0001g0341 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37+15119G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255220 | ||||||
| chr22:42255236
|
C | T | 1 | a0001c0001t0013g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-37+15103G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255236 | ||||||
| chr22:42255367
|
T | G | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+14972A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255367 | ||||||
| chr22:42255413
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-37+14926G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255413 | ||||||
| chr22:42255446
|
G | A | 23 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0091others(20): Show | 23 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-37+14893C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255446 | ||||||
| chr22:42255487
|
C | CAAA | 26 | a0001c0001t0001g0263a0001c0002t0001g0271a0002c0003t0001g0010others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-37+14849_-37+1485 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255487 | ||||||
| chr22:42255488
|
A | AAAAAAC | 30 | a0002c0003t0001g0021a0002c0003t0001g0038a0002c0003t0001g0039others(27): Show | 30 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37+14850_-37+1485 others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255488 | ||||||
| chr22:42255488
|
A | AAAAAACA others(5): Show |
1 | a0002c0003t0001g0082 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-37+14850_-37+1485 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255488 | ||||||
| chr22:42255488
|
A | AAAAAACA others(8): Show |
1 | a0002c0023t0001g0057 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-37+14850_-37+1485 others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255488 | ||||||
| chr22:42255488
|
AAAC | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-37+14848_-37+1485 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255488 | ||||||
| chr22:42255488
|
AAACAAC | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37+14845_-37+1485 others(10): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255488 | ||||||
| chr22:42255488
|
AAACAACA others(2): Show |
A | 7 | a0001c0001t0001g0198a0001c0002t0001g0262a0001c0002t0001g0338others(4): Show | 7 | HG00642.hp1 HG01081.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+14842_-37+1485 others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255488 | ||||||
| chr22:42255488
|
AAACAACA others(5): Show |
A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-37+14839_-37+1485 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255488 | ||||||
| chr22:42255491
|
C | A | 138 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-37+14848G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255491 | ||||||
| chr22:42255494
|
C | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-37+14845G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255494 | ||||||
| chr22:42255497
|
C | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01099.hp1 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37+14842G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255497 | ||||||
| chr22:42255500
|
C | A | 7 | a0001c0001t0001g0198a0001c0002t0001g0262a0001c0002t0001g0338others(4): Show | 7 | HG00642.hp1 HG01081.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+14839G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255500 | ||||||
| chr22:42255503
|
C | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0002t0001g0341 | 3 | HG01496.hp1 HG02293.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37+14836G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255503 | ||||||
| chr22:42255517
|
ACAACAAC others(8): Show |
A | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+14807_-37+1482 others(19): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255517 | ||||||
| chr22:42255520
|
ACAACAAC others(5): Show |
A | 1 | a0016c0029t0022g0354 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37+14807_-37+1481 others(16): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255520 | ||||||
| chr22:42255526
|
A | C | 5 | a0002c0003t0001g0022a0002c0003t0001g0033a0002c0003t0001g0034others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+14813T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255526 | ||||||
| chr22:42255527
|
CAAA | C | 5 | a0002c0003t0001g0022a0002c0003t0001g0033a0002c0003t0001g0034others(2): Show | 5 | HG00323.hp2 HG00735.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+14809_-37+1481 others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255527 | ||||||
| chr22:42255529
|
A | C | 5 | a0002c0003t0001g0018a0002c0003t0001g0029a0002c0003t0001g0030others(2): Show | 5 | HG00140.hp2 HG01433.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37+14810T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255529 | ||||||
| chr22:42255530
|
A | C | 14 | a0002c0003t0001g0018a0002c0003t0001g0023a0002c0003t0001g0024others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37+14809T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255530 | ||||||
| chr22:42255561
|
G | A | 1 | a0001c0002t0001g0342 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-37+14778C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255561 | ||||||
| chr22:42255653
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-37+14686T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255653 | ||||||
| chr22:42255746
|
C | T | 1 | a0001c0001t0012g0205 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-37+14593G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255746 | ||||||
| chr22:42255778
|
TCCTCAGT others(10): Show |
T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-37+14544_-37+1456 others(21): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255778 | ||||||
| chr22:42255961
|
G | A | 250 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.-37+14378C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42255961 | ||||||
| chr22:42256048
|
T | G | 2 | a0007c0011t0004g0244a0007c0011t0004g0254 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-37+14291A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256048 | ||||||
| chr22:42256068
|
G | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-37+14271C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256068 | ||||||
| chr22:42256192
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-37+14147T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256192 | ||||||
| chr22:42256311
|
T | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-37+14028A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256311 | ||||||
| chr22:42256472
|
G | GT | 9 | a0001c0001t0001g0245a0001c0012t0002g0231a0002c0003t0001g0052others(6): Show | 9 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37+13866dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256472 | ||||||
| chr22:42256710
|
T | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.-37+13629A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256710 | ||||||
| chr22:42256846
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-37+13493T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256846 | ||||||
| chr22:42256940
|
C | G | 17 | a0002c0003t0001g0020a0002c0003t0001g0021a0002c0003t0001g0038others(14): Show | 17 | HG02015.hp1 HG02027.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-37+13399G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42256940 | ||||||
| chr22:42257019
|
G | C | 2 | a0001c0010t0006g0008a0001c0010t0006g0009 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-37+13320C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42257019 | ||||||
| chr22:42257032
|
T | C | 248 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-37+13307A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42257032 | ||||||
| chr22:42257046
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-37+13293C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42257046 | ||||||
| chr22:42257671
|
T | C | 6 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG01891.hp1 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+12668A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42257671 | ||||||
| chr22:42257846
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-37+12493C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42257846 | ||||||
| chr22:42257896
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-37+12443G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42257896 | ||||||
| chr22:42258041
|
C | T | 1 | a0001c0028t0001g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-37+12298G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258041 | ||||||
| chr22:42258271
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01496.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-37+12068G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258271 | ||||||
| chr22:42258301
|
CAA | C | 15 | a0001c0001t0001g0267a0001c0012t0002g0231a0004c0005t0002g0229others(12): Show | 15 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+12036_-37+1203 others(6): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258301 | ||||||
| chr22:42258320
|
T | G | 1 | a0001c0021t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-37+12019A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258320 | ||||||
| chr22:42258321
|
C | G | 16 | a0002c0003t0001g0018a0002c0003t0001g0022a0002c0003t0001g0023others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37+12018G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258321 | ||||||
| chr22:42258364
|
C | T | 1 | a0001c0001t0013g0114 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-37+11975G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258364 | ||||||
| chr22:42258414
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+11925T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258414 | ||||||
| chr22:42258910
|
G | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+11429C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42258910 | ||||||
| chr22:42259277
|
G | T | 25 | a0001c0001t0001g0116a0001c0001t0013g0114a0003c0004t0001g0104others(22): Show | 25 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-37+11062C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259277 | ||||||
| chr22:42259342
|
G | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+10997C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259342 | ||||||
| chr22:42259371
|
G | T | 72 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+10968C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259371 | ||||||
| chr22:42259446
|
T | C | 1 | a0004c0005t0002g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-37+10893A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259446 | ||||||
| chr22:42259727
|
C | A | 1 | a0007c0011t0004g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37+10612G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259727 | ||||||
| chr22:42259865
|
G | A | 1 | a0001c0002t0001g0343 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-37+10474C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259865 | ||||||
| chr22:42259924
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0344 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-37+10415C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259924 | ||||||
| chr22:42259939
|
C | T | 9 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+10400G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42259939 | ||||||
| chr22:42260264
|
A | G | 2 | a0001c0001t0004g0095a0007c0011t0004g0244 | 2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-37+10075T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42260264 | ||||||
| chr22:42260452
|
G | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+9887C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42260452 | ||||||
| chr22:42260582
|
A | T | 80 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(77): Show | 80 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.-37+9757T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42260582 | ||||||
| chr22:42260633
|
C | G | 1 | a0004c0005t0002g0230 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-37+9706G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42260633 | ||||||
| chr22:42260675
|
G | A | 24 | a0003c0004t0001g0104a0003c0004t0001g0105a0003c0004t0001g0106others(21): Show | 24 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-37+9664C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42260675 | ||||||
| chr22:42260884
|
T | A | 8 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37+9455A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42260884 | ||||||
| chr22:42261147
|
G | A | 2 | a0002c0003t0001g0081a0002c0003t0001g0082 | 2 | NA19010.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-37+9192C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261147 | ||||||
| chr22:42261241
|
CTGA | C | 9 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0248others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+9095_-37+9097d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261241 | ||||||
| chr22:42261246
|
G | A | 2 | a0002c0003t0001g0083a0003c0026t0001g0345 | 2 | HG00544.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-37+9093C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261246 | ||||||
| chr22:42261389
|
T | C | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+8950A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261389 | ||||||
| chr22:42261471
|
CCTA | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | NA18973.hp2 NA18995.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-37+8865_-37+8867d others(5): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261471 | ||||||
| chr22:42261555
|
A | AT | 6 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+8783dupA | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261555 | ||||||
| chr22:42261560
|
T | G | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-37+8779A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261560 | ||||||
| chr22:42261594
|
C | CA | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG01891.hp2 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37+8744dupT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261594 | ||||||
| chr22:42261595
|
A | G | 1 | a0006c0008t0001g0028 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-37+8744T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261595 | ||||||
| chr22:42261694
|
G | T | 1 | a0001c0002t0002g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-37+8645C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261694 | ||||||
| chr22:42261695
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-37+8644C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261695 | ||||||
| chr22:42261764
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-37+8575A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261764 | ||||||
| chr22:42261803
|
C | T | 6 | a0003c0004t0001g0107a0003c0004t0001g0108a0003c0004t0001g0109others(3): Show | 6 | HG00639.hp1 HG01243.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+8536G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261803 | ||||||
| chr22:42261814
|
G | A | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+8525C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42261814 | ||||||
| chr22:42262066
|
G | A | 2 | a0001c0002t0007g0102a0001c0002t0007g0103 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-37+8273C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42262066 | ||||||
| chr22:42262225
|
A | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02280.hp1 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+8114T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42262225 | ||||||
| chr22:42262381
|
A | G | 2 | a0001c0002t0001g0265a0001c0002t0001g0266 | 2 | HG01099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-37+7958T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42262381 | ||||||
| chr22:42262754
|
G | A | 3 | a0002c0007t0001g0085a0002c0007t0001g0086a0002c0007t0003g0084 | 3 | HG02965.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-37+7585C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42262754 | ||||||
| chr22:42262815
|
C | T | 5 | a0002c0003t0001g0023a0002c0003t0001g0024a0002c0003t0001g0025others(2): Show | 5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+7524G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42262815 | ||||||
| chr22:42262875
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG01109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-37+7464T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42262875 | ||||||
| chr22:42263104
|
G | A | 1 | a0001c0002t0001g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-37+7235C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42263104 | ||||||
| chr22:42263529
|
C | T | 1 | a0003c0004t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37+6810G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42263529 | ||||||
| chr22:42263790
|
C | T | 1 | a0003c0004t0001g0351 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-37+6549G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42263790 | ||||||
| chr22:42263958
|
G | A | 16 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(13): Show | 16 | HG00639.hp2 HG00642.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-37+6381C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42263958 | ||||||
| chr22:42264257
|
A | C | 1 | a0007c0011t0004g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37+6082T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42264257 | ||||||
| chr22:42264408
|
A | G | 81 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(78): Show | 81 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-37+5931T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42264408 | ||||||
| chr22:42264521
|
C | G | 1 | a0016c0029t0022g0354 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37+5818G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42264521 | ||||||
| chr22:42264729
|
C | T | 1 | a0005c0009t0008g0353 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37+5610G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42264729 | ||||||
| chr22:42265138
|
A | G | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-37+5201T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42265138 | ||||||
| chr22:42265201
|
G | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG00673.hp2 NA18945.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+5138C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42265201 | ||||||
| chr22:42265258
|
G | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+5081C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42265258 | ||||||
| chr22:42265665
|
G | A | 8 | a0001c0001t0002g0014a0001c0001t0003g0011a0001c0001t0003g0012others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37+4674C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42265665 | ||||||
| chr22:42265929
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-37+4410T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42265929 | ||||||
| chr22:42266082
|
TA | T | 112 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-37+4256delT | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266082 | ||||||
| chr22:42266092
|
A | T | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | HG02109.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-37+4247T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266092 | ||||||
| chr22:42266341
|
A | C | 1 | a0001c0001t0001g0130 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-37+3998T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266341 | ||||||
| chr22:42266365
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-37+3974G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266365 | ||||||
| chr22:42266495
|
T | C | 72 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+3844A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266495 | ||||||
| chr22:42266512
|
C | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+3827G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266512 | ||||||
| chr22:42266967
|
A | G | 1 | a0001c0002t0001g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-37+3372T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266967 | ||||||
| chr22:42266978
|
CAATTT | C | 15 | a0001c0012t0002g0231a0004c0005t0002g0229a0004c0005t0002g0230others(12): Show | 15 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37+3356_-37+3360d others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42266978 | ||||||
| chr22:42267144
|
G | T | 1 | a0012c0018t0002g0243 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-37+3195C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267144 | ||||||
| chr22:42267204
|
T | C | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+3135A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267204 | ||||||
| chr22:42267236
|
C | T | 14 | a0001c0012t0002g0231a0004c0005t0002g0229a0004c0005t0002g0230others(11): Show | 14 | HG02280.hp2 HG02451.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37+3103G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267236 | ||||||
| chr22:42267297
|
T | C | 1 | a0002c0003t0021g0087 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-37+3042A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267297 | ||||||
| chr22:42267302
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-37+3037A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267302 | ||||||
| chr22:42267403
|
T | A | 1 | a0001c0002t0001g0346 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-37+2936A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267403 | ||||||
| chr22:42267741
|
G | T | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+2598C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267741 | ||||||
| chr22:42267764
|
C | T | 1 | a0001c0002t0001g0256 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-37+2575G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267764 | ||||||
| chr22:42267769
|
A | T | 1 | a0001c0002t0001g0255 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-37+2570T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267769 | ||||||
| chr22:42267834
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-37+2505A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267834 | ||||||
| chr22:42267865
|
C | G | 72 | a0002c0003t0001g0010a0002c0003t0001g0018a0002c0003t0001g0020others(69): Show | 72 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+2474G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267865 | ||||||
| chr22:42267868
|
A | G | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-37+2471T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267868 | ||||||
| chr22:42267916
|
C | A | 1 | a0002c0003t0001g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-37+2423G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267916 | ||||||
| chr22:42267977
|
C | T | 1 | a0002c0003t0001g0021 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-37+2362G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42267977 | ||||||
| chr22:42268100
|
C | T | 1 | a0002c0003t0001g0020 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-37+2239G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268100 | ||||||
| chr22:42268123
|
A | G | 2 | a0001c0010t0006g0008a0001c0010t0006g0009 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-37+2216T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268123 | ||||||
| chr22:42268125
|
A | T | 2 | a0001c0010t0006g0008a0001c0010t0006g0009 | 2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-37+2214T>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268125 | ||||||
| chr22:42268156
|
T | TAAATA | 82 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-37+2178_-37+2182d others(7): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268156 | ||||||
| chr22:42268167
|
G | A | 1 | a0002c0003t0001g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-37+2172C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268167 | ||||||
| chr22:42268195
|
A | C | 105 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-37+2144T>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268195 | ||||||
| chr22:42268237
|
T | C | 5 | a0001c0001t0002g0014a0001c0001t0003g0012a0001c0001t0003g0013others(2): Show | 5 | HG01891.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37+2102A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268237 | ||||||
| chr22:42268366
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-37+1973A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268366 | ||||||
| chr22:42268390
|
G | T | 1 | a0009c0025t0001g0019 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-37+1949C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268390 | ||||||
| chr22:42268492
|
G | T | 1 | a0001c0002t0014g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-37+1847C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268492 | ||||||
| chr22:42268632
|
C | T | 1 | a0002c0003t0001g0018 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-37+1707G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268632 | ||||||
| chr22:42268877
|
T | A | 81 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(78): Show | 81 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-37+1462A>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268877 | ||||||
| chr22:42268938
|
T | C | 1 | a0003c0004t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-37+1401A>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268938 | ||||||
| chr22:42268966
|
T | G | 71 | a0002c0003t0001g0018a0002c0003t0001g0020a0002c0003t0001g0021others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-37+1373A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42268966 | ||||||
| chr22:42269111
|
C | T | 27 | a0001c0001t0001g0116a0001c0001t0013g0114a0003c0004t0001g0104others(24): Show | 27 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-37+1228G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269111 | ||||||
| chr22:42269322
|
G | A | 1 | a0005c0009t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37+1017C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269322 | ||||||
| chr22:42269388
|
C | T | 2 | a0003c0004t0001g0104a0003c0004t0001g0105 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-37+951G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269388 | ||||||
| chr22:42269417
|
A | G | 6 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG02280.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37+922T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269417 | ||||||
| chr22:42269470
|
C | G | 1 | a0001c0002t0001g0097 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-37+869G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269470 | ||||||
| chr22:42269580
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-37+759G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269580 | ||||||
| chr22:42269707
|
TCCTGCGC others(6): Show |
T | 1 | a0001c0001t0004g0095 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-37+619_-37+631del others(13): Show |
TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269707 | ||||||
| chr22:42269762
|
G | A | 1 | a0003c0004t0003g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-37+577C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269762 | ||||||
| chr22:42269854
|
C | T | 7 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(4): Show | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37+485G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269854 | ||||||
| chr22:42269980
|
G | A | 1 | a0001c0002t0001g0348 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-37+359C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42269980 | ||||||
| chr22:42270020
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37+319G>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270020 | ||||||
| chr22:42270025
|
G | A | 1 | a0001c0002t0001g0349 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-37+314C>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270025 | ||||||
| chr22:42270063
|
A | G | 82 | a0001c0001t0001g0017a0001c0001t0002g0014a0001c0001t0003g0011others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-37+276T>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270063 | ||||||
| chr22:42270091
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007 | 3 | NA18973.hp2 NA18995.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-37+248C>A | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270091 | ||||||
| chr22:42270126
|
G | C | 1 | a0001c0001t0002g0350 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-37+213C>G | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270126 | ||||||
| chr22:42270163
|
C | G | 1 | a0001c0001t0001g0004 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-37+176G>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270163 | ||||||
| chr22:42270181
|
C | A | 1 | a0003c0004t0001g0351 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-37+158G>T | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270181 | ||||||
| chr22:42270197
|
T | G | 1 | a0010c0014t0001g0352 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-37+142A>C | TCF20 | ENSG00000100207.21 | transcript | ENST00000677622.1 | protein_coding | 1/5 | chr22 | 42270197 |