Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22980 |
|---|---|
| ensemblid | ENSG00000141002.20 |
| hgncid | 29181 |
| symbol | TCF25 |
| name | transcription factor 25 |
| refseq_nuc | NM_014972.3 |
| refseq_prot | NP_055787.1 |
| ensembl_nuc | ENST00000263346.13 |
| ensembl_prot | ENSP00000263346.8 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 89873592 |
| end | 89911379 |
| strand | + |
| ver | v1.2 |
| region | chr16:89873592-89911379 |
| region5000 | chr16:89868592-89916379 |
| regionname0 | TCF25_chr16_89873592_89911379 |
| regionname5000 | TCF25_chr16_89868592_89916379 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 676 | 269 | 70 | 62 | 84 | 14 | 37 | 51 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0002 | 0/0 | 676 | 24 | 18 | 2 | 0 | 0 | 4 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0003 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0004 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0005 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0006 | 0/0 | 676 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0007 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0008 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0009 | 0/0 | 676 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| 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 | 1/1 | 2031 | 221 | 56 | 60 | 57 | 13 | 33 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0002 | 0/0 | 2031 | 28 | 0 | 1 | 24 | 1 | 2 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0003 | 0/0 | 2031 | 22 | 16 | 2 | 0 | 0 | 4 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0004 | 0/0 | 2031 | 14 | 14 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0005 | 0/0 | 2031 | 5 | 0 | 0 | 3 | 0 | 2 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0006 | 0/0 | 2031 | 2 | 2 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0007 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0008 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0009 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0010 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0011 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0012 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0013 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| c0014 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 218 | 279 | 71 | 64 | 87 | 14 | 41 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| t0002 | 0/0 | 218 | 18 | 18 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| t0003 | 0/0 | 218 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| t0004 | 0/0 | 218 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| t0005 | 0/0 | 218 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| 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 | 1/1 | 2031 | 221 | 56 | 60 | 57 | 13 | 33 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0002 | 0/0 | 2031 | 28 | 0 | 1 | 24 | 1 | 2 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0004 | 0/0 | 2031 | 14 | 14 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0005 | 0/0 | 2031 | 5 | 0 | 0 | 3 | 0 | 2 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0010 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0002c0003 | 0/0 | 2031 | 22 | 16 | 2 | 0 | 0 | 4 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0002c0006 | 0/0 | 2031 | 2 | 2 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0003c0014 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0004c0012 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0005c0007 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0006c0009 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0007c0008 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0008c0011 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0009c0013 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2248 | 220 | 55 | 60 | 57 | 13 | 33 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0001t0003 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0002t0001 | 0/0 | 2248 | 27 | 0 | 1 | 23 | 1 | 2 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0002t0005 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0004t0002 | 0/0 | 2248 | 14 | 14 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0005t0001 | 0/0 | 2248 | 4 | 0 | 0 | 3 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0005t0004 | 0/0 | 2248 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0001c0010t0001 | 0/0 | 2248 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0002c0003t0001 | 0/0 | 2248 | 22 | 16 | 2 | 0 | 0 | 4 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0002c0006t0002 | 0/0 | 2248 | 2 | 2 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0003c0014t0001 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0004c0012t0001 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0005c0007t0001 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0006c0009t0002 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0007c0008t0001 | 0/0 | 2248 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0008c0011t0001 | 0/0 | 2248 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| a0009c0013t0002 | 0/0 | 2248 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | copy fasta | chr16 | 89868592 | 89916379 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0002t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0004t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0005t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0005t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0005t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0001c0010t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0006t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0002c0006t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0003c0014t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0004c0012t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0005c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0006c0009t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0007c0008t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0008c0011t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| a0009c0013t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0042 | EUR | FIN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | FIN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0288 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00642 | hp1 | a0001 | c0010 | t0001 | g0002 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | CHS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0276 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01891 | hp2 | a0001 | c0004 | t0002 | g0097 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02040 | hp1 | a0005 | c0007 | t0001 | g0047 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02055 | hp1 | a0001 | c0004 | t0002 | g0068 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02055 | hp2 | a0006 | c0009 | t0002 | g0072 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02145 | hp1 | a0001 | c0004 | t0002 | g0069 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CDX | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | CDX | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0287 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0067 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0279 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02622 | hp2 | a0001 | c0004 | t0002 | g0263 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0285 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02698 | hp1 | a0007 | c0008 | t0001 | g0056 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02717 | hp1 | a0001 | c0004 | t0002 | g0071 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02717 | hp2 | a0002 | c0006 | t0002 | g0190 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02809 | hp2 | a0002 | c0006 | t0002 | g0182 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0290 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0289 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0286 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0066 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0059 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02976 | hp2 | a0001 | c0004 | t0002 | g0064 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0280 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0281 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03209 | hp2 | a0001 | c0004 | t0002 | g0058 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03669 | hp2 | a0001 | c0005 | t0004 | g0271 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03688 | hp1 | a0002 | c0003 | t0001 | g0277 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03704 | hp1 | a0001 | c0005 | t0001 | g0267 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0283 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0274 | SAS | BEB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0191 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CHB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18940 | hp1 | a0004 | c0012 | t0001 | g0257 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18951 | hp1 | a0001 | c0005 | t0001 | g0268 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18960 | hp1 | a0003 | c0014 | t0001 | g0026 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18979 | hp1 | a0001 | c0005 | t0001 | g0269 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18983 | hp1 | a0008 | c0011 | t0001 | g0120 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0282 | AFR | LWK | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0065 | AFR | LWK | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0275 | AFR | LWK | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19057 | hp2 | a0001 | c0005 | t0001 | g0266 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19074 | hp2 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19240 | hp1 | a0009 | c0013 | t0002 | g0060 | AFR | YRI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0053 | AFR | ASW | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20129 | hp2 | a0001 | c0004 | t0002 | g0063 | AFR | ASW | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0278 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0070 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0052 | AFR | MSL | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | USA | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA20300 | hp2 | a0001 | c0004 | t0002 | g0061 | AFR | USA | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | LWK | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0137 | REF | REF | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | TCF25_chr16_89868592_89916379 | TCF25 | chr16 | 89868592 | 89916379 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89873824
|
A | C | 1 | a0002 | 24 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(21): Show |
missense_variant | MODERATE | c.157A>C | p.Lys53Gln | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/18 | 233/2248 | 157/2031 | 53/676 | chr16 | 89873824 | ||
| chr16:89892260
|
C | T | 1 | a0003 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.682C>T | p.Arg228Cys | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/18 | 758/2248 | 682/2031 | 228/676 | chr16 | 89892260 | ||
| chr16:89898583
|
A | G | 1 | a0009 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1049A>G | p.Gln350Arg | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 10/18 | 1125/2248 | 1049/2031 | 350/676 | chr16 | 89898583 | ||
| chr16:89898585
|
A | T | 1 | a0004 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1051A>T | p.Met351Leu | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 10/18 | 1127/2248 | 1051/2031 | 351/676 | chr16 | 89898585 | ||
| chr16:89900641
|
C | T | 1 | a0008 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.1228C>T | p.Arg410Trp | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/18 | 1304/2248 | 1228/2031 | 410/676 | chr16 | 89900641 | ||
| chr16:89900656
|
C | T | 1 | a0005 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1243C>T | p.Leu415Phe | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/18 | 1319/2248 | 1243/2031 | 415/676 | chr16 | 89900656 | ||
| chr16:89910625
|
C | T | 1 | a0006 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1834C>T | p.Leu612Phe | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 17/18 | 1910/2248 | 1834/2031 | 612/676 | chr16 | 89910625 | ||
| chr16:89911117
|
A | T | 1 | a0007 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1910A>T | p.Asn637Ile | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 18/18 | 1986/2248 | 1910/2031 | 637/676 | chr16 | 89911117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89898647
|
G | A | 3 | a0001c0002a0003c0014a0005c0007 | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
splice_region_variant&synonymous_variant | LOW | c.1113G>A | p.Leu371Leu | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 10/18 | 1189/2248 | 1113/2031 | 371/676 | chr16 | 89898647 | ||
| chr16:89904158
|
C | T | 3 | a0001c0004a0002c0006a0009c0013 | 17 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
synonymous_variant | LOW | c.1422C>T | p.Asp474Asp | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/18 | 1498/2248 | 1422/2031 | 474/676 | chr16 | 89904158 | ||
| chr16:89905061
|
C | T | 1 | a0001c0010 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1593C>T | p.Asp531Asp | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/18 | 1669/2248 | 1593/2031 | 531/676 | chr16 | 89905061 | ||
| chr16:89911196
|
G | A | 1 | a0001c0005 | 5 | HG03669.hp2 HG03704.hp1 NA18951.hp1 others(2): Show |
synonymous_variant | LOW | c.1989G>A | p.Ala663Ala | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 18/18 | 2065/2248 | 1989/2031 | 663/676 | chr16 | 89911196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89873629
|
C | T | 1 | a0001c0002t0005 | 1 | NA19074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/18 | 39 | chr16 | 89873629 | |||||
| chr16:89911245
|
G | A | 1 | a0001c0001t0003 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 18/18 | 7 | chr16 | 89911245 | |||||
| chr16:89911281
|
G | A | 4 | a0001c0004t0002a0002c0006t0002a0006c0009t0002others(1): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 18/18 | 43 | chr16 | 89911281 | |||||
| chr16:89911331
|
G | A | 1 | a0001c0005t0004 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 18/18 | 93 | chr16 | 89911331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:89873883
|
G | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.192+24G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89873883 | ||||||
| chr16:89873935
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192+76C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89873935 | ||||||
| chr16:89873978
|
G | T | 20 | a0001c0001t0001g0291a0001c0001t0003g0292a0002c0003t0001g0005others(17): Show | 21 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+119G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89873978 | ||||||
| chr16:89873986
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+127C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89873986 | ||||||
| chr16:89874128
|
G | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.192+269G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874128 | ||||||
| chr16:89874170
|
G | A | 18 | a0002c0003t0001g0005a0002c0003t0001g0274a0002c0003t0001g0275others(15): Show | 19 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.192+311G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874170 | ||||||
| chr16:89874200
|
A | C | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.192+341A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874200 | ||||||
| chr16:89874265
|
C | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.192+406C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874265 | ||||||
| chr16:89874326
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+467C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874326 | ||||||
| chr16:89874332
|
G | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0022 | 2 | HG02165.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.192+473G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874332 | ||||||
| chr16:89874421
|
C | T | 6 | a0002c0003t0001g0285a0002c0003t0001g0286a0002c0003t0001g0287others(3): Show | 6 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+562C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874421 | ||||||
| chr16:89874507
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.192+648C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874507 | ||||||
| chr16:89874534
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+675C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874534 | ||||||
| chr16:89874569
|
C | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.192+710C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874569 | ||||||
| chr16:89874642
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.192+783A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874642 | ||||||
| chr16:89874667
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.192+808A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874667 | ||||||
| chr16:89874745
|
T | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 47 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.192+886T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874745 | ||||||
| chr16:89874843
|
C | T | 1 | a0001c0004t0002g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.192+984C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874843 | ||||||
| chr16:89874972
|
C | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.192+1113C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89874972 | ||||||
| chr16:89875030
|
T | C | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.192+1171T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875030 | ||||||
| chr16:89875080
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.192+1221A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875080 | ||||||
| chr16:89875082
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0193others(67): Show | 72 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.192+1223C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875082 | ||||||
| chr16:89875154
|
T | C | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.192+1295T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875154 | ||||||
| chr16:89875190
|
A | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.192+1331A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875190 | ||||||
| chr16:89875392
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0193 | 2 | HG03710.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.192+1533G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875392 | ||||||
| chr16:89875427
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.192+1568C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875427 | ||||||
| chr16:89875449
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.192+1590A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875449 | ||||||
| chr16:89875495
|
A | G | 9 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(6): Show | 9 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+1636A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875495 | ||||||
| chr16:89875513
|
G | GT | 38 | a0001c0001t0001g0051a0001c0001t0001g0054a0001c0001t0001g0163others(35): Show | 38 | HG00099.hp2 HG00621.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.192+1681dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875513 | |||||
| chr16:89875513
|
G | GTT | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+1680_192+1681d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875513 | |||||
| chr16:89875513
|
GT | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.192+1681delT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875513 | |||||
| chr16:89875513
|
GTT | G | 46 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 46 | HG00597.hp2 HG00609.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.192+1680_192+1681d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875513 | |||||
| chr16:89875513
|
GTTTTTTT others(4): Show |
G | 1 | a0007c0008t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.192+1671_192+1681d others(13): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875513 | |||||
| chr16:89875513
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.192+1670_192+1681d others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875513 | |||||
| chr16:89875562
|
G | A | 1 | a0002c0003t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.192+1703G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875562 | ||||||
| chr16:89875578
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.192+1719A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875578 | ||||||
| chr16:89875669
|
C | G | 20 | a0002c0003t0001g0005a0002c0003t0001g0274a0002c0003t0001g0275others(17): Show | 21 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+1810C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875669 | ||||||
| chr16:89875702
|
T | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0073others(34): Show | 38 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.192+1843T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875702 | ||||||
| chr16:89875757
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.192+1898C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875757 | ||||||
| chr16:89875758
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.192+1899G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875758 | ||||||
| chr16:89875817
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.192+1958T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875817 | ||||||
| chr16:89875820
|
C | CT | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(125): Show | 129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.192+1989dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
C | CTT | 31 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0085others(28): Show | 31 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+1988_192+1989d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
C | CTTT | 9 | a0001c0001t0001g0020a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 9 | HG01256.hp2 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+1987_192+1989d others(5): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
C | CTTTTTTT others(1): Show |
7 | a0002c0003t0001g0005a0002c0003t0001g0278a0002c0003t0001g0279others(4): Show | 8 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+1982_192+1989d others(10): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
C | CTTTTTTT others(3): Show |
3 | a0001c0005t0001g0267a0001c0005t0001g0268a0002c0003t0001g0191 | 3 | HG03704.hp1 HG04204.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.192+1980_192+1989d others(12): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
C | CTTTTTTT others(4): Show |
1 | a0001c0005t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.192+1979_192+1989d others(13): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0270a0001c0005t0004g0271 | 2 | HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.192+1978_192+1989d others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0055a0001c0001t0001g0110a0001c0004t0002g0097 | 3 | HG01891.hp2 HG02027.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.192+1979_192+1989d others(13): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875820
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+1976_192+1989d others(16): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875820 | |||||
| chr16:89875964
|
C | G | 20 | a0002c0003t0001g0005a0002c0003t0001g0274a0002c0003t0001g0275others(17): Show | 21 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+2105C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875964 | ||||||
| chr16:89875970
|
T | A | 1 | a0001c0001t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.192+2111T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875970 | ||||||
| chr16:89875982
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0169 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.192+2123T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89875982 | ||||||
| chr16:89875989
|
C | CT | 18 | a0001c0001t0001g0062a0001c0001t0001g0098a0001c0004t0002g0058others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+2139dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875989 | |||||
| chr16:89875989
|
CT | C | 9 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(6): Show | 9 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+2139delT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89875989 | |||||
| chr16:89876087
|
G | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.192+2228G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876087 | ||||||
| chr16:89876311
|
T | C | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.192+2452T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876311 | ||||||
| chr16:89876372
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.192+2513C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876372 | ||||||
| chr16:89876373
|
G | A | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.192+2514G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876373 | ||||||
| chr16:89876409
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.192+2550G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876409 | ||||||
| chr16:89876610
|
G | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0074others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.192+2751G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876610 | ||||||
| chr16:89876643
|
TG | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(13): Show | 16 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.192+2787delG | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89876643 | |||||
| chr16:89876723
|
C | G | 25 | a0001c0001t0001g0018a0001c0001t0001g0264a0001c0001t0001g0291others(22): Show | 26 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.192+2864C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876723 | ||||||
| chr16:89876806
|
A | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.192+2947A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876806 | ||||||
| chr16:89876860
|
C | T | 1 | a0007c0008t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.192+3001C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876860 | ||||||
| chr16:89876915
|
C | T | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.192+3056C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876915 | ||||||
| chr16:89876927
|
T | TA | 39 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0075others(36): Show | 39 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.192+3093dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89876927 | |||||
| chr16:89876927
|
T | TAA | 42 | a0001c0001t0001g0264a0001c0001t0003g0292a0001c0002t0001g0021others(39): Show | 43 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+3092_192+3093d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89876927 | |||||
| chr16:89876927
|
T | TAAA | 21 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(18): Show | 21 | HG00621.hp1 HG01109.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+3091_192+3093d others(5): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89876927 | |||||
| chr16:89876988
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192+3129G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89876988 | ||||||
| chr16:89877076
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.192+3217C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877076 | ||||||
| chr16:89877077
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.192+3218G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877077 | ||||||
| chr16:89877101
|
C | CA | 20 | a0001c0001t0001g0062a0001c0001t0001g0098a0001c0004t0002g0058others(17): Show | 20 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.192+3249dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89877101 | |||||
| chr16:89877109
|
T | A | 68 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 69 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.192+3250T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877109 | ||||||
| chr16:89877113
|
T | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 51 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.192+3254T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877113 | ||||||
| chr16:89877115
|
A | AT | 20 | a0002c0003t0001g0005a0002c0003t0001g0052a0002c0003t0001g0053others(17): Show | 21 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+3256_192+3257i others(3): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877115 | ||||||
| chr16:89877115
|
A | T | 4 | a0001c0001t0001g0264a0001c0001t0001g0291a0002c0003t0001g0277others(1): Show | 4 | HG00099.hp2 HG02055.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+3256A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877115 | ||||||
| chr16:89877116
|
A | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+3257A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877116 | ||||||
| chr16:89877117
|
T | A | 31 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(28): Show | 32 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.192+3258T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877117 | ||||||
| chr16:89877175
|
C | G | 1 | a0001c0002t0001g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.192+3316C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877175 | ||||||
| chr16:89877221
|
G | A | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.192+3362G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877221 | ||||||
| chr16:89877260
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+3401A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877260 | ||||||
| chr16:89877343
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.192+3484A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877343 | ||||||
| chr16:89877395
|
A | C | 1 | a0002c0003t0001g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.192+3536A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877395 | ||||||
| chr16:89877658
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.192+3799A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877658 | ||||||
| chr16:89877687
|
G | A | 21 | a0001c0001t0001g0291a0001c0001t0003g0292a0002c0003t0001g0005others(18): Show | 22 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.192+3828G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877687 | ||||||
| chr16:89877768
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.192+3909C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877768 | ||||||
| chr16:89877801
|
A | G | 3 | a0001c0001t0001g0264a0002c0003t0001g0052a0002c0003t0001g0053 | 3 | HG00099.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.192+3942A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877801 | ||||||
| chr16:89877835
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192+3976G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877835 | ||||||
| chr16:89877849
|
T | A | 1 | a0002c0003t0001g0277 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.192+3990T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877849 | ||||||
| chr16:89877922
|
T | C | 22 | a0001c0001t0001g0291a0001c0001t0003g0292a0002c0003t0001g0005others(19): Show | 23 | HG00639.hp1 HG01167.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+4063T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89877922 | ||||||
| chr16:89878172
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.192+4313C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878172 | ||||||
| chr16:89878278
|
TC | T | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+4420delC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878278 | ||||||
| chr16:89878279
|
C | CA | 21 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(18): Show | 21 | HG01109.hp1 HG01192.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.192+4434dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89878279 | |||||
| chr16:89878279
|
CA | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0218a0001c0001t0001g0265others(7): Show | 10 | HG01256.hp1 HG02486.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+4434delA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89878279 | |||||
| chr16:89878280
|
A | G | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+4421A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878280 | ||||||
| chr16:89878305
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.192+4446G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878305 | ||||||
| chr16:89878368
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.192+4509C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878368 | ||||||
| chr16:89878414
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0077others(8): Show | 12 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+4555C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878414 | ||||||
| chr16:89878434
|
A | AT | 84 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0057others(81): Show | 85 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.192+4599dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89878434 | |||||
| chr16:89878434
|
A | ATT | 18 | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0090others(15): Show | 18 | HG01106.hp2 HG01123.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+4598_192+4599d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89878434 | |||||
| chr16:89878434
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.192+4575A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878434 | ||||||
| chr16:89878434
|
AT | A | 46 | a0001c0001t0001g0197a0001c0001t0001g0265a0001c0001t0003g0292others(43): Show | 47 | HG00323.hp1 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.192+4599delT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89878434 | |||||
| chr16:89878434
|
ATT | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4598_192+4599d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89878434 | |||||
| chr16:89878437
|
T | A | 1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.192+4578T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878437 | ||||||
| chr16:89878732
|
C | T | 2 | a0001c0004t0002g0071a0001c0004t0002g0263 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.193-4619C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878732 | ||||||
| chr16:89878797
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.193-4554C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878797 | ||||||
| chr16:89878856
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0189 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.193-4495T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878856 | ||||||
| chr16:89878960
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.193-4391C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878960 | ||||||
| chr16:89878961
|
G | A | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-4390G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89878961 | ||||||
| chr16:89879017
|
G | C | 1 | a0001c0004t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-4334G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879017 | ||||||
| chr16:89879054
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-4297G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879054 | ||||||
| chr16:89879054
|
GGCCTGTC others(35): Show |
G | 1 | a0001c0001t0001g0151 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193-4287_193-4246d others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879054 | |||||
| chr16:89879066
|
G | A | 23 | a0001c0001t0001g0291a0001c0001t0003g0292a0002c0003t0001g0005others(20): Show | 24 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.193-4285G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879066 | ||||||
| chr16:89879100
|
T | C | 25 | a0001c0001t0001g0264a0001c0001t0001g0291a0001c0001t0003g0292others(22): Show | 26 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.193-4251T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879100 | ||||||
| chr16:89879136
|
GGGGCCTG others(203): Show |
G | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-4204_193-3995d others(2): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879136 | |||||
| chr16:89879205
|
ACACAGAT others(623): Show |
A | 1 | a0001c0001t0001g0247 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.193-4087_193-3458d others(2): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879205 | |||||
| chr16:89879254
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0146 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.193-4097T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879254 | ||||||
| chr16:89879296
|
C | T | 92 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 93 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.193-4055C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879296 | ||||||
| chr16:89879305
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0074others(31): Show | 35 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.193-4046G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879305 | ||||||
| chr16:89879315
|
C | T | 92 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 93 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.193-4036C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879315 | ||||||
| chr16:89879321
|
CTG | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.193-4028_193-4027d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879321 | |||||
| chr16:89879325
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0074others(31): Show | 35 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.193-4026T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879325 | ||||||
| chr16:89879344
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(2): Show | 5 | HG02258.hp1 HG02280.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-4007C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879344 | ||||||
| chr16:89879363
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3988C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879363 | ||||||
| chr16:89879390
|
A | G | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3961A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879390 | ||||||
| chr16:89879390
|
AGCCTGTC others(35): Show |
A | 3 | a0001c0001t0001g0057a0001c0004t0002g0071a0001c0004t0002g0263 | 3 | HG01993.hp2 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.193-3894_193-3853d others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879390 | |||||
| chr16:89879399
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3952C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879399 | ||||||
| chr16:89879405
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3946T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879405 | ||||||
| chr16:89879409
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3942C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879409 | ||||||
| chr16:89879415
|
A | ACACAGAT others(35): Show |
1 | a0001c0001t0001g0076 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.193-3895_193-3894i others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879415 | |||||
| chr16:89879415
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0084others(8): Show | 12 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.193-3936A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879415 | ||||||
| chr16:89879418
|
C | G | 19 | a0002c0003t0001g0005a0002c0003t0001g0191a0002c0003t0001g0274others(16): Show | 20 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.193-3933C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879418 | ||||||
| chr16:89879422
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3929T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879422 | ||||||
| chr16:89879428
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3923T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879428 | ||||||
| chr16:89879430
|
G | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3921G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879430 | ||||||
| chr16:89879437
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3914G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879437 | ||||||
| chr16:89879442
|
A | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3909A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879442 | ||||||
| chr16:89879447
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3904T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879447 | ||||||
| chr16:89879453
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0003g0292 | 2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.193-3898G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879453 | ||||||
| chr16:89879457
|
A | ACACAGAT others(35): Show |
4 | a0001c0001t0001g0112a0001c0001t0001g0137a0001c0001t0001g0156others(1): Show | 4 | HG03239.hp1 HG04228.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-3499_193-3458d others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879457 | |||||
| chr16:89879457
|
A | ACACAGAT others(77): Show |
21 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.193-3541_193-3458d others(86): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879457 | |||||
| chr16:89879457
|
A | ACACAGAT others(119): Show |
1 | a0001c0001t0001g0094 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.193-3583_193-3458d others(128): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879457 | |||||
| chr16:89879457
|
A | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0076others(10): Show | 14 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.193-3894A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879457 | ||||||
| chr16:89879457
|
ACACAGAT others(35): Show |
A | 25 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0098others(22): Show | 25 | HG00099.hp2 HG00733.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.193-3499_193-3458d others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879457 | |||||
| chr16:89879457
|
ACACAGAT others(77): Show |
A | 2 | a0001c0001t0001g0291a0007c0008t0001g0056 | 2 | HG02451.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.193-3541_193-3458d others(86): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879457 | |||||
| chr16:89879457
|
ACACAGAT others(203): Show |
A | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-3667_193-3458d others(2): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879457 | |||||
| chr16:89879499
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193-3852G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879499 | ||||||
| chr16:89879516
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.193-3835G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879516 | ||||||
| chr16:89879521
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.193-3830G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879521 | ||||||
| chr16:89879528
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-3823G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879528 | ||||||
| chr16:89879541
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3810G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879541 | ||||||
| chr16:89879554
|
T | TCGGGGCC others(77): Show |
1 | a0001c0001t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.193-3714_193-3713i others(86): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879554 | |||||
| chr16:89879556
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3795G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879556 | ||||||
| chr16:89879558
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3793G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879558 | ||||||
| chr16:89879567
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3784C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879567 | ||||||
| chr16:89879573
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3778T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879573 | ||||||
| chr16:89879573
|
T | TTGTCCGT others(77): Show |
17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.193-3754_193-3753i others(86): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879573 | |||||
| chr16:89879577
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3774C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879577 | ||||||
| chr16:89879579
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-3772G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879579 | ||||||
| chr16:89879583
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3768G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879583 | ||||||
| chr16:89879590
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3761T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879590 | ||||||
| chr16:89879596
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3755T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879596 | ||||||
| chr16:89879598
|
G | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3753G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879598 | ||||||
| chr16:89879612
|
G | A | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.193-3739G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879612 | ||||||
| chr16:89879615
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3736T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879615 | ||||||
| chr16:89879625
|
G | A | 9 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(6): Show | 9 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-3726G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879625 | ||||||
| chr16:89879628
|
C | G | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.193-3723C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879628 | ||||||
| chr16:89879642
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.193-3709G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879642 | ||||||
| chr16:89879654
|
G | A | 1 | a0001c0004t0002g0065 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-3697G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879654 | ||||||
| chr16:89879667
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3684G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879667 | ||||||
| chr16:89879696
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0169 | 2 | HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.193-3655G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879696 | ||||||
| chr16:89879709
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3642G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879709 | ||||||
| chr16:89879726
|
G | A | 32 | a0001c0001t0001g0245a0001c0001t0003g0292a0001c0002t0001g0021others(29): Show | 32 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.193-3625G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879726 | ||||||
| chr16:89879751
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 36 | HG00099.hp2 HG01109.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.193-3600G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879751 | ||||||
| chr16:89879766
|
G | GGGGCCTG others(35): Show |
1 | a0001c0001t0001g0224 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.193-3544_193-3543i others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879766 | |||||
| chr16:89879768
|
G | A | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-3583G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879768 | ||||||
| chr16:89879810
|
GGCCTGTC others(77): Show |
G | 15 | a0002c0003t0001g0005a0002c0003t0001g0275a0002c0003t0001g0276others(12): Show | 16 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.193-3516_193-3433d others(86): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879810 | |||||
| chr16:89879852
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 137 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.193-3499G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879852 | ||||||
| chr16:89879852
|
G | GGCCTGTC others(35): Show |
8 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0175others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-3474_193-3433d others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879852 | |||||
| chr16:89879852
|
GGCCTGTC others(35): Show |
G | 16 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0084others(13): Show | 17 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.193-3474_193-3433d others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89879852 | |||||
| chr16:89879873
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.193-3478G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879873 | ||||||
| chr16:89879884
|
T | C | 3 | a0001c0001t0001g0118a0001c0001t0001g0178a0001c0001t0001g0198 | 3 | NA18949.hp2 NA18971.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.193-3467T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879884 | ||||||
| chr16:89879892
|
G | A | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-3459G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879892 | ||||||
| chr16:89879894
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0083others(6): Show | 9 | HG00642.hp1 HG01074.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-3457A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879894 | ||||||
| chr16:89879919
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0109 | 2 | HG01243.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.193-3432A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879919 | ||||||
| chr16:89879927
|
A | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0077others(30): Show | 34 | HG00099.hp2 HG00741.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.193-3424A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879927 | ||||||
| chr16:89879972
|
A | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.193-3379A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879972 | ||||||
| chr16:89879980
|
A | C | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-3371A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879980 | ||||||
| chr16:89879981
|
C | G | 1 | a0001c0001t0001g0239 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.193-3370C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879981 | ||||||
| chr16:89879983
|
A | G | 24 | a0001c0001t0001g0264a0001c0001t0001g0291a0001c0001t0003g0292others(21): Show | 25 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.193-3368A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879983 | ||||||
| chr16:89879987
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.193-3364C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879987 | ||||||
| chr16:89879989
|
C | T | 1 | a0002c0003t0001g0280 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193-3362C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879989 | ||||||
| chr16:89879999
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.193-3352A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89879999 | ||||||
| chr16:89880103
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.193-3248G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880103 | ||||||
| chr16:89880124
|
TGTGTACA others(35): Show |
T | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-3214_193-3173d others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89880124 | |||||
| chr16:89880155
|
C | T | 21 | a0001c0001t0001g0291a0001c0001t0003g0292a0002c0003t0001g0005others(18): Show | 22 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.193-3196C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880155 | ||||||
| chr16:89880241
|
C | A | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-3110C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880241 | ||||||
| chr16:89880274
|
A | G | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-3077A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880274 | ||||||
| chr16:89880320
|
A | C | 19 | a0002c0003t0001g0005a0002c0003t0001g0191a0002c0003t0001g0274others(16): Show | 20 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.193-3031A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880320 | ||||||
| chr16:89880355
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.193-2996G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880355 | ||||||
| chr16:89880565
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.193-2786C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880565 | ||||||
| chr16:89880591
|
G | GA | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG01192.hp2 HG02145.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.193-2748dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89880591 | |||||
| chr16:89880613
|
G | A | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.193-2738G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880613 | ||||||
| chr16:89880623
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-2728G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880623 | ||||||
| chr16:89880795
|
G | A | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-2556G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880795 | ||||||
| chr16:89880798
|
G | C | 1 | a0001c0002t0001g0035 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.193-2553G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880798 | ||||||
| chr16:89880829
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.193-2522A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89880829 | ||||||
| chr16:89881037
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 11 | HG00733.hp1 HG01071.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-2314C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881037 | ||||||
| chr16:89881049
|
A | G | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-2302A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881049 | ||||||
| chr16:89881070
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0177 | 2 | HG01071.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.193-2281A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881070 | ||||||
| chr16:89881257
|
A | T | 2 | a0001c0001t0001g0272a0001c0005t0004g0271 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.193-2094A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881257 | ||||||
| chr16:89881299
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.193-2052C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881299 | ||||||
| chr16:89881415
|
A | G | 1 | a0001c0002t0001g0035 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.193-1936A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881415 | ||||||
| chr16:89881453
|
T | A | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-1898T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881453 | ||||||
| chr16:89881454
|
A | T | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.193-1897A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881454 | ||||||
| chr16:89881508
|
T | A | 1 | a0001c0002t0001g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.193-1843T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881508 | ||||||
| chr16:89881540
|
GGA | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.193-1810_193-1809d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881540 | ||||||
| chr16:89881572
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.193-1779G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881572 | ||||||
| chr16:89881598
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.193-1753G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881598 | ||||||
| chr16:89881687
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-1664C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881687 | ||||||
| chr16:89881725
|
A | C | 1 | a0001c0001t0001g0244 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.193-1626A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881725 | ||||||
| chr16:89881762
|
T | G | 1 | a0001c0002t0001g0049 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.193-1589T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881762 | ||||||
| chr16:89881865
|
C | A | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.193-1486C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881865 | ||||||
| chr16:89881921
|
A | AT | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-1423dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89881921 | |||||
| chr16:89881954
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.193-1397C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881954 | ||||||
| chr16:89881989
|
G | A | 59 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 59 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.193-1362G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89881989 | ||||||
| chr16:89882036
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 111 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.193-1315C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882036 | ||||||
| chr16:89882039
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.193-1312C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882039 | ||||||
| chr16:89882053
|
G | A | 1 | a0009c0013t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-1298G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882053 | ||||||
| chr16:89882175
|
C | T | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.193-1176C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882175 | ||||||
| chr16:89882260
|
C | T | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.193-1091C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882260 | ||||||
| chr16:89882310
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.193-1041G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882310 | ||||||
| chr16:89882443
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.193-908C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882443 | ||||||
| chr16:89882540
|
A | AAG | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-801_193-800dup others(2): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89882540 | |||||
| chr16:89882577
|
A | G | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-774A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882577 | ||||||
| chr16:89882592
|
G | C | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.193-759G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882592 | ||||||
| chr16:89882600
|
A | G | 5 | a0002c0003t0001g0276a0002c0003t0001g0278a0002c0003t0001g0279others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-751A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882600 | ||||||
| chr16:89882608
|
A | T | 2 | a0001c0001t0001g0098a0001c0004t0002g0061 | 2 | HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.193-743A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882608 | ||||||
| chr16:89882625
|
T | C | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.193-726T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882625 | ||||||
| chr16:89882784
|
G | A | 2 | a0001c0001t0001g0062a0001c0004t0002g0063 | 2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.193-567G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882784 | ||||||
| chr16:89882797
|
G | A | 40 | a0001c0001t0001g0054a0001c0001t0001g0245a0001c0001t0001g0265others(37): Show | 40 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.193-554G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89882797 | ||||||
| chr16:89883116
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.193-235C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89883116 | ||||||
| chr16:89883156
|
C | CA | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.193-192dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 89883156 | |||||
| chr16:89883205
|
G | A | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.193-146G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 1/17 | chr16 | 89883205 | ||||||
| chr16:89883518
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA19088.hp1 | splice_region_variant&intron_variant | LOW | c.354+6G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89883518 | ||||||
| chr16:89883548
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.354+36G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89883548 | ||||||
| chr16:89883758
|
A | ACACGTGT others(20): Show |
2 | a0001c0001t0001g0272a0001c0005t0004g0271 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.354+267_354+293dup others(27): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 89883758 | |||||
| chr16:89883768
|
C | CCCTCCTA others(47): Show |
2 | a0001c0001t0001g0219a0001c0001t0001g0227 | 2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.354+267_354+320dup others(54): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 89883768 | |||||
| chr16:89883768
|
CCCTCCTA others(47): Show |
C | 1 | a0001c0001t0001g0015 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.354+267_354+320del others(54): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 89883768 | |||||
| chr16:89883779
|
A | AACCGCGC others(47): Show |
5 | a0001c0001t0001g0164a0001c0001t0001g0189a0001c0001t0001g0261others(2): Show | 5 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+309_354+310ins others(54): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 89883779 | |||||
| chr16:89883779
|
AACCGCGC others(20): Show |
A | 2 | a0001c0001t0001g0078a0001c0001t0001g0101 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.354+283_354+309del others(27): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 89883779 | |||||
| chr16:89883779
|
AACCGCGC others(47): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.354+285_354+338del others(54): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 89883779 | |||||
| chr16:89883795
|
CCCTCCTA others(20): Show |
C | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | HG01109.hp1 HG01167.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.354+310_354+336del others(27): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 89883795 | |||||
| chr16:89883822
|
G | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0099others(73): Show | 77 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.354+310G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89883822 | ||||||
| chr16:89883839
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354+327G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89883839 | ||||||
| chr16:89883891
|
G | C | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.354+379G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89883891 | ||||||
| chr16:89884149
|
A | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 80 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.355-433A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884149 | ||||||
| chr16:89884211
|
G | A | 1 | a0002c0006t0002g0182 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.355-371G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884211 | ||||||
| chr16:89884301
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.355-281G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884301 | ||||||
| chr16:89884303
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.355-279C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884303 | ||||||
| chr16:89884304
|
G | A | 5 | a0002c0003t0001g0276a0002c0003t0001g0278a0002c0003t0001g0279others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-278G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884304 | ||||||
| chr16:89884310
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.355-272G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884310 | ||||||
| chr16:89884331
|
T | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(77): Show | 81 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.355-251T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884331 | ||||||
| chr16:89884406
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.355-176C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884406 | ||||||
| chr16:89884493
|
G | A | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.355-89G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884493 | ||||||
| chr16:89884509
|
G | A | 2 | a0001c0004t0002g0066a0001c0004t0002g0069 | 2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.355-73G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884509 | ||||||
| chr16:89884574
|
A | G | 23 | a0001c0001t0001g0264a0001c0001t0003g0292a0002c0003t0001g0005others(20): Show | 24 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.355-8A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 2/17 | chr16 | 89884574 | ||||||
| chr16:89884685
|
G | GTCCCTCT others(34): Show |
1 | a0001c0001t0001g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.429+48_429+88dupCT others(39): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884685 | |||||
| chr16:89884720
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.429+64C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884720 | ||||||
| chr16:89884721
|
G | GCCCCTCT others(200): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0051 | 3 | HG01109.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.429+68_429+69insCT others(205): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884721 | |||||
| chr16:89884721
|
G | GCCCCTCT others(281): Show |
1 | a0001c0001t0001g0012 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+68_429+69insCT others(286): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884721 | |||||
| chr16:89884721
|
G | GCCCCTCT others(301): Show |
11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(8): Show | 11 | HG01192.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+68_429+69insCT others(306): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884721 | |||||
| chr16:89884721
|
G | GCCCCTCT others(301): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0011 | 2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.429+68_429+69insCT others(306): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884721 | |||||
| chr16:89884721
|
G | GCCCCTCT others(280): Show |
1 | a0001c0001t0001g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.429+68_429+69insCT others(285): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884721 | |||||
| chr16:89884721
|
G | GCCCTCTC others(55): Show |
15 | a0002c0003t0001g0005a0002c0003t0001g0275a0002c0003t0001g0276others(12): Show | 16 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.429+88_429+89insCT others(60): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884721 | |||||
| chr16:89884740
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.429+84C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884740 | ||||||
| chr16:89884741
|
G | GCCCCTCT others(35): Show |
7 | a0001c0001t0001g0264a0002c0003t0001g0052a0002c0003t0001g0053others(4): Show | 7 | HG00099.hp2 HG03471.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+88_429+89insCT others(40): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884741 | |||||
| chr16:89884750
|
C | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0051 | 3 | HG01109.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.429+94C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884750 | ||||||
| chr16:89884755
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.429+99T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884755 | ||||||
| chr16:89884770
|
C | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0051others(18): Show | 21 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.429+114C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884770 | ||||||
| chr16:89884781
|
G | GC | 31 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 32 | HG00639.hp1 HG01167.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.429+128dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884781 | |||||
| chr16:89884781
|
G | GCCCTCTC others(14): Show |
15 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(12): Show | 15 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.429+133_429+134ins others(21): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884781 | |||||
| chr16:89884790
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0051others(1): Show | 4 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+134C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884790 | ||||||
| chr16:89884801
|
G | GC | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(21): Show | 24 | HG00099.hp2 HG01192.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.429+148dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884801 | |||||
| chr16:89884810
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0051 | 2 | HG01109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.429+154C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884810 | ||||||
| chr16:89884821
|
G | GC | 18 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0051others(15): Show | 18 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.429+168dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884821 | |||||
| chr16:89884825
|
TCTCCCTC others(11): Show |
T | 1 | a0001c0002t0001g0049 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.429+174_429+191del others(18): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884825 | |||||
| chr16:89884830
|
C | G | 30 | a0001c0001t0001g0245a0001c0001t0001g0291a0001c0002t0001g0021others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.429+174C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884830 | ||||||
| chr16:89884830
|
CTCTGTCT others(11): Show |
C | 2 | a0001c0005t0001g0266a0001c0005t0001g0268 | 2 | NA18951.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.429+179_429+196del others(18): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884830 | |||||
| chr16:89884835
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.429+179T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884835 | ||||||
| chr16:89884840
|
C | T | 1 | a0001c0004t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.429+184C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884840 | ||||||
| chr16:89884843
|
C | CCCTCTCC others(56): Show |
1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.429+188_429+189ins others(63): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884843
|
C | CCT | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 88 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.429+189_429+190dup others(2): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884843
|
C | CCTCTCCC others(625): Show |
1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429+190_429+191ins others(632): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884843
|
C | CCTCTCCC others(623): Show |
1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.429+190_429+191ins others(630): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884843
|
C | CCTCTCCC others(623): Show |
1 | a0001c0005t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.429+190_429+191ins others(630): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884843
|
C | CCTCTCCC others(785): Show |
1 | a0001c0001t0001g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.429+190_429+191ins others(792): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884843
|
C | CCTCTCCC others(703): Show |
1 | a0001c0005t0004g0271 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.429+190_429+191ins others(710): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884843
|
C | CCTCTCCG others(15): Show |
1 | a0001c0002t0001g0024 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.429+190_429+191ins others(22): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884843 | |||||
| chr16:89884848
|
G | C | 23 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0051others(20): Show | 23 | HG00099.hp2 HG01109.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.429+192G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884848 | ||||||
| chr16:89884853
|
C | T | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.429+197C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884853 | ||||||
| chr16:89884859
|
G | GC | 20 | a0001c0001t0001g0014a0001c0001t0003g0292a0001c0002t0001g0025others(17): Show | 21 | HG00639.hp1 HG01167.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.429+206dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884859 | |||||
| chr16:89884859
|
GCCCTCTC others(14): Show |
G | 3 | a0001c0001t0001g0131a0001c0001t0001g0155a0001c0001t0001g0235 | 3 | HG01074.hp2 HG01433.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.429+248_429+268del others(21): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884859 | |||||
| chr16:89884863
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.429+207T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884863 | ||||||
| chr16:89884864
|
C | A | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG00099.hp1 HG00735.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+208C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884864 | ||||||
| chr16:89884868
|
C | G | 9 | a0001c0001t0001g0264a0001c0002t0001g0045a0001c0004t0002g0097others(6): Show | 9 | HG00099.hp2 HG00621.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+212C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884868 | ||||||
| chr16:89884879
|
GC | G | 20 | a0001c0001t0001g0098a0001c0001t0001g0270a0001c0004t0002g0058others(17): Show | 20 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.429+227delC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884879 | |||||
| chr16:89884880
|
C | CCCCTCTC others(13): Show |
15 | a0002c0003t0001g0005a0002c0003t0001g0275a0002c0003t0001g0276others(12): Show | 16 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.429+228_429+247dup others(20): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884880 | |||||
| chr16:89884880
|
C | CCCCTCTC others(640): Show |
1 | a0001c0005t0001g0266 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.429+308_429+309ins others(647): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884880 | |||||
| chr16:89884880
|
C | CCCCTCTC others(640): Show |
1 | a0001c0005t0001g0268 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(647): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884880 | |||||
| chr16:89884880
|
C | CCCTCTCC others(516): Show |
1 | a0001c0001t0001g0272 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.429+226_429+227ins others(523): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884880 | |||||
| chr16:89884880
|
C | CCCTCTCC others(517): Show |
1 | a0005c0007t0001g0047 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.429+226_429+227ins others(524): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884880 | |||||
| chr16:89884900
|
GC | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(32): Show | 35 | HG01192.hp2 HG01891.hp2 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.429+248delC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884900 | |||||
| chr16:89884901
|
C | A | 1 | a0001c0004t0002g0070 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.429+245C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884901 | ||||||
| chr16:89884901
|
C | CCCCTCTC others(54): Show |
1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.429+288_429+289ins others(61): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884901 | |||||
| chr16:89884901
|
C | CCCCTCTC others(558): Show |
4 | a0001c0002t0001g0023a0001c0002t0001g0032a0001c0002t0001g0033others(1): Show | 4 | HG02129.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+308_429+309ins others(565): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884901 | |||||
| chr16:89884901
|
C | CCCCTCTC others(578): Show |
1 | a0001c0002t0001g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(585): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884901 | |||||
| chr16:89884901
|
C | CCCCTCTC others(558): Show |
1 | a0001c0002t0001g0029 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.429+308_429+309ins others(565): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884901 | |||||
| chr16:89884901
|
C | CCCTCTCC others(153): Show |
1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.429+247_429+248ins others(160): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884901 | |||||
| chr16:89884901
|
C | CCCTCTCC others(537): Show |
1 | a0001c0002t0001g0025 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.429+247_429+248ins others(544): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884901 | |||||
| chr16:89884920
|
C | T | 14 | a0001c0001t0001g0098a0001c0004t0002g0059a0001c0004t0002g0061others(11): Show | 14 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.429+264C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884920 | ||||||
| chr16:89884922
|
CCCTCTCC others(73): Show |
C | 1 | a0001c0004t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.429+269_429+348del others(80): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884922 | |||||
| chr16:89884930
|
C | CTCTGCCT others(13): Show |
1 | a0001c0001t0001g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.429+293_429+294ins others(20): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884930 | |||||
| chr16:89884941
|
G | GC | 8 | a0001c0001t0001g0291a0001c0001t0003g0292a0002c0003t0001g0052others(5): Show | 8 | HG02451.hp2 HG03471.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+288dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884941 | |||||
| chr16:89884941
|
G | GCCCTCTC others(579): Show |
1 | a0001c0002t0001g0035 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(586): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884941 | |||||
| chr16:89884941
|
G | GCCCTCTC others(14): Show |
1 | a0001c0001t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+293_429+294ins others(21): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884941 | |||||
| chr16:89884961
|
GC | G | 35 | a0001c0001t0001g0019a0001c0001t0001g0098a0001c0001t0001g0264others(32): Show | 36 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.429+309delC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884961 | |||||
| chr16:89884962
|
C | CCCTCTCC others(598): Show |
1 | a0001c0002t0001g0048 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(605): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(32): Show |
4 | a0002c0003t0001g0191a0002c0003t0001g0274a0002c0003t0001g0277others(1): Show | 4 | HG03688.hp1 HG04115.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+308_429+309ins others(39): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(558): Show |
1 | a0001c0002t0001g0043 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(565): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(558): Show |
1 | a0003c0014t0001g0026 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(565): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(558): Show |
1 | a0001c0002t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(565): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(52): Show |
1 | a0002c0003t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.429+308_429+309ins others(59): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(558): Show |
1 | a0001c0002t0001g0022 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(565): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(578): Show |
3 | a0001c0002t0001g0021a0001c0002t0001g0024a0001c0002t0001g0040 | 3 | HG00673.hp2 HG02165.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.429+308_429+309ins others(585): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(477): Show |
1 | a0001c0002t0001g0042 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(484): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(578): Show |
7 | a0001c0001t0001g0245a0001c0002t0001g0030a0001c0002t0001g0031others(4): Show | 7 | HG00597.hp2 HG02015.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+308_429+309ins others(585): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(578): Show |
2 | a0001c0002t0001g0049a0001c0002t0001g0050 | 2 | HG00621.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.429+308_429+309ins others(585): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(578): Show |
1 | a0001c0002t0001g0044 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.429+308_429+309ins others(585): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(578): Show |
2 | a0001c0002t0001g0028a0001c0002t0001g0039 | 2 | NA18952.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.429+308_429+309ins others(585): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(578): Show |
1 | a0001c0002t0001g0046 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(585): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884962
|
C | CCCTCTCC others(72): Show |
1 | a0002c0003t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.429+308_429+309ins others(79): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884962 | |||||
| chr16:89884976
|
T | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+320T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884976 | ||||||
| chr16:89884982
|
G | GC | 17 | a0001c0001t0001g0019a0001c0001t0001g0098a0001c0001t0003g0292others(14): Show | 17 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.429+329dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884982 | |||||
| chr16:89884982
|
G | GCCCTCTC others(155): Show |
1 | a0002c0003t0001g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.429+334_429+335ins others(162): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884982 | |||||
| chr16:89884982
|
G | GCCCTCTC others(175): Show |
11 | a0002c0003t0001g0005a0002c0003t0001g0191a0002c0003t0001g0277others(8): Show | 12 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+334_429+335ins others(182): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884982 | |||||
| chr16:89884982
|
G | GCCCTCTC others(195): Show |
1 | a0002c0003t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.429+334_429+335ins others(202): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89884982 | |||||
| chr16:89884991
|
G | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+335G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89884991 | ||||||
| chr16:89885002
|
G | GC | 16 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(13): Show | 16 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.429+349dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885002 | |||||
| chr16:89885002
|
G | GCCCCTCT others(77): Show |
1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.429+349_429+350ins others(84): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885002 | |||||
| chr16:89885002
|
G | GCCCTCTC others(115): Show |
1 | a0002c0003t0001g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.429+389_429+390ins others(122): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885002 | |||||
| chr16:89885002
|
G | GCCCTCTC others(155): Show |
2 | a0002c0003t0001g0278a0002c0003t0001g0284 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.429+389_429+390ins others(162): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885002 | |||||
| chr16:89885002
|
G | GCCCTCTC others(175): Show |
2 | a0002c0003t0001g0276a0002c0003t0001g0280 | 2 | HG01167.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.429+389_429+390ins others(182): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885002 | |||||
| chr16:89885042
|
GC | G | 32 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(29): Show | 32 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.429+390delC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885042 | |||||
| chr16:89885043
|
C | CCCTCTCC others(54): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(3): Show | 6 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+389_429+390ins others(61): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885043 | |||||
| chr16:89885043
|
C | CCCTCTCC others(155): Show |
1 | a0001c0001t0001g0019 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.429+389_429+390ins others(162): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885043 | |||||
| chr16:89885043
|
CCCCTCTC others(33): Show |
C | 1 | a0001c0001t0001g0234 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.429+429_429+468del others(40): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885043 | |||||
| chr16:89885052
|
C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(31): Show | 35 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.429+396C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885052 | ||||||
| chr16:89885063
|
G | GC | 11 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(8): Show | 11 | HG01192.hp2 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+410dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885063 | |||||
| chr16:89885072
|
C | G | 19 | a0001c0001t0003g0292a0002c0003t0001g0005a0002c0003t0001g0191others(16): Show | 20 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.429+416C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885072 | ||||||
| chr16:89885083
|
G | GC | 3 | a0001c0001t0001g0264a0002c0003t0001g0052a0002c0003t0001g0053 | 3 | HG00099.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.429+430dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885083 | |||||
| chr16:89885092
|
C | CTCTGCCT others(136): Show |
1 | a0002c0003t0001g0279 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.429+468_429+469ins others(143): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885092 | |||||
| chr16:89885102
|
C | CGCCCTCT others(13): Show |
1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.429+465_429+466ins others(20): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885102 | |||||
| chr16:89885102
|
C | T | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(50): Show | 53 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.429+446C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885102 | ||||||
| chr16:89885103
|
G | GC | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(34): Show | 37 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.429+450dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCCTCT others(445): Show |
1 | a0001c0005t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.429+450_429+451ins others(452): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCCTCT others(445): Show |
2 | a0001c0005t0001g0266a0001c0005t0001g0268 | 2 | NA18951.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.429+450_429+451ins others(452): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCCTCT others(384): Show |
1 | a0001c0005t0004g0271 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.429+450_429+451ins others(391): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(466): Show |
1 | a0001c0001t0001g0272 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.429+468_429+469ins others(473): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(464): Show |
1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.429+468_429+469ins others(471): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(443): Show |
1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.429+468_429+469ins others(450): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(156): Show |
1 | a0001c0001t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+468_429+469ins others(163): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(240): Show |
1 | a0001c0001t0001g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.429+468_429+469ins others(247): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(116): Show |
1 | a0001c0001t0001g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.429+468_429+469ins others(123): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(74): Show |
1 | a0001c0001t0001g0014 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.429+468_429+469ins others(81): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(54): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0013others(5): Show | 8 | HG00323.hp1 HG02280.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+468_429+469ins others(61): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(34): Show |
1 | a0001c0001t0001g0012 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+468_429+469ins others(41): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885103
|
G | GCCCTCTC others(13): Show |
1 | a0002c0003t0001g0279 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.429+466_429+467ins others(20): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 89885103 | |||||
| chr16:89885191
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.429+535C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885191 | ||||||
| chr16:89885305
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.430-543G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885305 | ||||||
| chr16:89885424
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430-424A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885424 | ||||||
| chr16:89885475
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.430-373A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885475 | ||||||
| chr16:89885478
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.430-370T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885478 | ||||||
| chr16:89885574
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.430-274T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885574 | ||||||
| chr16:89885637
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.430-211G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885637 | ||||||
| chr16:89885663
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-185G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885663 | ||||||
| chr16:89885712
|
A | C | 1 | a0001c0002t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.430-136A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885712 | ||||||
| chr16:89885761
|
C | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-87C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 3/17 | chr16 | 89885761 | ||||||
| chr16:89885977
|
C | CGCCCTTC others(9): Show |
44 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(41): Show | 45 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.548+71_548+86dupCG others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89885977 | |||||
| chr16:89885977
|
C | CGCCCTTC others(25): Show |
15 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.548+55_548+86dupCG others(30): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89885977 | |||||
| chr16:89885977
|
C | CGCCCTTC others(41): Show |
1 | a0001c0004t0002g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.548+39_548+86dupCG others(46): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89885977 | |||||
| chr16:89885977
|
C | CGCCCTTC others(9): Show |
8 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0270others(5): Show | 8 | HG00099.hp2 HG03239.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.548+22_548+23insTG others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89885977 | |||||
| chr16:89885977
|
C | CGCCCTTC others(25): Show |
18 | a0001c0001t0003g0292a0001c0002t0001g0021a0001c0002t0001g0035others(15): Show | 18 | HG00609.hp1 HG00639.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.548+22_548+23insTG others(30): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89885977 | |||||
| chr16:89885977
|
C | CGCCCTTC others(41): Show |
35 | a0001c0001t0001g0245a0001c0002t0001g0022a0001c0002t0001g0023others(32): Show | 36 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.548+22_548+23insTG others(46): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89885977 | |||||
| chr16:89885977
|
CGCCCTTC others(9): Show |
C | 4 | a0001c0001t0001g0130a0001c0001t0001g0145a0001c0001t0001g0154others(1): Show | 4 | HG00639.hp2 NA18952.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.548+71_548+86delCG others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89885977 | |||||
| chr16:89885989
|
C | T | 2 | a0001c0001t0001g0291a0001c0005t0004g0271 | 2 | HG02451.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.548+23C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89885989 | ||||||
| chr16:89886013
|
C | CTTCTCTG others(25): Show |
1 | a0009c0013t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.548+78_548+79insGT others(30): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89886013 | |||||
| chr16:89886037
|
CGGCTGCC others(9): Show |
C | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.548+79_548+94delCT others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 89886037 | |||||
| chr16:89886053
|
T | C | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.548+87T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886053 | ||||||
| chr16:89886066
|
G | C | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.548+100G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886066 | ||||||
| chr16:89886279
|
T | G | 1 | a0001c0004t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.548+313T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886279 | ||||||
| chr16:89886435
|
T | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.548+469T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886435 | ||||||
| chr16:89886438
|
T | A | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.548+472T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886438 | ||||||
| chr16:89886658
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.548+692G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886658 | ||||||
| chr16:89886702
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.548+736C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886702 | ||||||
| chr16:89886763
|
A | G | 3 | a0001c0004t0002g0063a0001c0004t0002g0066a0001c0004t0002g0070 | 3 | HG02922.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.548+797A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886763 | ||||||
| chr16:89886810
|
G | A | 17 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.549-842G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886810 | ||||||
| chr16:89886926
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.549-726C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89886926 | ||||||
| chr16:89887139
|
T | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.549-513T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887139 | ||||||
| chr16:89887183
|
A | G | 1 | a0002c0006t0002g0182 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.549-469A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887183 | ||||||
| chr16:89887190
|
C | T | 1 | a0002c0003t0001g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.549-462C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887190 | ||||||
| chr16:89887216
|
C | G | 5 | a0001c0001t0001g0062a0001c0004t0002g0063a0001c0004t0002g0066others(2): Show | 5 | HG02145.hp1 HG02922.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.549-436C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887216 | ||||||
| chr16:89887255
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.549-397C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887255 | ||||||
| chr16:89887338
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.549-314G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887338 | ||||||
| chr16:89887365
|
A | G | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.549-287A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887365 | ||||||
| chr16:89887418
|
A | G | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.549-234A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887418 | ||||||
| chr16:89887502
|
G | A | 1 | a0001c0004t0002g0263 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.549-150G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 4/17 | chr16 | 89887502 | ||||||
| chr16:89887730
|
G | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.614+13G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89887730 | ||||||
| chr16:89888004
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.614+287G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888004 | ||||||
| chr16:89888036
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.614+319C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888036 | ||||||
| chr16:89888057
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.614+340G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888057 | ||||||
| chr16:89888070
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.614+353A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888070 | ||||||
| chr16:89888125
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.614+408C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888125 | ||||||
| chr16:89888140
|
TCTGTAAT others(316): Show |
T | 1 | a0001c0001t0001g0129 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.614+446_614+768del | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89888140 | |||||
| chr16:89888243
|
C | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 80 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.614+526C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888243 | ||||||
| chr16:89888244
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.614+527C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888244 | ||||||
| chr16:89888259
|
G | A | 2 | a0001c0001t0001g0137a0008c0011t0001g0120 | 2 | NA18983.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.614+542G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888259 | ||||||
| chr16:89888274
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.614+557G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888274 | ||||||
| chr16:89888351
|
G | T | 17 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.614+634G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888351 | ||||||
| chr16:89888433
|
C | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA19003.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.614+716C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888433 | ||||||
| chr16:89888496
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.614+779G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888496 | ||||||
| chr16:89888588
|
CA | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.614+885delA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89888588 | |||||
| chr16:89888604
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.614+887A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888604 | ||||||
| chr16:89888679
|
C | CT | 58 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.614+977dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89888679 | |||||
| chr16:89888683
|
T | C | 2 | a0001c0001t0001g0088a0001c0001t0001g0151 | 2 | HG02080.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.614+966T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888683 | ||||||
| chr16:89888757
|
A | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.614+1040A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888757 | ||||||
| chr16:89888798
|
C | T | 1 | a0002c0003t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.614+1081C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888798 | ||||||
| chr16:89888822
|
C | T | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.614+1105C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888822 | ||||||
| chr16:89888840
|
A | AT | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(70): Show | 73 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.614+1149dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89888840 | |||||
| chr16:89888840
|
A | ATT | 6 | a0001c0005t0004g0271a0002c0003t0001g0005a0002c0003t0001g0277others(3): Show | 7 | HG00639.hp1 HG02257.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.614+1148_614+1149d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89888840 | |||||
| chr16:89888840
|
AT | A | 15 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0002t0001g0041others(12): Show | 15 | HG01256.hp2 HG02055.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.614+1149delT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89888840 | |||||
| chr16:89888875
|
C | T | 21 | a0001c0001t0001g0264a0001c0001t0003g0292a0002c0003t0001g0005others(18): Show | 22 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.614+1158C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89888875 | ||||||
| chr16:89889027
|
G | A | 1 | a0001c0005t0001g0268 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.614+1310G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889027 | ||||||
| chr16:89889230
|
A | G | 17 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.614+1513A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889230 | ||||||
| chr16:89889268
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.614+1551C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889268 | ||||||
| chr16:89889269
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.614+1552G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889269 | ||||||
| chr16:89889287
|
C | T | 17 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.614+1570C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889287 | ||||||
| chr16:89889332
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA19003.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.614+1615C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889332 | ||||||
| chr16:89889483
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.614+1766A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889483 | ||||||
| chr16:89889639
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.614+1922C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889639 | ||||||
| chr16:89889809
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.614+2092C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889809 | ||||||
| chr16:89889810
|
G | A | 6 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0175others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.614+2093G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889810 | ||||||
| chr16:89889839
|
C | T | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.614+2122C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889839 | ||||||
| chr16:89889841
|
T | C | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.614+2124T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889841 | ||||||
| chr16:89889845
|
T | C | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.614+2128T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889845 | ||||||
| chr16:89889891
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.614+2174G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889891 | ||||||
| chr16:89889913
|
GCT | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.614+2199_614+2200d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89889913 | |||||
| chr16:89889921
|
G | C | 1 | a0001c0004t0002g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.614+2204G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889921 | ||||||
| chr16:89889964
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.615-2229G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89889964 | ||||||
| chr16:89890059
|
G | A | 1 | a0007c0008t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.615-2134G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890059 | ||||||
| chr16:89890095
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0161 | 2 | NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.615-2098C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890095 | ||||||
| chr16:89890105
|
A | C | 19 | a0002c0003t0001g0005a0002c0003t0001g0191a0002c0003t0001g0274others(16): Show | 20 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.615-2088A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890105 | ||||||
| chr16:89890135
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(4): Show | 7 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.615-2058G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890135 | ||||||
| chr16:89890208
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.615-1985C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890208 | ||||||
| chr16:89890298
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0003g0292 | 2 | HG00099.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.615-1895C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890298 | ||||||
| chr16:89890303
|
TCTGCAGG others(13): Show |
T | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1885_615-1866d others(22): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89890303 | |||||
| chr16:89890330
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1863A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890330 | ||||||
| chr16:89890360
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.615-1833G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890360 | ||||||
| chr16:89890368
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1825A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890368 | ||||||
| chr16:89890388
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1805A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890388 | ||||||
| chr16:89890403
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1790A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890403 | ||||||
| chr16:89890415
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1778T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890415 | ||||||
| chr16:89890439
|
G | GGAGTTTG others(15): Show |
1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1753_615-1752i others(24): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 89890439 | |||||
| chr16:89890441
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1752T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890441 | ||||||
| chr16:89890450
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1743C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890450 | ||||||
| chr16:89890454
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1739C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890454 | ||||||
| chr16:89890456
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1737T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890456 | ||||||
| chr16:89890457
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1736C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890457 | ||||||
| chr16:89890475
|
T | A | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1718T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890475 | ||||||
| chr16:89890477
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1716G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890477 | ||||||
| chr16:89890481
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1712T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890481 | ||||||
| chr16:89890487
|
T | C | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.615-1706T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890487 | ||||||
| chr16:89890504
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.615-1689A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890504 | ||||||
| chr16:89890621
|
C | G | 1 | a0001c0002t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.615-1572C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890621 | ||||||
| chr16:89890761
|
T | G | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.615-1432T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890761 | ||||||
| chr16:89890847
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0165others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.615-1346A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890847 | ||||||
| chr16:89890879
|
A | G | 1 | a0001c0002t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.615-1314A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890879 | ||||||
| chr16:89890903
|
A | G | 1 | a0001c0004t0002g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.615-1290A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89890903 | ||||||
| chr16:89891185
|
C | T | 1 | a0001c0002t0001g0031 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.615-1008C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891185 | ||||||
| chr16:89891227
|
T | C | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.615-966T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891227 | ||||||
| chr16:89891237
|
C | T | 1 | a0009c0013t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.615-956C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891237 | ||||||
| chr16:89891243
|
A | T | 1 | a0002c0003t0001g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.615-950A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891243 | ||||||
| chr16:89891298
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.615-895C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891298 | ||||||
| chr16:89891407
|
A | G | 101 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(98): Show | 102 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.615-786A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891407 | ||||||
| chr16:89891560
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.615-633T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891560 | ||||||
| chr16:89891710
|
G | A | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.615-483G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891710 | ||||||
| chr16:89891718
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.615-475G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891718 | ||||||
| chr16:89891719
|
T | C | 39 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(36): Show | 39 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.615-474T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891719 | ||||||
| chr16:89891739
|
C | T | 3 | a0002c0003t0001g0191a0002c0003t0001g0277a0002c0003t0001g0283 | 3 | HG03688.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.615-454C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891739 | ||||||
| chr16:89891760
|
T | C | 3 | a0002c0003t0001g0191a0002c0003t0001g0277a0002c0003t0001g0283 | 3 | HG03688.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.615-433T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891760 | ||||||
| chr16:89891785
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0003g0292 | 2 | HG00099.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.615-408G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891785 | ||||||
| chr16:89891810
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0003g0292 | 2 | HG00099.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.615-383A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891810 | ||||||
| chr16:89891814
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.615-379G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891814 | ||||||
| chr16:89891825
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0003g0292 | 2 | HG00099.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.615-368C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891825 | ||||||
| chr16:89891954
|
G | C | 1 | a0002c0003t0001g0279 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.615-239G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891954 | ||||||
| chr16:89891991
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0180 | 2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.615-202T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89891991 | ||||||
| chr16:89892013
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.615-180G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89892013 | ||||||
| chr16:89892066
|
C | A | 4 | a0002c0003t0001g0285a0002c0003t0001g0287a0002c0003t0001g0288others(1): Show | 4 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.615-127C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89892066 | ||||||
| chr16:89892130
|
G | A | 31 | a0001c0001t0001g0245a0001c0002t0001g0021a0001c0002t0001g0022others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.615-63G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89892130 | ||||||
| chr16:89892172
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.615-21C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 5/17 | chr16 | 89892172 | ||||||
| chr16:89892340
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.697+65G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892340 | ||||||
| chr16:89892500
|
C | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.697+225C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892500 | ||||||
| chr16:89892625
|
C | T | 1 | a0002c0003t0001g0286 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.697+350C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892625 | ||||||
| chr16:89892683
|
A | G | 5 | a0002c0003t0001g0276a0002c0003t0001g0278a0002c0003t0001g0279others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.697+408A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892683 | ||||||
| chr16:89892740
|
T | G | 1 | a0001c0005t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.697+465T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892740 | ||||||
| chr16:89892795
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.697+520C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892795 | ||||||
| chr16:89892953
|
G | C | 6 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG01256.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.697+678G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892953 | ||||||
| chr16:89892979
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG00099.hp2 HG01109.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.697+704A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89892979 | ||||||
| chr16:89893161
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.698-567C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893161 | ||||||
| chr16:89893239
|
A | G | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 79 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.698-489A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893239 | ||||||
| chr16:89893266
|
A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0001g0261others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-462A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893266 | ||||||
| chr16:89893397
|
G | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.698-331G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893397 | ||||||
| chr16:89893472
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.698-256C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893472 | ||||||
| chr16:89893480
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.698-248G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893480 | ||||||
| chr16:89893552
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.698-176C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893552 | ||||||
| chr16:89893610
|
T | C | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.698-118T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893610 | ||||||
| chr16:89893656
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.698-72G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 6/17 | chr16 | 89893656 | ||||||
| chr16:89893920
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.828+62C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89893920 | ||||||
| chr16:89893992
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.828+134G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89893992 | ||||||
| chr16:89894066
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.828+208C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894066 | ||||||
| chr16:89894084
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.828+226G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894084 | ||||||
| chr16:89894098
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.828+240C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894098 | ||||||
| chr16:89894134
|
C | T | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.828+276C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894134 | ||||||
| chr16:89894136
|
G | C | 2 | a0002c0003t0001g0275a0002c0003t0001g0281 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.828+278G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894136 | ||||||
| chr16:89894179
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.828+321C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894179 | ||||||
| chr16:89894210
|
C | T | 41 | a0001c0001t0001g0113a0001c0001t0001g0146a0001c0001t0001g0148others(38): Show | 42 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.828+352C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894210 | ||||||
| chr16:89894211
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0147a0001c0001t0001g0149others(3): Show | 6 | HG01891.hp1 HG02970.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.828+353G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894211 | ||||||
| chr16:89894216
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.828+358C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894216 | ||||||
| chr16:89894224
|
C | CCCCCGGA others(14): Show |
1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.828+382_828+402dup others(21): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 89894224 | |||||
| chr16:89894255
|
G | GC | 8 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0143others(5): Show | 8 | HG00597.hp1 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.828+402dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 89894255 | |||||
| chr16:89894298
|
G | A | 16 | a0001c0001t0001g0098a0001c0004t0002g0058a0001c0004t0002g0059others(13): Show | 16 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.828+440G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894298 | ||||||
| chr16:89894358
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.828+500G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894358 | ||||||
| chr16:89894363
|
G | GGACGGCC others(14): Show |
16 | a0001c0001t0001g0098a0001c0001t0001g0291a0001c0004t0002g0058others(13): Show | 16 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.828+509_828+529dup others(21): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 89894363 | |||||
| chr16:89894388
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(41): Show | 45 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.828+530A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894388 | ||||||
| chr16:89894406
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(113): Show | 118 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.828+548A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894406 | ||||||
| chr16:89894417
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.828+559G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894417 | ||||||
| chr16:89894732
|
C | A | 58 | a0001c0001t0001g0245a0001c0001t0001g0265a0001c0001t0001g0270others(55): Show | 59 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.829-306C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894732 | ||||||
| chr16:89894737
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-301C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894737 | ||||||
| chr16:89894882
|
T | G | 4 | a0002c0003t0001g0191a0002c0003t0001g0274a0002c0003t0001g0277others(1): Show | 4 | HG03688.hp1 HG04115.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.829-156T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894882 | ||||||
| chr16:89894944
|
C | G | 6 | a0002c0003t0001g0285a0002c0003t0001g0286a0002c0003t0001g0287others(3): Show | 6 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.829-94C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894944 | ||||||
| chr16:89894948
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG00099.hp2 HG01109.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.829-90G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 7/17 | chr16 | 89894948 | ||||||
| chr16:89895185
|
A | G | 57 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(54): Show | 58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.928+48A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895185 | ||||||
| chr16:89895189
|
T | C | 57 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(54): Show | 58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.928+52T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895189 | ||||||
| chr16:89895204
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.928+67G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895204 | ||||||
| chr16:89895239
|
A | G | 20 | a0001c0001t0001g0062a0001c0001t0001g0098a0001c0004t0002g0058others(17): Show | 20 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.928+102A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895239 | ||||||
| chr16:89895253
|
G | A | 57 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(54): Show | 58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.928+116G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895253 | ||||||
| chr16:89895292
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.928+155G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895292 | ||||||
| chr16:89895315
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.928+178A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895315 | ||||||
| chr16:89895355
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.928+218C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895355 | ||||||
| chr16:89895486
|
A | G | 1 | a0001c0004t0002g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.928+349A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895486 | ||||||
| chr16:89895529
|
G | T | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.928+392G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895529 | ||||||
| chr16:89895542
|
A | G | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.928+405A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895542 | ||||||
| chr16:89895549
|
C | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(77): Show | 81 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.928+412C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895549 | ||||||
| chr16:89895629
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.929-361C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895629 | ||||||
| chr16:89895948
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.929-42G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895948 | ||||||
| chr16:89895986
|
A | G | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(98): Show |
splice_region_variant&intron_variant | LOW | c.929-4A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 8/17 | chr16 | 89895986 | ||||||
| chr16:89896227
|
C | A | 36 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(33): Show | 36 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1022+144C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896227 | ||||||
| chr16:89896312
|
G | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1022+229G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896312 | ||||||
| chr16:89896524
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(5): Show | 8 | HG01192.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022+441T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896524 | ||||||
| chr16:89896548
|
CA | C | 7 | a0001c0001t0001g0098a0002c0003t0001g0285a0002c0003t0001g0286others(4): Show | 7 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1022+466delA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896548 | ||||||
| chr16:89896549
|
A | AT | 56 | a0001c0001t0001g0002a0001c0001t0001g0082a0001c0001t0001g0085others(53): Show | 56 | HG00642.hp1 HG00642.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1022+488dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89896549 | |||||
| chr16:89896549
|
A | T | 1 | a0002c0006t0002g0182 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1022+466A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896549 | ||||||
| chr16:89896549
|
AT | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 37 | HG01109.hp1 HG01167.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.1022+488delT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89896549 | |||||
| chr16:89896549
|
ATT | A | 29 | a0001c0001t0001g0291a0001c0002t0001g0021a0001c0002t0001g0022others(26): Show | 29 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.1022+487_1022+488d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89896549 | |||||
| chr16:89896549
|
ATTT | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022+486_1022+488d others(5): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89896549 | |||||
| chr16:89896602
|
G | A | 3 | a0001c0001t0001g0187a0002c0003t0001g0052a0002c0003t0001g0053 | 3 | HG01243.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1022+519G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896602 | ||||||
| chr16:89896627
|
C | T | 1 | a0009c0013t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1022+544C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896627 | ||||||
| chr16:89896649
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1022+566G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896649 | ||||||
| chr16:89896755
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 83 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.1022+672T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896755 | ||||||
| chr16:89896833
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1022+750C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896833 | ||||||
| chr16:89896844
|
G | A | 3 | a0001c0001t0001g0291a0002c0003t0001g0052a0002c0003t0001g0053 | 3 | HG02451.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1022+761G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896844 | ||||||
| chr16:89896881
|
C | G | 38 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1022+798C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896881 | ||||||
| chr16:89896882
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(3): Show | 6 | HG02258.hp1 HG02280.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1022+799G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89896882 | ||||||
| chr16:89897039
|
AAAG | A | 8 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0285others(5): Show | 8 | HG00099.hp2 HG00639.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022+972_1022+974d others(5): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89897039 | |||||
| chr16:89897179
|
A | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022+1096A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897179 | ||||||
| chr16:89897284
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1022+1201C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897284 | ||||||
| chr16:89897368
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1023-1189G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897368 | ||||||
| chr16:89897381
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1023-1176T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897381 | ||||||
| chr16:89897427
|
C | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1023-1130C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897427 | ||||||
| chr16:89897428
|
C | T | 5 | a0001c0001t0001g0264a0002c0003t0001g0285a0002c0003t0001g0287others(2): Show | 5 | HG00099.hp2 HG00639.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1023-1129C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897428 | ||||||
| chr16:89897456
|
C | T | 1 | a0002c0003t0001g0286 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1023-1101C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897456 | ||||||
| chr16:89897637
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1023-920C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897637 | ||||||
| chr16:89897753
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1023-804A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897753 | ||||||
| chr16:89897773
|
A | G | 23 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(20): Show | 24 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.1023-784A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897773 | ||||||
| chr16:89897786
|
C | T | 6 | a0001c0004t0002g0061a0001c0004t0002g0064a0001c0004t0002g0067others(3): Show | 6 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1023-771C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897786 | ||||||
| chr16:89897796
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1023-761A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897796 | ||||||
| chr16:89897819
|
CAAGAT | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(31): Show | 35 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1023-735_1023-731d others(7): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89897819 | |||||
| chr16:89897840
|
G | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023-717G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897840 | ||||||
| chr16:89897841
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1023-716C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897841 | ||||||
| chr16:89897901
|
A | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(76): Show | 80 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1023-656A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897901 | ||||||
| chr16:89897955
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1023-602C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897955 | ||||||
| chr16:89897975
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1023-582T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89897975 | ||||||
| chr16:89898046
|
A | G | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 43 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1023-511A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898046 | ||||||
| chr16:89898108
|
C | CA | 27 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0001g0237others(24): Show | 28 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1023-435dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89898108 | |||||
| chr16:89898108
|
CA | C | 7 | a0001c0001t0001g0087a0001c0001t0001g0142a0001c0001t0001g0164others(4): Show | 7 | HG00733.hp2 HG01192.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1023-435delA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89898108 | |||||
| chr16:89898231
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0217 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1023-326G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898231 | ||||||
| chr16:89898321
|
CTGACTGG others(73): Show |
C | 1 | a0002c0003t0001g0274 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1023-203_1023-124d others(82): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89898321 | |||||
| chr16:89898358
|
G | T | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-199G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898358 | ||||||
| chr16:89898361
|
T | C | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-196T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898361 | ||||||
| chr16:89898366
|
T | C | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-191T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898366 | ||||||
| chr16:89898381
|
T | A | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-176T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898381 | ||||||
| chr16:89898383
|
T | G | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-174T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898383 | ||||||
| chr16:89898385
|
T | C | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-172T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898385 | ||||||
| chr16:89898394
|
G | A | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-163G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898394 | ||||||
| chr16:89898395
|
C | CGGTTGCT others(273): Show |
2 | a0001c0001t0001g0272a0001c0005t0004g0271 | 2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1023-160_1023-159i others(282): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89898395 | |||||
| chr16:89898395
|
C | CGGTTGCT others(273): Show |
36 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(33): Show | 36 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1023-160_1023-159i others(282): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89898395 | |||||
| chr16:89898395
|
C | T | 22 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(19): Show | 23 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1023-162C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898395 | ||||||
| chr16:89898401
|
T | C | 60 | a0001c0001t0001g0098a0001c0001t0001g0264a0001c0001t0001g0265others(57): Show | 61 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1023-156T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898401 | ||||||
| chr16:89898404
|
A | G | 60 | a0001c0001t0001g0098a0001c0001t0001g0264a0001c0001t0001g0265others(57): Show | 61 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1023-153A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898404 | ||||||
| chr16:89898406
|
T | C | 60 | a0001c0001t0001g0098a0001c0001t0001g0264a0001c0001t0001g0265others(57): Show | 61 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.1023-151T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898406 | ||||||
| chr16:89898406
|
T | TGGGGCGC others(73): Show |
38 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(35): Show | 38 | HG01109.hp1 HG01192.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.1023-124_1023-123i others(82): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 89898406 | |||||
| chr16:89898484
|
C | G | 1 | a0002c0003t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1023-73C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898484 | ||||||
| chr16:89898526
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1023-31T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898526 | ||||||
| chr16:89898544
|
A | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(35): Show | 39 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1023-13A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 9/17 | chr16 | 89898544 | ||||||
| chr16:89898674
|
C | T | 1 | a0001c0004t0002g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1115+25C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 10/17 | chr16 | 89898674 | ||||||
| chr16:89898951
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1221+79C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89898951 | ||||||
| chr16:89898985
|
G | A | 1 | a0002c0003t0001g0280 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1221+113G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89898985 | ||||||
| chr16:89899086
|
A | AGAATCCT others(5): Show |
1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1221+216_1221+227d others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 89899086 | |||||
| chr16:89899094
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1221+222C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899094 | ||||||
| chr16:89899107
|
A | C | 5 | a0001c0001t0001g0264a0002c0003t0001g0285a0002c0003t0001g0287others(2): Show | 5 | HG00099.hp2 HG00639.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221+235A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899107 | ||||||
| chr16:89899108
|
C | A | 5 | a0001c0001t0001g0264a0002c0003t0001g0285a0002c0003t0001g0287others(2): Show | 5 | HG00099.hp2 HG00639.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221+236C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899108 | ||||||
| chr16:89899179
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG01109.hp1 HG01192.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1221+307G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899179 | ||||||
| chr16:89899232
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1221+360A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899232 | ||||||
| chr16:89899295
|
A | C | 3 | a0001c0004t0002g0059a0001c0004t0002g0071a0001c0004t0002g0263 | 3 | HG02622.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1221+423A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899295 | ||||||
| chr16:89899356
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1221+484G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899356 | ||||||
| chr16:89899363
|
A | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1221+491A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899363 | ||||||
| chr16:89899417
|
G | C | 38 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1221+545G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899417 | ||||||
| chr16:89899434
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 82 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1221+562C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899434 | ||||||
| chr16:89899560
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1221+688C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899560 | ||||||
| chr16:89899580
|
T | G | 38 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1221+708T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899580 | ||||||
| chr16:89899728
|
C | CA | 27 | a0001c0001t0001g0098a0001c0001t0001g0151a0001c0001t0001g0203others(24): Show | 28 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1221+869dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 89899728 | |||||
| chr16:89899860
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1222-775C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899860 | ||||||
| chr16:89899949
|
T | A | 38 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1222-686T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89899949 | ||||||
| chr16:89900066
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0189 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1222-569G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900066 | ||||||
| chr16:89900197
|
C | CTG | 83 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 84 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1222-437_1222-436d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 89900197 | |||||
| chr16:89900227
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1222-408G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900227 | ||||||
| chr16:89900254
|
C | T | 1 | a0002c0003t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1222-381C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900254 | ||||||
| chr16:89900256
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1222-379C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900256 | ||||||
| chr16:89900260
|
A | G | 38 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1222-375A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900260 | ||||||
| chr16:89900288
|
G | GGGTGGGC others(20): Show |
38 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1222-335_1222-334i others(29): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 89900288 | |||||
| chr16:89900388
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1222-247G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900388 | ||||||
| chr16:89900421
|
C | T | 3 | a0001c0001t0001g0291a0002c0003t0001g0052a0002c0003t0001g0053 | 3 | HG02451.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1222-214C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900421 | ||||||
| chr16:89900433
|
C | G | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1222-202C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900433 | ||||||
| chr16:89900471
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1222-164C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900471 | ||||||
| chr16:89900513
|
C | A | 38 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(35): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1222-122C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900513 | ||||||
| chr16:89900624
|
G | A | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1222-11G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 11/17 | chr16 | 89900624 | ||||||
| chr16:89900809
|
T | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 78 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1381+15T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900809 | ||||||
| chr16:89900815
|
G | A | 4 | a0002c0003t0001g0191a0002c0003t0001g0274a0002c0003t0001g0277others(1): Show | 4 | HG03688.hp1 HG04115.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1381+21G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900815 | ||||||
| chr16:89900843
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1381+49C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900843 | ||||||
| chr16:89900848
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 11 | HG01192.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1381+54G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900848 | ||||||
| chr16:89900865
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1381+71G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900865 | ||||||
| chr16:89900900
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 40 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1381+106T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900900 | ||||||
| chr16:89900937
|
C | T | 7 | a0001c0001t0001g0200a0001c0001t0001g0229a0001c0001t0001g0237others(4): Show | 7 | HG00673.hp1 HG01261.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381+143C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900937 | ||||||
| chr16:89900989
|
A | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 78 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1381+195A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900989 | ||||||
| chr16:89900998
|
C | T | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1381+204C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89900998 | ||||||
| chr16:89901026
|
G | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 40 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1381+232G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901026 | ||||||
| chr16:89901106
|
G | A | 1 | a0001c0005t0004g0271 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1381+312G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901106 | ||||||
| chr16:89901241
|
A | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1381+447A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901241 | ||||||
| chr16:89901262
|
G | A | 1 | a0001c0005t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1381+468G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901262 | ||||||
| chr16:89901273
|
G | A | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0001g0272others(5): Show | 8 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381+479G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901273 | ||||||
| chr16:89901322
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1381+528G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901322 | ||||||
| chr16:89901351
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 40 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1381+557T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901351 | ||||||
| chr16:89901362
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1381+568C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901362 | ||||||
| chr16:89901367
|
AGCTGTGA others(517): Show |
A | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1381+611_1381+1134 others(3): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901367 | |||||
| chr16:89901367
|
AGCTGTGA others(885): Show |
A | 6 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0175others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1381+611_1381+1502 others(3): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901367 | |||||
| chr16:89901414
|
TGAGGGGC others(465): Show |
T | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(81): Show | 85 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1381+1292_1382-156 others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901414 | |||||
| chr16:89901414
|
TGAGGGGC others(1304): Show |
T | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1381+670_1382-1344 others(3): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901414 | |||||
| chr16:89901445
|
C | G | 20 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(17): Show | 21 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1381+651C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901445 | ||||||
| chr16:89901465
|
GCCGGGCG others(466): Show |
G | 1 | a0001c0004t0002g0064 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1381+673_1381+1145 others(3): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901465 | |||||
| chr16:89901474
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1381+680G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901474 | ||||||
| chr16:89901541
|
C | T | 3 | a0001c0004t0002g0068a0001c0004t0002g0069a0001c0004t0002g0071 | 3 | HG02055.hp1 HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1381+747C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901541 | ||||||
| chr16:89901554
|
A | G | 5 | a0001c0001t0001g0098a0002c0003t0001g0275a0002c0003t0001g0281others(2): Show | 5 | HG02886.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381+760A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901554 | ||||||
| chr16:89901561
|
C | T | 5 | a0001c0001t0001g0098a0002c0003t0001g0275a0002c0003t0001g0281others(2): Show | 5 | HG02886.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381+767C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901561 | ||||||
| chr16:89901571
|
A | C | 5 | a0001c0001t0001g0098a0002c0003t0001g0275a0002c0003t0001g0281others(2): Show | 5 | HG02886.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381+777A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901571 | ||||||
| chr16:89901614
|
G | C | 1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1381+820G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901614 | ||||||
| chr16:89901660
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1381+866G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901660 | ||||||
| chr16:89901700
|
G | A | 20 | a0001c0001t0001g0098a0001c0001t0001g0264a0002c0003t0001g0005others(17): Show | 21 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1381+906G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901700 | ||||||
| chr16:89901739
|
C | G | 1 | a0001c0001t0001g0226 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1381+945C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901739 | ||||||
| chr16:89901739
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1381+945C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901739 | ||||||
| chr16:89901754
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1381+960G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901754 | ||||||
| chr16:89901755
|
AAAAAAAA others(464): Show |
A | 3 | a0001c0001t0001g0017a0001c0004t0002g0068a0001c0004t0002g0071 | 3 | HG02055.hp1 HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1381+975_1381+1445 others(3): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901755 | |||||
| chr16:89901755
|
AAAAAAAA others(936): Show |
A | 1 | a0001c0004t0002g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1381+1048_1382-133 others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901755 | |||||
| chr16:89901823
|
CGGGCCTC others(45): Show |
C | 3 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0214 | 3 | NA18970.hp1 NA18993.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1381+1081_1381+113 others(56): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901823 | |||||
| chr16:89901875
|
TGGGCCTC others(832): Show |
T | 1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1381+1142_1382-134 others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901875 | |||||
| chr16:89901886
|
C | CGAGGGGC others(45): Show |
10 | a0001c0001t0001g0264a0002c0003t0001g0276a0002c0003t0001g0278others(7): Show | 10 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1381+1134_1381+113 others(56): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901886 | |||||
| chr16:89901917
|
C | G | 1 | a0002c0003t0001g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1381+1123C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901917 | ||||||
| chr16:89901922
|
TAAGACGG others(309): Show |
T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1381+1142_1381+145 others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901922 | |||||
| chr16:89901927
|
CGGGCCTC others(413): Show |
C | 10 | a0001c0001t0001g0098a0002c0003t0001g0005a0002c0003t0001g0274others(7): Show | 11 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1381+1142_1381+156 others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89901927 | |||||
| chr16:89901945
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1381+1151C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901945 | ||||||
| chr16:89901946
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1381+1152G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901946 | ||||||
| chr16:89901953
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1381+1159C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89901953 | ||||||
| chr16:89902013
|
C | G | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1381+1219C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902013 | ||||||
| chr16:89902013
|
C | T | 13 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0061others(10): Show | 13 | HG02451.hp1 HG02622.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381+1219C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902013 | ||||||
| chr16:89902061
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1381+1267C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902061 | ||||||
| chr16:89902086
|
G | C | 8 | a0001c0001t0001g0051a0001c0001t0001g0265a0001c0001t0001g0270others(5): Show | 8 | HG01109.hp1 HG03239.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.1381+1292G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902086 | ||||||
| chr16:89902086
|
GGGCACCT others(465): Show |
G | 2 | a0001c0001t0001g0188a0001c0001t0001g0205 | 2 | HG02622.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1381+1409_1382-144 others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89902086 | |||||
| chr16:89902172
|
G | A | 11 | a0001c0001t0001g0264a0002c0003t0001g0191a0002c0003t0001g0276others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1381+1378G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902172 | ||||||
| chr16:89902198
|
C | G | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1381+1404C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902198 | ||||||
| chr16:89902203
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0241 | 2 | HG02015.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1381+1409T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902203 | ||||||
| chr16:89902226
|
G | GA | 7 | a0001c0001t0001g0136a0001c0001t0001g0155a0001c0001t0001g0183others(4): Show | 7 | HG01433.hp1 HG02273.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1381+1446dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89902226 | |||||
| chr16:89902227
|
AAAAAAAA others(464): Show |
A | 2 | a0001c0001t0001g0169a0001c0001t0001g0231 | 2 | HG01106.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1381+1520_1382-133 others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89902227 | |||||
| chr16:89902238
|
AAAGACGG others(45): Show |
A | 1 | a0001c0001t0001g0209 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1381+1501_1381+155 others(56): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89902238 | |||||
| chr16:89902244
|
G | C | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1381+1450G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902244 | ||||||
| chr16:89902295
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381+1501C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902295 | ||||||
| chr16:89902296
|
G | A | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1381+1502G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902296 | ||||||
| chr16:89902307
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0083 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1381+1513G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902307 | ||||||
| chr16:89902347
|
T | C | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(19): Show | 22 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1381+1553T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902347 | ||||||
| chr16:89902349
|
G | A | 32 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(29): Show | 33 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.1381+1555G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902349 | ||||||
| chr16:89902358
|
C | CGAGGGGC others(45): Show |
5 | a0002c0003t0001g0276a0002c0003t0001g0278a0002c0003t0001g0279others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381+1606_1381+160 others(56): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89902358 | |||||
| chr16:89902358
|
C | CGAGGGGC others(569): Show |
5 | a0001c0001t0001g0264a0002c0003t0001g0285a0002c0003t0001g0287others(2): Show | 5 | HG00099.hp2 HG00639.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1381+1606_1381+160 others(580): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89902358 | |||||
| chr16:89902358
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(29): Show | 33 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.1381+1564C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902358 | ||||||
| chr16:89902387
|
C | CCCTCCTT others(8): Show |
1 | a0001c0001t0001g0255 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1381+1599_1381+161 others(19): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89902387 | |||||
| chr16:89902416
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1381+1622G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902416 | ||||||
| chr16:89902439
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(17): Show | 20 | HG01109.hp1 HG01192.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1381+1645T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902439 | ||||||
| chr16:89902540
|
T | A | 6 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(3): Show | 6 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1382-1578T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902540 | ||||||
| chr16:89902543
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1382-1575G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902543 | ||||||
| chr16:89902545
|
C | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1382-1573C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902545 | ||||||
| chr16:89902552
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1382-1566G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902552 | ||||||
| chr16:89902553
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1382-1565T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902553 | ||||||
| chr16:89902581
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1382-1537T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902581 | ||||||
| chr16:89902597
|
G | A | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1382-1521G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902597 | ||||||
| chr16:89902648
|
C | T | 2 | a0001c0001t0001g0291a0006c0009t0002g0072 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1382-1470C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902648 | ||||||
| chr16:89902675
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1382-1443C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902675 | ||||||
| chr16:89902676
|
G | A | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1382-1442G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902676 | ||||||
| chr16:89902742
|
T | G | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1382-1376T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902742 | ||||||
| chr16:89902785
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1382-1333G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902785 | ||||||
| chr16:89902846
|
C | T | 37 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(34): Show | 37 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1382-1272C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902846 | ||||||
| chr16:89902936
|
G | C | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1382-1182G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902936 | ||||||
| chr16:89902974
|
C | G | 1 | a0001c0002t0001g0029 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1382-1144C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89902974 | ||||||
| chr16:89903018
|
G | T | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382-1100G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903018 | ||||||
| chr16:89903098
|
C | T | 23 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0175others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1382-1020C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903098 | ||||||
| chr16:89903102
|
G | T | 24 | a0001c0001t0001g0098a0001c0001t0001g0264a0001c0001t0001g0272others(21): Show | 25 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1382-1016G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903102 | ||||||
| chr16:89903154
|
G | A | 23 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0175others(20): Show | 23 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1382-964G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903154 | ||||||
| chr16:89903159
|
A | T | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1382-959A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903159 | ||||||
| chr16:89903180
|
T | G | 24 | a0001c0001t0001g0098a0001c0001t0001g0264a0001c0001t0001g0272others(21): Show | 25 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1382-938T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903180 | ||||||
| chr16:89903185
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1382-933T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903185 | ||||||
| chr16:89903195
|
T | C | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1382-923T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903195 | ||||||
| chr16:89903326
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0189 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1382-792A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903326 | ||||||
| chr16:89903336
|
C | T | 1 | a0001c0005t0004g0271 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1382-782C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903336 | ||||||
| chr16:89903569
|
G | T | 1 | a0001c0001t0001g0198 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1382-549G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903569 | ||||||
| chr16:89903621
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1382-497C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903621 | ||||||
| chr16:89903764
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1382-354G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89903764 | ||||||
| chr16:89903814
|
C | CA | 23 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0100others(20): Show | 23 | HG01071.hp1 HG01175.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1382-295dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 89903814 | |||||
| chr16:89904112
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | splice_region_variant&intron_variant | LOW | c.1382-6C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 12/17 | chr16 | 89904112 | ||||||
| chr16:89904214
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1469+9T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904214 | ||||||
| chr16:89904329
|
G | A | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1469+124G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904329 | ||||||
| chr16:89904334
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1469+129C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904334 | ||||||
| chr16:89904338
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1469+133G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904338 | ||||||
| chr16:89904345
|
A | AT | 61 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0175others(58): Show | 61 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1469+143dupT | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr16 | 89904345 | |||||
| chr16:89904378
|
G | C | 1 | a0001c0002t0001g0025 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1469+173G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904378 | ||||||
| chr16:89904472
|
A | T | 1 | a0002c0003t0001g0005 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1469+267A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904472 | ||||||
| chr16:89904610
|
C | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0185 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1470-328C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904610 | ||||||
| chr16:89904679
|
A | AC | 26 | a0001c0001t0001g0098a0001c0001t0001g0113a0001c0001t0001g0146others(23): Show | 27 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1470-256dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr16 | 89904679 | |||||
| chr16:89904908
|
G | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0134a0001c0001t0001g0195others(6): Show | 10 | HG01168.hp2 HG01169.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1470-30G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 13/17 | chr16 | 89904908 | ||||||
| chr16:89905128
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0265a0001c0001t0001g0270others(5): Show | 8 | HG01943.hp2 HG03239.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.1628+32G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905128 | ||||||
| chr16:89905128
|
G | GC | 5 | a0001c0001t0001g0155a0001c0001t0001g0169a0001c0001t0001g0186others(2): Show | 5 | HG01106.hp1 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1628+37dupC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 89905128 | |||||
| chr16:89905181
|
C | G | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1628+85C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905181 | ||||||
| chr16:89905310
|
C | G | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1628+214C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905310 | ||||||
| chr16:89905324
|
C | T | 2 | a0002c0003t0001g0277a0002c0003t0001g0283 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1628+228C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905324 | ||||||
| chr16:89905440
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1628+344G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905440 | ||||||
| chr16:89905470
|
A | AAATCTGG others(39): Show |
1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1628+374_1628+375i others(48): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905470 | ||||||
| chr16:89905501
|
A | T | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1628+405A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905501 | ||||||
| chr16:89905514
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0203a0001c0001t0001g0234 | 3 | HG02735.hp2 HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1628+418C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905514 | ||||||
| chr16:89905595
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0227 | 2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1628+499G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905595 | ||||||
| chr16:89905681
|
C | T | 44 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 45 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1629-513C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905681 | ||||||
| chr16:89905682
|
G | A | 3 | a0001c0004t0002g0059a0001c0004t0002g0071a0001c0004t0002g0263 | 3 | HG02622.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1629-512G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905682 | ||||||
| chr16:89905714
|
C | T | 7 | a0001c0001t0001g0098a0002c0003t0001g0285a0002c0003t0001g0286others(4): Show | 7 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1629-480C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905714 | ||||||
| chr16:89905737
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1629-457G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905737 | ||||||
| chr16:89905757
|
G | C | 3 | a0001c0004t0002g0059a0001c0004t0002g0071a0001c0004t0002g0263 | 3 | HG02622.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1629-437G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905757 | ||||||
| chr16:89905784
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1629-410A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905784 | ||||||
| chr16:89905850
|
G | T | 7 | a0001c0001t0001g0098a0002c0003t0001g0285a0002c0003t0001g0286others(4): Show | 7 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1629-344G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905850 | ||||||
| chr16:89905911
|
C | T | 18 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0061others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1629-283C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905911 | ||||||
| chr16:89905937
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1629-257T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905937 | ||||||
| chr16:89905999
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1629-195C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89905999 | ||||||
| chr16:89906008
|
C | A | 55 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1629-186C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89906008 | ||||||
| chr16:89906116
|
G | T | 1 | a0001c0001t0001g0215 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1629-78G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89906116 | ||||||
| chr16:89906124
|
A | C | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.1629-70A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 14/17 | chr16 | 89906124 | ||||||
| chr16:89906295
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1719+11A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906295 | ||||||
| chr16:89906336
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1719+52G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906336 | ||||||
| chr16:89906358
|
C | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 10 | HG00099.hp1 HG00735.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1719+74C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906358 | ||||||
| chr16:89906387
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1719+103C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906387 | ||||||
| chr16:89906409
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1719+125G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906409 | ||||||
| chr16:89906456
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0203a0001c0001t0001g0234 | 3 | HG02735.hp2 HG03491.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1719+172C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906456 | ||||||
| chr16:89906458
|
G | A | 5 | a0002c0003t0001g0276a0002c0003t0001g0278a0002c0003t0001g0279others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1719+174G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906458 | ||||||
| chr16:89906503
|
G | T | 1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1719+219G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906503 | ||||||
| chr16:89906596
|
G | C | 6 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0137others(3): Show | 6 | HG00280.hp2 HG00423.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1719+312G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906596 | ||||||
| chr16:89906614
|
C | T | 18 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0061others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1719+330C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906614 | ||||||
| chr16:89906663
|
G | A | 56 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0001t0003g0292others(53): Show | 56 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1719+379G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906663 | ||||||
| chr16:89906683
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1719+399G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906683 | ||||||
| chr16:89906719
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1719+435C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906719 | ||||||
| chr16:89906809
|
G | C | 18 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0061others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1720-434G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906809 | ||||||
| chr16:89906860
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1720-383G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906860 | ||||||
| chr16:89906933
|
G | A | 1 | a0001c0004t0002g0065 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1720-310G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906933 | ||||||
| chr16:89906938
|
G | GAAGATGT others(29): Show |
1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1720-304_1720-269d others(38): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 89906938 | |||||
| chr16:89906959
|
C | T | 1 | a0002c0003t0001g0282 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1720-284C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89906959 | ||||||
| chr16:89907001
|
G | T | 1 | a0002c0003t0001g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1720-242G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89907001 | ||||||
| chr16:89907025
|
A | C | 1 | a0001c0005t0004g0271 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1720-218A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89907025 | ||||||
| chr16:89907132
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1720-111C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89907132 | ||||||
| chr16:89907212
|
TAGCATCT others(3): Show |
T | 1 | a0001c0001t0001g0255 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1720-30_1720-21del others(10): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 15/17 | chr16 | 89907212 | ||||||
| chr16:89907343
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1799+21C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907343 | ||||||
| chr16:89907346
|
A | ACCTCCCT others(7): Show |
1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1799+30_1799+31ins others(14): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907346 | |||||
| chr16:89907359
|
C | T | 1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1799+37C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907359 | ||||||
| chr16:89907360
|
A | G | 1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1799+38A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907360 | ||||||
| chr16:89907361
|
C | G | 1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1799+39C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907361 | ||||||
| chr16:89907367
|
T | A | 1 | a0001c0005t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1799+45T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907367 | ||||||
| chr16:89907369
|
CTCCCAGT | C | 5 | a0001c0001t0001g0111a0001c0001t0001g0150a0001c0001t0001g0171others(2): Show | 5 | HG01175.hp2 HG01346.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1799+54_1799+60del others(7): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907369 | |||||
| chr16:89907374
|
A | AGCTCCCG | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1799+53_1799+54ins others(7): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907374 | |||||
| chr16:89907374
|
A | T | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1799+52A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907374 | ||||||
| chr16:89907375
|
G | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1799+53G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907375 | ||||||
| chr16:89907375
|
G | GCTCCCGG others(147): Show |
1 | a0001c0001t0001g0213 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1799+53_1799+54ins others(154): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907375 | ||||||
| chr16:89907376
|
T | C | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1799+54T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907376 | ||||||
| chr16:89907381
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0169 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1799+59A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907381 | ||||||
| chr16:89907382
|
G | A | 3 | a0001c0001t0001g0264a0002c0003t0001g0052a0002c0003t0001g0053 | 3 | HG00099.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1799+60G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907382 | ||||||
| chr16:89907382
|
G | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1799+60G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907382 | ||||||
| chr16:89907387
|
C | T | 54 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(51): Show | 54 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1799+65C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907387 | ||||||
| chr16:89907388
|
A | G | 103 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(100): Show | 104 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1799+66A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907388 | ||||||
| chr16:89907389
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0169 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1799+67G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907389 | ||||||
| chr16:89907390
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1799+68C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907390 | ||||||
| chr16:89907395
|
A | AGTTCCAC others(118): Show |
1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1799+73_1799+74ins others(125): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907395 | ||||||
| chr16:89907395
|
A | AGTTCCCA others(112): Show |
1 | a0001c0001t0001g0169 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1799+73_1799+74ins others(119): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907395 | ||||||
| chr16:89907402
|
A | T | 2 | a0001c0001t0001g0213a0001c0005t0001g0267 | 2 | HG02040.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1799+80A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907402 | ||||||
| chr16:89907403
|
G | C | 2 | a0001c0001t0001g0213a0001c0005t0001g0267 | 2 | HG02040.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1799+81G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907403 | ||||||
| chr16:89907404
|
C | T | 105 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 106 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1799+82C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907404 | ||||||
| chr16:89907408
|
A | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+86A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907408 | ||||||
| chr16:89907409
|
A | T | 2 | a0001c0001t0001g0213a0001c0005t0001g0267 | 2 | HG02040.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1799+87A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907409 | ||||||
| chr16:89907413
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(291): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1799+91T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907413 | ||||||
| chr16:89907416
|
A | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1799+94A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907416 | ||||||
| chr16:89907417
|
G | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1799+95G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907417 | ||||||
| chr16:89907417
|
G | GCTCCCAC others(322): Show |
1 | a0002c0003t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1799+101_1799+102i others(331): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907417 | |||||
| chr16:89907417
|
G | GCTCCCAC others(322): Show |
5 | a0001c0001t0001g0098a0002c0003t0001g0285a0002c0003t0001g0288others(2): Show | 5 | HG00639.hp1 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1799+101_1799+102i others(331): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907417 | |||||
| chr16:89907417
|
G | GCTCCCAC others(336): Show |
9 | a0001c0001t0001g0007a0001c0001t0001g0272a0002c0003t0001g0191others(6): Show | 9 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1799+101_1799+102i others(345): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907417 | |||||
| chr16:89907417
|
G | GCTCCCAC others(337): Show |
1 | a0002c0003t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1799+101_1799+102i others(346): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907417 | |||||
| chr16:89907422
|
C | T | 2 | a0001c0001t0001g0213a0001c0005t0001g0267 | 2 | HG02040.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1799+100C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907422 | ||||||
| chr16:89907423
|
A | ACCTCCCT others(111): Show |
1 | a0002c0003t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1799+101_1799+102i others(120): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907423 | ||||||
| chr16:89907423
|
A | ACCTCCCT others(84): Show |
1 | a0002c0003t0001g0276 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1799+101_1799+102i others(93): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907423 | ||||||
| chr16:89907423
|
A | G | 2 | a0001c0001t0001g0213a0001c0005t0001g0267 | 2 | HG02040.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1799+101A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907423 | ||||||
| chr16:89907424
|
G | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1799+102G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907424 | ||||||
| chr16:89907430
|
A | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1799+108A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907430 | ||||||
| chr16:89907434
|
A | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+112A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907434 | ||||||
| chr16:89907435
|
G | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+113G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907435 | ||||||
| chr16:89907437
|
A | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1799+115A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907437 | ||||||
| chr16:89907438
|
G | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1799+116G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907438 | ||||||
| chr16:89907439
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1799+117C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907439 | ||||||
| chr16:89907444
|
G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 251 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1799+122G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907444 | ||||||
| chr16:89907444
|
G | T | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(44): Show | 48 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1799+122G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907444 | ||||||
| chr16:89907445
|
G | C | 50 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(47): Show | 51 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1799+123G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907445 | ||||||
| chr16:89907450
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1799+128T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907450 | ||||||
| chr16:89907451
|
G | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(34): Show | 37 | HG00639.hp1 HG01109.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.1799+129G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907451 | ||||||
| chr16:89907451
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1799+129G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907451 | ||||||
| chr16:89907452
|
G | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1799+130G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907452 | ||||||
| chr16:89907458
|
A | ACCTCCCA others(28): Show |
6 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(3): Show | 6 | HG03239.hp2 HG03669.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1799+142_1799+143i others(37): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907458 | |||||
| chr16:89907458
|
A | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+136A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907458 | ||||||
| chr16:89907458
|
A | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1799+136A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907458 | ||||||
| chr16:89907458
|
ACCTCCCT | A | 15 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0063others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1799+143_1799+149d others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907458 | |||||
| chr16:89907459
|
C | CCTCCCAG others(84): Show |
1 | a0001c0001t0001g0169 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1799+142_1799+143i others(93): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907459 | |||||
| chr16:89907459
|
C | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1799+137C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907459 | ||||||
| chr16:89907460
|
C | CTCCCAGT others(105): Show |
1 | a0001c0002t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1799+142_1799+143i others(114): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907460 | |||||
| chr16:89907460
|
C | CTCCCAGT others(112): Show |
27 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(24): Show | 27 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1799+142_1799+143i others(121): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907460 | |||||
| chr16:89907460
|
C | CTCCCAGT others(105): Show |
2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1799+142_1799+143i others(114): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907460 | |||||
| chr16:89907462
|
C | CCCAGTTC others(3): Show |
2 | a0001c0004t0002g0061a0006c0009t0002g0072 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+142_1799+143i others(12): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907462 | |||||
| chr16:89907465
|
T | A | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(68): Show | 72 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1799+143T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907465 | ||||||
| chr16:89907466
|
C | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1799+144C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907466 | ||||||
| chr16:89907472
|
A | T | 1 | a0002c0003t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1799+150A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907472 | ||||||
| chr16:89907473
|
C | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1799+151C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907473 | ||||||
| chr16:89907474
|
C | CTCCCAGT | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+157_1799+158i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907474 | |||||
| chr16:89907474
|
C | CTCCCTCC others(21): Show |
1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+156_1799+157i others(30): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907474 | |||||
| chr16:89907474
|
C | T | 38 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0169others(35): Show | 39 | HG00639.hp1 HG01106.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.1799+152C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907474 | ||||||
| chr16:89907476
|
C | CCCACCTC others(73): Show |
1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1799+163_1799+164i others(82): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907476 | |||||
| chr16:89907478
|
C | T | 1 | a0002c0003t0001g0276 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1799+156C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907478 | ||||||
| chr16:89907479
|
A | G | 1 | a0002c0003t0001g0276 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1799+157A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907479 | ||||||
| chr16:89907479
|
A | T | 7 | a0001c0001t0001g0259a0001c0001t0001g0264a0001c0001t0003g0292others(4): Show | 7 | HG00099.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+157A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907479 | ||||||
| chr16:89907480
|
C | G | 2 | a0002c0003t0001g0053a0002c0003t0001g0276 | 2 | HG01167.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1799+158C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907480 | ||||||
| chr16:89907481
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1799+159C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907481 | ||||||
| chr16:89907485
|
C | T | 1 | a0002c0003t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1799+163C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907485 | ||||||
| chr16:89907486
|
A | G | 1 | a0002c0003t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1799+164A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907486 | ||||||
| chr16:89907486
|
A | T | 31 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1799+164A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907486 | ||||||
| chr16:89907487
|
G | C | 35 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(32): Show | 35 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1799+165G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907487 | ||||||
| chr16:89907488
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1799+166C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907488 | ||||||
| chr16:89907493
|
A | T | 3 | a0001c0004t0002g0061a0001c0004t0002g0069a0006c0009t0002g0072 | 3 | HG02055.hp2 HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+171A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907493 | ||||||
| chr16:89907494
|
C | G | 31 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1799+172C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907494 | ||||||
| chr16:89907495
|
C | CTCCCACC others(91): Show |
4 | a0002c0003t0001g0005a0002c0003t0001g0275a0002c0003t0001g0281others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1799+177_1799+178i others(100): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907495 | |||||
| chr16:89907495
|
C | CTCCCAGT others(119): Show |
2 | a0001c0001t0001g0264a0002c0003t0001g0052 | 2 | HG00099.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1799+177_1799+178i others(128): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907495 | |||||
| chr16:89907495
|
C | T | 1 | a0002c0003t0001g0276 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1799+173C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907495 | ||||||
| chr16:89907500
|
T | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1799+178T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907500 | ||||||
| chr16:89907501
|
C | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 196 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1799+179C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907501 | ||||||
| chr16:89907505
|
C | CCTCCTCT | 3 | a0001c0001t0001g0100a0001c0001t0001g0169a0001c0001t0001g0213 | 3 | HG01106.hp1 HG01516.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1799+184_1799+185i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907505 | |||||
| chr16:89907507
|
A | ACCTCCCT | 17 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(14): Show | 17 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1799+191_1799+192i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907507 | |||||
| chr16:89907507
|
A | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(5): Show | 8 | HG02897.hp1 HG03239.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.1799+185A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907507 | ||||||
| chr16:89907508
|
C | G | 45 | a0001c0001t0001g0100a0001c0001t0001g0169a0001c0001t0001g0213others(42): Show | 46 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1799+186C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907508 | ||||||
| chr16:89907514
|
A | AGCTCCTG | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+192_1799+193i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907514 | ||||||
| chr16:89907514
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0169a0001c0001t0001g0213 | 3 | HG01106.hp1 HG01516.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1799+192A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907514 | ||||||
| chr16:89907514
|
A | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 230 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1799+192A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907514 | ||||||
| chr16:89907515
|
C | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0100others(23): Show | 26 | HG00639.hp1 HG01106.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.1799+193C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907515 | ||||||
| chr16:89907521
|
T | A | 11 | a0001c0001t0001g0100a0001c0001t0001g0169a0001c0001t0001g0213others(8): Show | 11 | HG01106.hp1 HG01516.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1799+199T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907521 | ||||||
| chr16:89907521
|
T | TCCTCCCA others(182): Show |
1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1799+206_1799+207i others(191): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907521 | |||||
| chr16:89907521
|
T | TCCTCCCA others(7): Show |
30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+207_1799+208i others(16): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907521 | |||||
| chr16:89907522
|
C | G | 1 | a0001c0004t0002g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1799+200C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907522 | ||||||
| chr16:89907528
|
A | T | 2 | a0001c0004t0002g0061a0006c0009t0002g0072 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+206A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907528 | ||||||
| chr16:89907529
|
G | C | 3 | a0001c0004t0002g0061a0001c0004t0002g0069a0006c0009t0002g0072 | 3 | HG02055.hp2 HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+207G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907529 | ||||||
| chr16:89907530
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1799+208T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907530 | ||||||
| chr16:89907532
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0178 | 2 | NA18949.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1799+210C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907532 | ||||||
| chr16:89907534
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(291): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1799+212T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907534 | ||||||
| chr16:89907535
|
A | T | 1 | a0001c0004t0002g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1799+213A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907535 | ||||||
| chr16:89907536
|
C | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(35): Show | 39 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1799+214C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907536 | ||||||
| chr16:89907541
|
C | T | 2 | a0001c0004t0002g0061a0006c0009t0002g0072 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+219C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907541 | ||||||
| chr16:89907542
|
A | G | 2 | a0001c0004t0002g0061a0006c0009t0002g0072 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+220A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907542 | ||||||
| chr16:89907542
|
A | T | 31 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(28): Show | 31 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1799+220A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907542 | ||||||
| chr16:89907543
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(34): Show | 38 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1799+221T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907543 | ||||||
| chr16:89907543
|
T | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1799+221T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907543 | ||||||
| chr16:89907544
|
C | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0264others(21): Show | 25 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1799+222C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907544 | ||||||
| chr16:89907549
|
A | ACCTCCCT | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+227_1799+228i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907549 | ||||||
| chr16:89907549
|
A | G | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+227A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907549 | ||||||
| chr16:89907550
|
G | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1799+228G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907550 | ||||||
| chr16:89907550
|
G | GCTCCTGG others(7): Show |
1 | a0001c0004t0002g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1799+232_1799+233i others(16): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907550 | |||||
| chr16:89907550
|
G | GTTTCCAC | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+228_1799+229i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907550 | ||||||
| chr16:89907556
|
A | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1799+234A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907556 | ||||||
| chr16:89907557
|
G | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1799+235G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907557 | ||||||
| chr16:89907558
|
C | T | 4 | a0001c0001t0001g0096a0001c0004t0002g0061a0001c0004t0002g0069others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1799+236C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907558 | ||||||
| chr16:89907560
|
G | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(291): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1799+238G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907560 | ||||||
| chr16:89907560
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+238G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907560 | ||||||
| chr16:89907563
|
A | ACCTCCCT others(7): Show |
16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+247_1799+248i others(16): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907563 | |||||
| chr16:89907563
|
A | T | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1799+241A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907563 | ||||||
| chr16:89907564
|
C | G | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+242C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907564 | ||||||
| chr16:89907565
|
C | T | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+243C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907565 | ||||||
| chr16:89907568
|
C | T | 10 | a0001c0001t0001g0213a0001c0001t0001g0264a0001c0001t0003g0292others(7): Show | 11 | HG00099.hp2 HG01167.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1799+246C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907568 | ||||||
| chr16:89907570
|
A | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+248A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907570 | ||||||
| chr16:89907571
|
G | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1799+249G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907571 | ||||||
| chr16:89907574
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+252T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907574 | ||||||
| chr16:89907576
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+254T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907576 | ||||||
| chr16:89907576
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0057others(101): Show | 106 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1799+254T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907576 | ||||||
| chr16:89907576
|
T | TGGCTCCC others(140): Show |
1 | a0002c0003t0001g0286 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1799+255_1799+256i others(149): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907576 | |||||
| chr16:89907577
|
G | A | 41 | a0001c0001t0001g0096a0001c0001t0001g0265a0001c0001t0001g0270others(38): Show | 41 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.1799+255G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907577 | ||||||
| chr16:89907577
|
G | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+255G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907577 | ||||||
| chr16:89907578
|
C | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1799+256C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907578 | ||||||
| chr16:89907581
|
C | T | 2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1799+259C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907581 | ||||||
| chr16:89907584
|
T | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1799+262T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907584 | ||||||
| chr16:89907585
|
C | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+263C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907585 | ||||||
| chr16:89907590
|
C | T | 1 | a0001c0004t0002g0059 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1799+268C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907590 | ||||||
| chr16:89907591
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1799+269A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907591 | ||||||
| chr16:89907593
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(73): Show | 77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1799+271T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907593 | ||||||
| chr16:89907595
|
C | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+273C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907595 | ||||||
| chr16:89907598
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+276A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907598 | ||||||
| chr16:89907607
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(70): Show | 74 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1799+285C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907607 | ||||||
| chr16:89907609
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+287C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907609 | ||||||
| chr16:89907612
|
A | ACCTCCCT others(91): Show |
15 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0063others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1799+296_1799+297i others(100): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(182): Show |
16 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1799+296_1799+297i others(191): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(167): Show |
1 | a0001c0001t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1799+296_1799+297i others(176): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(161): Show |
1 | a0001c0001t0001g0157 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1799+296_1799+297i others(170): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(168): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0178 | 2 | NA18949.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1799+296_1799+297i others(177): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(168): Show |
141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 143 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1799+296_1799+297i others(177): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(168): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0202 | 2 | HG02257.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1799+296_1799+297i others(177): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(168): Show |
6 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0175others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1799+296_1799+297i others(177): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(169): Show |
1 | a0001c0001t0001g0233 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1799+296_1799+297i others(178): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | ACCTCCCT others(7): Show |
3 | a0001c0001t0001g0213a0001c0001t0003g0292a0002c0003t0001g0286 | 3 | HG02040.hp2 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1799+296_1799+297i others(16): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907612 | |||||
| chr16:89907612
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+290A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907612 | ||||||
| chr16:89907613
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+291C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907613 | ||||||
| chr16:89907617
|
C | CCTCCTCC others(104): Show |
1 | a0007c0008t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1799+296_1799+297i others(113): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907617 | |||||
| chr16:89907617
|
C | CCTCCTCC others(7): Show |
8 | a0001c0001t0001g0264a0002c0003t0001g0005a0002c0003t0001g0052others(5): Show | 9 | HG00099.hp2 HG01167.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1799+296_1799+297i others(16): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907617 | |||||
| chr16:89907619
|
A | T | 31 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0098others(28): Show | 31 | HG00639.hp1 HG01106.hp1 HG01516.hp1 others(28): Show |
intron_variant | MODIFIER | c.1799+297A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907619 | ||||||
| chr16:89907620
|
G | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0098others(21): Show | 24 | HG00639.hp1 HG01106.hp1 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.1799+298G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907620 | ||||||
| chr16:89907620
|
G | T | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+298G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907620 | ||||||
| chr16:89907625
|
C | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+303C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907625 | ||||||
| chr16:89907625
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1799+303C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907625 | ||||||
| chr16:89907626
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0057others(72): Show | 76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1799+304G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907626 | ||||||
| chr16:89907626
|
G | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+304G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907626 | ||||||
| chr16:89907627
|
C | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 213 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1799+305C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907627 | ||||||
| chr16:89907628
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1799+306C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907628 | ||||||
| chr16:89907633
|
T | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1799+311T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907633 | ||||||
| chr16:89907633
|
T | TCCTCCCT others(28): Show |
1 | a0001c0001t0001g0169 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1799+312_1799+313i others(37): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907633 | |||||
| chr16:89907634
|
C | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+312C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907634 | ||||||
| chr16:89907635
|
A | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+313A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907635 | ||||||
| chr16:89907639
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+317T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907639 | ||||||
| chr16:89907640
|
A | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+318A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907640 | ||||||
| chr16:89907640
|
A | T | 37 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(34): Show | 38 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1799+318A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907640 | ||||||
| chr16:89907641
|
G | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(64): Show | 68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1799+319G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907641 | ||||||
| chr16:89907642
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0057others(81): Show | 85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1799+320T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907642 | ||||||
| chr16:89907643
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+321T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907643 | ||||||
| chr16:89907644
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+322C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907644 | ||||||
| chr16:89907647
|
A | T | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+325A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907647 | ||||||
| chr16:89907648
|
C | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(34): Show | 38 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1799+326C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907648 | ||||||
| chr16:89907649
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+327C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907649 | ||||||
| chr16:89907651
|
C | CCCTCCTC others(161): Show |
1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1799+331_1799+332i others(170): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907651 | |||||
| chr16:89907652
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+330C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907652 | ||||||
| chr16:89907654
|
A | T | 33 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0291others(30): Show | 33 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1799+332A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907654 | ||||||
| chr16:89907655
|
G | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(66): Show | 70 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1799+333G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907655 | ||||||
| chr16:89907655
|
G | GTTTCCAC | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+333_1799+334i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907655 | ||||||
| chr16:89907656
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1799+334C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907656 | ||||||
| chr16:89907661
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+339A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907661 | ||||||
| chr16:89907662
|
G | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 212 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1799+340G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907662 | ||||||
| chr16:89907667
|
C | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+345C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907667 | ||||||
| chr16:89907668
|
T | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0057others(50): Show | 54 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1799+346T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907668 | ||||||
| chr16:89907668
|
T | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+346T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907668 | ||||||
| chr16:89907669
|
C | CCTCCCAG others(196): Show |
30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+353_1799+354i others(205): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907669 | |||||
| chr16:89907669
|
C | CCTCCCTC others(42): Show |
1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1799+352_1799+353i others(51): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907669 | |||||
| chr16:89907669
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0291 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1799+347C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907669 | ||||||
| chr16:89907674
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+352C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907674 | ||||||
| chr16:89907675
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+353A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907675 | ||||||
| chr16:89907675
|
A | T | 20 | a0001c0001t0001g0169a0001c0001t0001g0264a0001c0001t0001g0265others(17): Show | 21 | HG00099.hp2 HG01106.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1799+353A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907675 | ||||||
| chr16:89907676
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0100 | 2 | HG01516.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1799+354C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907676 | ||||||
| chr16:89907682
|
A | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 191 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1799+360A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907682 | ||||||
| chr16:89907683
|
C | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+361C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907683 | ||||||
| chr16:89907683
|
C | CCTCCCAG | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+366_1799+367i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907683 | |||||
| chr16:89907683
|
C | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0057others(55): Show | 60 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.1799+361C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907683 | ||||||
| chr16:89907685
|
T | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1799+363T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907685 | ||||||
| chr16:89907686
|
C | CCCAGCTC others(3): Show |
1 | a0001c0001t0001g0169 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1799+366_1799+367i others(12): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907686 | |||||
| chr16:89907689
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1799+367T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907689 | ||||||
| chr16:89907689
|
T | G | 18 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0270others(15): Show | 19 | HG00099.hp2 HG01167.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1799+367T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907689 | ||||||
| chr16:89907690
|
C | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(34): Show | 38 | HG00099.hp2 HG01167.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.1799+368C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907690 | ||||||
| chr16:89907691
|
C | CTCCCAGC others(84): Show |
15 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0063others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1799+370_1799+371i others(93): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907691 | |||||
| chr16:89907691
|
C | CTCCCAGC others(91): Show |
1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1799+370_1799+371i others(100): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907691 | |||||
| chr16:89907691
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1799+369C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907691 | ||||||
| chr16:89907691
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0100 | 2 | HG01516.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1799+369C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907691 | ||||||
| chr16:89907693
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1799+371T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907693 | ||||||
| chr16:89907694
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1799+372T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907694 | ||||||
| chr16:89907696
|
A | AGCTCCCT | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 150 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1799+374_1799+375i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907696 | ||||||
| chr16:89907696
|
A | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(83): Show | 87 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1799+374A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907696 | ||||||
| chr16:89907697
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0126others(4): Show | 7 | HG00423.hp1 HG01109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+375C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907697 | ||||||
| chr16:89907698
|
C | CTCCCAGT | 3 | a0001c0004t0002g0061a0001c0004t0002g0069a0006c0009t0002g0072 | 3 | HG02055.hp2 HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+381_1799+382i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907698 | |||||
| chr16:89907699
|
T | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+377T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907699 | ||||||
| chr16:89907703
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1799+381A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907703 | ||||||
| chr16:89907703
|
A | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(69): Show | 73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1799+381A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907703 | ||||||
| chr16:89907704
|
C | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1799+382C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907704 | ||||||
| chr16:89907705
|
C | T | 15 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0270others(12): Show | 16 | HG00099.hp2 HG01167.hp1 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+383C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907705 | ||||||
| chr16:89907707
|
G | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(291): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1799+385G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907707 | ||||||
| chr16:89907708
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+386C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907708 | ||||||
| chr16:89907709
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+387C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907709 | ||||||
| chr16:89907710
|
A | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 153 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1799+388A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907710 | ||||||
| chr16:89907711
|
C | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0051a0001c0001t0001g0057others(73): Show | 77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1799+389C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907711 | ||||||
| chr16:89907712
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1799+390C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907712 | ||||||
| chr16:89907714
|
C | CCCAGTTC others(63): Show |
16 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+394_1799+395i others(72): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907714 | |||||
| chr16:89907716
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1799+394C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907716 | ||||||
| chr16:89907717
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 206 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1799+395G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907717 | ||||||
| chr16:89907717
|
G | T | 25 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0126others(22): Show | 25 | HG00423.hp1 HG01106.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.1799+395G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907717 | ||||||
| chr16:89907718
|
C | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1799+396C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907718 | ||||||
| chr16:89907719
|
C | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0098others(14): Show | 17 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1799+397C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907719 | ||||||
| chr16:89907721
|
C | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+399C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907721 | ||||||
| chr16:89907724
|
A | T | 22 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0169others(19): Show | 22 | HG01106.hp1 HG01516.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1799+402A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907724 | ||||||
| chr16:89907725
|
C | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 21 | HG00423.hp1 HG01109.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1799+403C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907725 | ||||||
| chr16:89907728
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(291): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.1799+406T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907728 | ||||||
| chr16:89907731
|
A | T | 16 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0270others(13): Show | 17 | HG00099.hp2 HG01167.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.1799+409A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907731 | ||||||
| chr16:89907732
|
G | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 41 | HG00099.hp2 HG00423.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1799+410G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907732 | ||||||
| chr16:89907733
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1799+411C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907733 | ||||||
| chr16:89907735
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1799+413C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907735 | ||||||
| chr16:89907737
|
C | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+415C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907737 | ||||||
| chr16:89907738
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1799+416G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907738 | ||||||
| chr16:89907738
|
G | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 21 | HG01109.hp1 HG01192.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1799+416G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907738 | ||||||
| chr16:89907739
|
C | G | 22 | a0001c0001t0001g0100a0001c0001t0001g0126a0001c0001t0001g0169others(19): Show | 22 | HG00423.hp1 HG01106.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.1799+417C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907739 | ||||||
| chr16:89907740
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0001g0173a0001c0001t0001g0175others(1): Show | 4 | HG00423.hp1 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1799+418C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907740 | ||||||
| chr16:89907741
|
T | G | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1799+419T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907741 | ||||||
| chr16:89907745
|
A | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 53 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.1799+423A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907745 | ||||||
| chr16:89907746
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1799+424C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907746 | ||||||
| chr16:89907749
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+427T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907749 | ||||||
| chr16:89907751
|
C | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(63): Show | 67 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1799+429C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907751 | ||||||
| chr16:89907752
|
A | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(14): Show | 17 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1799+430A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907752 | ||||||
| chr16:89907753
|
G | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1799+431G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907753 | ||||||
| chr16:89907753
|
G | GTTTCCAC others(140): Show |
2 | a0001c0001t0001g0169a0001c0001t0003g0292 | 2 | HG01106.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1799+431_1799+432i others(149): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907753 | ||||||
| chr16:89907753
|
G | GTTTCCAC others(140): Show |
15 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0063others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1799+431_1799+432i others(149): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907753 | ||||||
| chr16:89907753
|
G | GTTTCCAC others(198): Show |
1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1799+431_1799+432i others(207): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907753 | ||||||
| chr16:89907756
|
C | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+434C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907756 | ||||||
| chr16:89907759
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0098others(19): Show | 22 | HG00423.hp1 HG00639.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1799+437G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907759 | ||||||
| chr16:89907759
|
G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1799+437G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907759 | ||||||
| chr16:89907760
|
C | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(33): Show | 36 | HG00639.hp1 HG01109.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.1799+438C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907760 | ||||||
| chr16:89907761
|
C | T | 16 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(13): Show | 16 | HG00639.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1799+439C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907761 | ||||||
| chr16:89907766
|
T | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 54 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1799+444T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907766 | ||||||
| chr16:89907767
|
C | G | 17 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0270others(14): Show | 18 | HG00099.hp2 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1799+445C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907767 | ||||||
| chr16:89907770
|
C | CCCTCCTC others(245): Show |
2 | a0001c0001t0001g0173a0001c0001t0001g0175 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1799+450_1799+451i others(254): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907770 | |||||
| chr16:89907770
|
C | CCCTCCTC others(224): Show |
1 | a0001c0001t0001g0126 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1799+450_1799+451i others(233): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907770 | |||||
| chr16:89907770
|
C | CCCTCCTC others(253): Show |
1 | a0001c0001t0001g0217 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1799+450_1799+451i others(262): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907770 | |||||
| chr16:89907770
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(81): Show | 85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1799+448C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907770 | ||||||
| chr16:89907771
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+449C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907771 | ||||||
| chr16:89907773
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+451A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907773 | ||||||
| chr16:89907774
|
G | C | 18 | a0001c0001t0001g0096a0001c0001t0001g0264a0001c0001t0001g0265others(15): Show | 19 | HG00099.hp2 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1799+452G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907774 | ||||||
| chr16:89907775
|
T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1799+453T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907775 | ||||||
| chr16:89907777
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+455C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907777 | ||||||
| chr16:89907780
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+458A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907780 | ||||||
| chr16:89907780
|
A | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+458A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907780 | ||||||
| chr16:89907781
|
C | CCTCCCAG | 4 | a0001c0001t0001g0126a0001c0001t0001g0173a0001c0001t0001g0175others(1): Show | 4 | HG00423.hp1 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1799+465_1799+466i others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907781 | |||||
| chr16:89907781
|
C | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1799+459C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907781 | ||||||
| chr16:89907782
|
C | T | 17 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0270others(14): Show | 18 | HG00099.hp2 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1799+460C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907782 | ||||||
| chr16:89907784
|
C | CCCAGCTC others(49): Show |
1 | a0002c0003t0001g0276 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1799+465_1799+466i others(58): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907784 | |||||
| chr16:89907788
|
C | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(99): Show | 103 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1799+466C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907788 | ||||||
| chr16:89907793
|
C | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+471C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907793 | ||||||
| chr16:89907794
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+472A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907794 | ||||||
| chr16:89907795
|
G | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(98): Show | 102 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1799+473G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907795 | ||||||
| chr16:89907796
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 154 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.1799+474C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907796 | ||||||
| chr16:89907798
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 153 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1799+476C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907798 | ||||||
| chr16:89907801
|
A | T | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1799+479A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907801 | ||||||
| chr16:89907802
|
C | G | 38 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(35): Show | 39 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1799+480C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907802 | ||||||
| chr16:89907806
|
C | T | 21 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0126others(18): Show | 21 | HG00423.hp1 HG00639.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1799+484C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907806 | ||||||
| chr16:89907808
|
A | T | 41 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0126others(38): Show | 42 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1799+486A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907808 | ||||||
| chr16:89907809
|
A | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0018others(77): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1799+487A>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907809 | ||||||
| chr16:89907809
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1799+487A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907809 | ||||||
| chr16:89907810
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+488C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907810 | ||||||
| chr16:89907812
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+490C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907812 | ||||||
| chr16:89907813
|
C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(35): Show | 39 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1799+491C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907813 | ||||||
| chr16:89907815
|
T | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 205 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1799+493T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907815 | ||||||
| chr16:89907816
|
C | G | 4 | a0002c0003t0001g0005a0002c0003t0001g0275a0002c0003t0001g0281others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1799+494C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907816 | ||||||
| chr16:89907819
|
C | CCCAGCTC others(21): Show |
21 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0126others(18): Show | 21 | HG00423.hp1 HG00639.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1799+500_1799+501i others(30): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907819 | |||||
| chr16:89907819
|
C | CCCAGCTC others(217): Show |
1 | a0002c0003t0001g0276 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1799+500_1799+501i others(226): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907819 | |||||
| chr16:89907819
|
C | CCCAGCTC others(266): Show |
1 | a0001c0001t0001g0207 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1799+500_1799+501i others(275): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907819 | |||||
| chr16:89907819
|
C | CCCAGCTC others(280): Show |
3 | a0001c0001t0001g0264a0002c0003t0001g0052a0002c0003t0001g0053 | 3 | HG00099.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1799+500_1799+501i others(289): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907819 | |||||
| chr16:89907819
|
C | CCCAGCTC others(336): Show |
7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+500_1799+501i others(345): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907819 | |||||
| chr16:89907819
|
C | CCTCCCTC others(268): Show |
1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1799+498_1799+499i others(277): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907819 | |||||
| chr16:89907819
|
C | CTCTCCTC others(35): Show |
45 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(42): Show | 45 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1799+497_1799+498i others(44): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907819 | ||||||
| chr16:89907822
|
A | G | 4 | a0002c0003t0001g0005a0002c0003t0001g0275a0002c0003t0001g0281others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1799+500A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907822 | ||||||
| chr16:89907822
|
A | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1799+500A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907822 | ||||||
| chr16:89907823
|
C | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0096a0001c0004t0002g0061others(7): Show | 11 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1799+501C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907823 | ||||||
| chr16:89907825
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+503T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907825 | ||||||
| chr16:89907829
|
A | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 150 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1799+507A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907829 | ||||||
| chr16:89907830
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0057others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799+508C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907830 | ||||||
| chr16:89907832
|
T | TCCCAGCT others(279): Show |
1 | a0001c0001t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1799+511_1799+512i others(288): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907832 | |||||
| chr16:89907833
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1799+511C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCA | 79 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0126others(76): Show | 79 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1799+511_1799+512i others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCACCTC others(149): Show |
17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+511_1799+512i others(158): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCACCTC others(331): Show |
1 | a0007c0008t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1799+511_1799+512i others(340): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGCTC others(352): Show |
1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1799+511_1799+512i others(361): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGCTC others(282): Show |
1 | a0001c0001t0001g0194 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1799+511_1799+512i others(291): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGCTC others(280): Show |
1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1799+511_1799+512i others(289): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGCTC others(283): Show |
1 | a0001c0001t0001g0178 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1799+511_1799+512i others(292): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGCTC others(282): Show |
140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 142 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1799+511_1799+512i others(291): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGCTC others(282): Show |
1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1799+511_1799+512i others(291): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGCTC others(268): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0188 | 2 | HG02622.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1799+511_1799+512i others(277): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGTTT others(275): Show |
4 | a0002c0003t0001g0005a0002c0003t0001g0275a0002c0003t0001g0281others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1799+511_1799+512i others(284): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCAGTTT others(331): Show |
3 | a0001c0004t0002g0061a0001c0004t0002g0069a0006c0009t0002g0072 | 3 | HG02055.hp2 HG02145.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1799+511_1799+512i others(340): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCGGCTC others(30): Show |
37 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(34): Show | 38 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1799+511_1799+512i others(39): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCGGCTC others(275): Show |
3 | a0001c0001t0001g0163a0001c0001t0001g0186a0001c0001t0001g0192 | 3 | HG01884.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1799+511_1799+512i others(284): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCGGCTC others(31): Show |
1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1799+511_1799+512i others(40): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907833
|
C | CCCTCCTC others(436): Show |
1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+511_1799+512i others(445): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907833 | ||||||
| chr16:89907856
|
A | G | 1 | a0009c0013t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1799+534A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907856 | ||||||
| chr16:89907872
|
TC | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0164a0007c0008t0001g0056 | 3 | HG00733.hp1 HG02698.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1799+553delC | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907872 | |||||
| chr16:89907877
|
G | C | 1 | a0009c0013t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1799+555G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907877 | ||||||
| chr16:89907878
|
T | C | 1 | a0009c0013t0002g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1799+556T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907878 | ||||||
| chr16:89907884
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1799+562C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907884 | ||||||
| chr16:89907884
|
CCTCCCAG | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 43 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1799+568_1799+574d others(9): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89907884 | |||||
| chr16:89907890
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1799+568A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907890 | ||||||
| chr16:89907891
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1799+569G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907891 | ||||||
| chr16:89907959
|
C | T | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+637C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89907959 | ||||||
| chr16:89908009
|
G | C | 7 | a0001c0001t0001g0098a0002c0003t0001g0285a0002c0003t0001g0286others(4): Show | 7 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+687G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908009 | ||||||
| chr16:89908019
|
T | C | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+697T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908019 | ||||||
| chr16:89908052
|
G | C | 6 | a0001c0001t0001g0007a0002c0003t0001g0276a0002c0003t0001g0278others(3): Show | 6 | HG01167.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1799+730G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908052 | ||||||
| chr16:89908090
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1799+768C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908090 | ||||||
| chr16:89908177
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1799+855C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908177 | ||||||
| chr16:89908184
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1799+862C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908184 | ||||||
| chr16:89908185
|
G | A | 1 | a0001c0004t0002g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1799+863G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908185 | ||||||
| chr16:89908197
|
C | T | 30 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(27): Show | 30 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.1799+875C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908197 | ||||||
| chr16:89908229
|
TCTCAGTT others(9): Show |
T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+909_1799+924d others(18): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908229 | |||||
| chr16:89908230
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1799+908C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908230 | ||||||
| chr16:89908235
|
TTCCCACC others(7): Show |
T | 58 | a0001c0001t0001g0133a0001c0001t0001g0154a0001c0001t0001g0161others(55): Show | 58 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1799+932_1799+945d others(16): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908235 | |||||
| chr16:89908249
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+927C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908249 | ||||||
| chr16:89908270
|
T | C | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 98 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1799+948T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908270 | ||||||
| chr16:89908316
|
T | TAGTTCTT others(102): Show |
7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+999_1799+1000 others(112): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908316 | |||||
| chr16:89908321
|
CCCA | C | 48 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(45): Show | 48 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1799+1001_1799+100 others(7): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908321 | |||||
| chr16:89908325
|
C | T | 48 | a0001c0002t0001g0021a0001c0002t0001g0022a0001c0002t0001g0023others(45): Show | 48 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1799+1003C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908325 | ||||||
| chr16:89908326
|
T | C | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+1004T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908326 | ||||||
| chr16:89908329
|
T | C | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+1007T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908329 | ||||||
| chr16:89908336
|
A | G | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+1014A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908336 | ||||||
| chr16:89908389
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1067C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908389 | ||||||
| chr16:89908391
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(19): Show | 23 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1799+1069T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908391 | ||||||
| chr16:89908475
|
G | A | 7 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(4): Show | 7 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1799+1153G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908475 | ||||||
| chr16:89908587
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1799+1265C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908587 | ||||||
| chr16:89908596
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0001t0001g0098others(23): Show | 27 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1799+1274C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908596 | ||||||
| chr16:89908597
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1799+1275G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908597 | ||||||
| chr16:89908597
|
GCCTCCCT | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0077others(11): Show | 15 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1799+1282_1799+128 others(11): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908597 | |||||
| chr16:89908604
|
T | A | 13 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1799+1282T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908604 | ||||||
| chr16:89908605
|
C | G | 12 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0087others(9): Show | 12 | HG00323.hp2 HG00733.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1799+1283C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908605 | ||||||
| chr16:89908612
|
G | C | 12 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0087others(9): Show | 12 | HG00323.hp2 HG00733.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1799+1290G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908612 | ||||||
| chr16:89908626
|
G | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0161 | 2 | NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1799+1304G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908626 | ||||||
| chr16:89908633
|
C | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0161 | 2 | NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1799+1311C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908633 | ||||||
| chr16:89908639
|
A | T | 56 | a0001c0001t0001g0117a0001c0001t0001g0265a0001c0001t0001g0270others(53): Show | 56 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1799+1317A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908639 | ||||||
| chr16:89908640
|
C | G | 13 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1799+1318C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908640 | ||||||
| chr16:89908647
|
G | C | 13 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG00323.hp2 HG00733.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1799+1325G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908647 | ||||||
| chr16:89908653
|
A | ACCTCCCT | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1799+1337_1799+133 others(11): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908653 | |||||
| chr16:89908653
|
A | T | 14 | a0001c0001t0001g0062a0001c0001t0001g0086a0001c0001t0001g0087others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1799+1331A>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908653 | ||||||
| chr16:89908667
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1799+1345A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908667 | ||||||
| chr16:89908669
|
C | CTCCCACC others(546): Show |
13 | a0001c0004t0002g0058a0001c0004t0002g0061a0001c0004t0002g0063others(10): Show | 13 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1799+1351_1799+135 others(557): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908669 | |||||
| chr16:89908669
|
C | CTCCCACC others(546): Show |
3 | a0001c0004t0002g0059a0001c0004t0002g0071a0001c0004t0002g0263 | 3 | HG02622.hp2 HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1799+1351_1799+135 others(557): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908669 | |||||
| chr16:89908669
|
C | CTCCCACC others(546): Show |
1 | a0002c0006t0002g0190 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1799+1351_1799+135 others(557): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908669 | |||||
| chr16:89908669
|
C | CTCCCACC others(532): Show |
1 | a0001c0004t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1799+1351_1799+135 others(543): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908669 | |||||
| chr16:89908674
|
T | A | 18 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0061others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1799+1352T>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908674 | ||||||
| chr16:89908674
|
T | TCCTCCCA others(616): Show |
5 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0096others(2): Show | 5 | HG00733.hp2 HG02293.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1799+1359_1799+136 others(627): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908674
|
T | TCCTCCCA others(554): Show |
1 | a0001c0002t0001g0049 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1799+1359_1799+136 others(565): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908674
|
T | TCCTCCCA others(553): Show |
27 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(24): Show | 27 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1799+1359_1799+136 others(564): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908674
|
T | TCCTCCCA others(623): Show |
6 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0005t0001g0266others(3): Show | 6 | HG03239.hp2 HG03669.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1799+1359_1799+136 others(634): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908674
|
T | TCCTCCCA others(624): Show |
1 | a0001c0005t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1799+1359_1799+136 others(635): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908674
|
T | TCCTCCCA others(553): Show |
1 | a0001c0002t0001g0022 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1799+1359_1799+136 others(564): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908674
|
T | TCCTCCCA others(651): Show |
1 | a0007c0008t0001g0056 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(662): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908674
|
T | TCCTCCCA others(637): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0161 | 2 | NA18970.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1799+1372_1799+137 others(648): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908674 | |||||
| chr16:89908675
|
C | CCTCCCAC others(637): Show |
6 | a0001c0001t0001g0086a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG01243.hp1 HG01256.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1799+1359_1799+136 others(648): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908675 | |||||
| chr16:89908675
|
C | CCTCCCAC others(644): Show |
2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1799+1359_1799+136 others(655): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908675 | |||||
| chr16:89908682
|
G | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 20 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1799+1360G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908682 | ||||||
| chr16:89908688
|
A | ACCTCCCT others(665): Show |
2 | a0001c0001t0001g0181a0001c0001t0001g0189 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1799+1372_1799+137 others(676): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908688
|
A | ACCTCCCT others(686): Show |
75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0114others(72): Show | 77 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1799+1372_1799+137 others(697): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908688
|
A | ACCTCCCT others(679): Show |
1 | a0001c0001t0001g0218 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(690): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908688
|
A | ACCTCCCT others(686): Show |
1 | a0001c0001t0001g0193 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(697): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908688
|
A | ACCTCCCT others(687): Show |
2 | a0001c0001t0001g0209a0004c0012t0001g0257 | 2 | NA18940.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1799+1372_1799+137 others(698): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908688
|
A | ACCTCCCT others(686): Show |
1 | a0001c0001t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(697): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908688
|
A | ACCTCCCT others(689): Show |
1 | a0001c0001t0001g0247 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(700): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908688
|
A | ACCTTCCA others(21): Show |
1 | a0001c0001t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1799+1369_1799+137 others(32): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908688 | |||||
| chr16:89908689
|
C | CCTCCCAG others(819): Show |
1 | a0001c0001t0001g0111 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(830): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908689 | |||||
| chr16:89908689
|
C | CCTCCCTC others(658): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0074others(21): Show | 25 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1799+1372_1799+137 others(669): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908689 | |||||
| chr16:89908689
|
C | CCTCCCTC others(658): Show |
1 | a0001c0001t0001g0090 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(669): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908689 | |||||
| chr16:89908689
|
C | CCTCCCTC others(644): Show |
1 | a0001c0001t0001g0264 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(655): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908689 | |||||
| chr16:89908689
|
C | CCTCCCTC others(630): Show |
1 | a0002c0003t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(641): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908689 | |||||
| chr16:89908689
|
C | CCTCCCTC others(637): Show |
2 | a0002c0003t0001g0052a0002c0003t0001g0053 | 2 | HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1799+1372_1799+137 others(648): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908689 | |||||
| chr16:89908689
|
C | CCTTCCAG others(14): Show |
61 | a0001c0001t0001g0062a0001c0001t0001g0087a0001c0001t0001g0096others(58): Show | 61 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1799+1369_1799+137 others(25): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908689 | |||||
| chr16:89908689
|
C | G | 27 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 28 | HG00323.hp2 HG01109.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.1799+1367C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908689 | ||||||
| chr16:89908690
|
C | CTCCCTCC others(637): Show |
1 | a0001c0001t0001g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(648): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908690 | |||||
| chr16:89908690
|
C | CTCCCTCC others(630): Show |
1 | a0001c0001t0001g0115 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1799+1372_1799+137 others(641): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908690 | |||||
| chr16:89908690
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(16): Show | 20 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1799+1368C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908690 | ||||||
| chr16:89908695
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0250 | 2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1799+1373G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908695 | ||||||
| chr16:89908695
|
G | GCCTCCCA others(532): Show |
1 | a0001c0002t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1799+1380_1799+138 others(543): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908695 | |||||
| chr16:89908695
|
G | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0054others(88): Show | 91 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.1799+1373G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908695 | ||||||
| chr16:89908696
|
C | CCTCCCAC others(622): Show |
1 | a0001c0001t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1799+1380_1799+138 others(633): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908696 | |||||
| chr16:89908696
|
C | CCTCCCAC others(622): Show |
5 | a0002c0003t0001g0276a0002c0003t0001g0278a0002c0003t0001g0279others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1799+1380_1799+138 others(633): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908696 | |||||
| chr16:89908696
|
C | CCTCCCAC others(623): Show |
14 | a0001c0001t0001g0098a0001c0001t0001g0272a0002c0003t0001g0191others(11): Show | 14 | HG00639.hp1 HG02257.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1799+1380_1799+138 others(634): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908696 | |||||
| chr16:89908696
|
C | CCTCCCAC others(602): Show |
1 | a0002c0003t0001g0005 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1799+1380_1799+138 others(613): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908696 | |||||
| chr16:89908702
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0062others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1799+1380A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908702 | ||||||
| chr16:89908703
|
G | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1799+1381G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908703 | ||||||
| chr16:89908707
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1385C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908707 | ||||||
| chr16:89908709
|
A | G | 84 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0114others(81): Show | 86 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1799+1387A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908709 | ||||||
| chr16:89908710
|
C | CCTCCCTC others(669): Show |
1 | a0001c0001t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(680): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(673): Show |
1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(684): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(679): Show |
1 | a0001c0001t0001g0145 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(690): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(680): Show |
1 | a0001c0001t0001g0192 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(691): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(644): Show |
1 | a0001c0001t0001g0156 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(655): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(679): Show |
54 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0099others(51): Show | 54 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1799+1393_1799+139 others(690): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(672): Show |
6 | a0001c0001t0001g0054a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG01071.hp1 HG03041.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1799+1393_1799+139 others(683): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(672): Show |
1 | a0001c0001t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(683): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(673): Show |
1 | a0001c0001t0001g0116 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(684): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(665): Show |
1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(676): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(679): Show |
1 | a0001c0001t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(690): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(679): Show |
1 | a0001c0001t0001g0179 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(690): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTCCCTC others(700): Show |
1 | a0001c0001t0001g0291 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1799+1393_1799+139 others(711): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTTCCAG others(14): Show |
1 | a0001c0002t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1799+1390_1799+139 others(25): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | CCTTCCAG others(35): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0250 | 2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1799+1390_1799+139 others(46): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908710 | |||||
| chr16:89908710
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0057others(117): Show | 122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1799+1388C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908710 | ||||||
| chr16:89908716
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1394G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908716 | ||||||
| chr16:89908717
|
G | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1799+1395G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908717 | ||||||
| chr16:89908723
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1799+1401G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908723 | ||||||
| chr16:89908723
|
G | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1401G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908723 | ||||||
| chr16:89908730
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1799+1408A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908730 | ||||||
| chr16:89908731
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1799+1409G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908731 | ||||||
| chr16:89908731
|
G | GCTCCCGC others(7): Show |
21 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0272others(18): Show | 22 | HG00639.hp1 HG01167.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1799+1414_1799+141 others(18): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908731 | |||||
| chr16:89908731
|
G | GCTCCGCC others(6): Show |
1 | a0002c0003t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1799+1413_1799+141 others(17): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908731 | |||||
| chr16:89908732
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1410C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908732 | ||||||
| chr16:89908743
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1421T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908743 | ||||||
| chr16:89908744
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1422G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908744 | ||||||
| chr16:89908745
|
C | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1423C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908745 | ||||||
| chr16:89908755
|
G | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1433G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908755 | ||||||
| chr16:89908762
|
C | CCAACCTT others(336): Show |
17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1441_1799+144 others(347): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908762 | |||||
| chr16:89908790
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1468T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908790 | ||||||
| chr16:89908808
|
C | CCTCCCAA others(217): Show |
17 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(14): Show | 17 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799+1489_1799+149 others(228): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908808 | |||||
| chr16:89908808
|
C | G | 18 | a0001c0004t0002g0058a0001c0004t0002g0059a0001c0004t0002g0061others(15): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1799+1486C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908808 | ||||||
| chr16:89908812
|
G | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(32): Show | 35 | HG01109.hp1 HG01192.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1799+1490G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908812 | ||||||
| chr16:89908812
|
G | GCAGCTCC | 61 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0264others(58): Show | 62 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1799+1507_1799+151 others(11): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908812 | |||||
| chr16:89908812
|
G | GCAGCTCC others(7): Show |
1 | a0001c0002t0001g0045 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1799+1500_1799+151 others(18): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908812 | |||||
| chr16:89908812
|
GCAGCTCC | G | 20 | a0001c0001t0001g0126a0001c0001t0001g0168a0001c0001t0001g0197others(17): Show | 20 | HG00423.hp1 HG00673.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1799+1507_1799+151 others(11): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908812 | |||||
| chr16:89908826
|
CCAGCTCC others(7): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1799+1514_1799+152 others(18): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89908826 | |||||
| chr16:89908845
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1799+1523T>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908845 | ||||||
| chr16:89908991
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1800-1600G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89908991 | ||||||
| chr16:89909040
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1800-1551C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909040 | ||||||
| chr16:89909046
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0189 | 2 | HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1800-1545C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909046 | ||||||
| chr16:89909058
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0264others(22): Show | 26 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1800-1533C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909058 | ||||||
| chr16:89909065
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0099a0001c0001t0001g0165others(2): Show | 5 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1800-1526G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909065 | ||||||
| chr16:89909088
|
G | A | 55 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1800-1503G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909088 | ||||||
| chr16:89909114
|
A | G | 1 | a0002c0003t0001g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1800-1477A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909114 | ||||||
| chr16:89909147
|
G | C | 55 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1800-1444G>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909147 | ||||||
| chr16:89909164
|
A | G | 55 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(52): Show | 55 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1800-1427A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909164 | ||||||
| chr16:89909230
|
A | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1800-1361A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909230 | ||||||
| chr16:89909250
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0001g0033 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1800-1341G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909250 | ||||||
| chr16:89909277
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1800-1314C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909277 | ||||||
| chr16:89909320
|
G | T | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1800-1271G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909320 | ||||||
| chr16:89909398
|
C | A | 2 | a0002c0006t0002g0182a0002c0006t0002g0190 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1800-1193C>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909398 | ||||||
| chr16:89909465
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1800-1126C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909465 | ||||||
| chr16:89909488
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1800-1103C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909488 | ||||||
| chr16:89909489
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1800-1102G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909489 | ||||||
| chr16:89909503
|
C | G | 54 | a0001c0001t0001g0265a0001c0001t0001g0270a0001c0002t0001g0021others(51): Show | 54 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1800-1088C>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909503 | ||||||
| chr16:89909509
|
C | CA | 52 | a0001c0001t0001g0017a0001c0001t0001g0055a0001c0001t0001g0096others(49): Show | 52 | HG00423.hp1 HG01169.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.1800-1059dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89909509 | |||||
| chr16:89909509
|
C | CAA | 14 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | HG01192.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1800-1060_1800-105 others(6): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89909509 | |||||
| chr16:89909509
|
CA | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0057a0001c0001t0001g0075others(34): Show | 38 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1800-1059delA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89909509 | |||||
| chr16:89909558
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1800-1033G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909558 | ||||||
| chr16:89909620
|
G | A | 2 | a0001c0001t0001g0148a0001c0001t0001g0185 | 2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1800-971G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909620 | ||||||
| chr16:89909661
|
G | A | 1 | a0002c0003t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1800-930G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909661 | ||||||
| chr16:89909675
|
C | CA | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1800-896dupA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89909675 | |||||
| chr16:89909675
|
C | CAA | 13 | a0001c0001t0001g0062a0001c0001t0001g0085a0001c0001t0001g0086others(10): Show | 13 | HG01243.hp1 HG01256.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1800-897_1800-896d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89909675 | |||||
| chr16:89909675
|
CA | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0265a0001c0001t0001g0293others(21): Show | 25 | HG00621.hp2 HG01167.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1800-896delA | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89909675 | |||||
| chr16:89909675
|
CAA | C | 44 | a0001c0001t0001g0164a0001c0001t0001g0261a0001c0001t0001g0262others(41): Show | 44 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1800-897_1800-896d others(4): Show |
TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 89909675 | |||||
| chr16:89909767
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1800-824G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909767 | ||||||
| chr16:89909781
|
G | A | 32 | a0001c0001t0001g0098a0001c0001t0001g0265a0001c0001t0001g0270others(29): Show | 33 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.1800-810G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909781 | ||||||
| chr16:89909816
|
G | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 66 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1800-775G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909816 | ||||||
| chr16:89909921
|
G | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1800-670G>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909921 | ||||||
| chr16:89909924
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1800-667C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89909924 | ||||||
| chr16:89910076
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1800-515G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910076 | ||||||
| chr16:89910136
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1800-455T>C | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910136 | ||||||
| chr16:89910167
|
C | T | 1 | a0002c0003t0001g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1800-424C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910167 | ||||||
| chr16:89910192
|
A | G | 1 | a0001c0005t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1800-399A>G | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910192 | ||||||
| chr16:89910380
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0092 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1800-211C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910380 | ||||||
| chr16:89910430
|
C | T | 3 | a0001c0004t0002g0071a0001c0004t0002g0263a0002c0006t0002g0190 | 3 | HG02622.hp2 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1800-161C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910430 | ||||||
| chr16:89910431
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG01192.hp2 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1800-160G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910431 | ||||||
| chr16:89910496
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1800-95C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910496 | ||||||
| chr16:89910552
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0101 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1800-39G>A | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 16/17 | chr16 | 89910552 | ||||||
| chr16:89910764
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1872+101C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 17/17 | chr16 | 89910764 | ||||||
| chr16:89911074
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01074.hp2 | splice_region_variant&intron_variant | LOW | c.1873-6C>T | TCF25 | ENSG00000141002.20 | transcript | ENST00000263346.13 | protein_coding | 17/17 | chr16 | 89911074 |