Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 83439 |
|---|---|
| ensemblid | ENSG00000152284.5 |
| hgncid | 11640 |
| symbol | TCF7L1 |
| name | transcription factor 7 like 1 |
| refseq_nuc | NM_031283.3 |
| refseq_prot | NP_112573.1 |
| ensembl_nuc | ENST00000282111.4 |
| ensembl_prot | ENSP00000282111.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 85133392 |
| end | 85310387 |
| strand | + |
| ver | v1.2 |
| region | chr2:85133392-85310387 |
| region5000 | chr2:85128392-85315387 |
| regionname0 | TCF7L1_chr2_85133392_85310387 |
| regionname5000 | TCF7L1_chr2_85128392_85315387 |
| 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 | 1/0 | 588 | 131 | 39 | 30 | 44 | 5 | 12 | 30 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002 | 0/1 | 587 | 86 | 38 | 15 | 18 | 7 | 7 | 12 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0003 | 0/0 | 587 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0004 | 0/0 | 588 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0005 | 0/0 | 588 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0006 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0007 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0008 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0009 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0010 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0011 | 0/0 | 588 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0012 | 0/0 | 587 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0013 | 0/0 | 587 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| 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 | 1/0 | 1767 | 130 | 38 | 30 | 44 | 5 | 12 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0002 | 0/1 | 1764 | 84 | 36 | 15 | 18 | 7 | 7 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0003 | 0/0 | 1764 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0004 | 0/0 | 1767 | 3 | 0 | 2 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0005 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0006 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0007 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0008 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0009 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0010 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0011 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0012 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0013 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0014 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0015 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0016 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| c0017 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1219 | 136 | 48 | 26 | 41 | 6 | 15 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0002 | 1/1 | 1219 | 70 | 35 | 13 | 14 | 2 | 4 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0003 | 0/0 | 1219 | 15 | 1 | 4 | 7 | 2 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0004 | 0/0 | 1219 | 3 | 1 | 1 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0005 | 0/0 | 1219 | 3 | 0 | 2 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0006 | 0/0 | 1219 | 2 | 0 | 1 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0007 | 0/0 | 1219 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0008 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0009 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0010 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0011 | 0/0 | 1219 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| t0012 | 0/0 | 1219 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| 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 | 1/0 | 1767 | 130 | 38 | 30 | 44 | 5 | 12 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0001c0016 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002 | 0/1 | 1764 | 84 | 36 | 15 | 18 | 7 | 7 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0007 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0008 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0003c0003 | 0/0 | 1764 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0004c0004 | 0/0 | 1767 | 3 | 0 | 2 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0005c0005 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0005c0012 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0006c0006 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0007c0011 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0008c0013 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0009c0014 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0010c0015 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0011c0017 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0012c0010 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0013c0009 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2985 | 86 | 24 | 18 | 32 | 2 | 10 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0001c0001t0002 | 1/0 | 2985 | 37 | 14 | 8 | 11 | 1 | 2 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0001c0001t0005 | 0/0 | 2985 | 3 | 0 | 2 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0001c0001t0006 | 0/0 | 2985 | 2 | 0 | 1 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0001c0001t0007 | 0/0 | 2985 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0001c0001t0011 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0001c0016t0001 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002t0001 | 0/0 | 2982 | 43 | 20 | 7 | 7 | 4 | 5 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002t0002 | 0/1 | 2982 | 20 | 11 | 3 | 3 | 1 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002t0003 | 0/0 | 2982 | 15 | 1 | 4 | 7 | 2 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002t0004 | 0/0 | 2982 | 3 | 1 | 1 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002t0007 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002t0008 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0002t0012 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0007t0002 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0002c0008t0002 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0003c0003t0002 | 0/0 | 2982 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0004c0004t0002 | 0/0 | 2985 | 3 | 0 | 2 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0005c0005t0001 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0005c0005t0009 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0005c0012t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0006c0006t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0006c0006t0010 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0007c0011t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0008c0013t0001 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0009c0014t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0010c0015t0001 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0011c0017t0001 | 0/0 | 2985 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0012c0010t0001 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| a0013c0009t0001 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | copy fasta | chr2 | 85128392 | 85315387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0016t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0027 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0007t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0008t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0003c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0003c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0003c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0003c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0004c0004t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0004c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0004c0004t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0005c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0005c0005t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0005c0012t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0006c0006t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0006c0006t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0007c0011t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0008c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0009c0014t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0010c0015t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0011c0017t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0012c0010t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0013c0009t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0203 | EUR | FIN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00735 | hp2 | a0004 | c0004 | t0002 | g0142 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00741 | hp1 | a0002 | c0002 | t0004 | g0072 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01168 | hp2 | a0011 | c0017 | t0001 | g0220 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0114 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0068 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0064 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0074 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0050 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0051 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0073 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01952 | hp1 | a0002 | c0002 | t0003 | g0071 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0176 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0070 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02056 | hp2 | a0002 | c0002 | t0004 | g0055 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0080 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02135 | hp1 | a0008 | c0013 | t0001 | g0143 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02148 | hp2 | a0004 | c0004 | t0002 | g0123 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02165 | hp1 | a0010 | c0015 | t0001 | g0228 | EAS | CDX | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02257 | hp1 | a0009 | c0014 | t0002 | g0164 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02451 | hp1 | a0003 | c0003 | t0002 | g0036 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02451 | hp2 | a0002 | c0002 | t0012 | g0021 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02523 | hp2 | a0001 | c0001 | t0011 | g0116 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02572 | hp1 | a0003 | c0003 | t0002 | g0086 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02615 | hp1 | a0002 | c0008 | t0002 | g0041 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02615 | hp2 | a0005 | c0005 | t0001 | g0115 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02647 | hp1 | a0006 | c0006 | t0002 | g0108 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02647 | hp2 | a0002 | c0007 | t0002 | g0029 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02723 | hp1 | a0006 | c0006 | t0010 | g0233 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02895 | hp2 | a0013 | c0009 | t0001 | g0019 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02965 | hp2 | a0002 | c0002 | t0007 | g0006 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03041 | hp2 | a0005 | c0005 | t0009 | g0192 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0082 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03195 | hp1 | a0012 | c0010 | t0001 | g0207 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04115 | hp1 | a0004 | c0004 | t0002 | g0124 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0083 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0026 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18522 | hp2 | a0002 | c0002 | t0004 | g0085 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0146 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19030 | hp2 | a0005 | c0012 | t0002 | g0184 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19043 | hp1 | a0003 | c0003 | t0002 | g0197 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0235 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | ASW | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | ASW | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0002 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0065 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0023 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | GIH | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | GIH | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02559 | hp1 | a0002 | c0002 | t0008 | g0059 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03471 | hp2 | a0007 | c0011 | t0002 | g0231 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA21309 | hp2 | a0001 | c0016 | t0001 | g0186 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0027 | REF | REF | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0213 | REF | REF | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85133705
|
GGGC | G | 4 | a0002a0003a0012others(1): Show | 92 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(89): Show |
conservative_inframe_deletion | MODERATE | c.40_42delGGC | p.Gly14del | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | 333/2985 | 40/1767 | 14/588 | INFO_REALIGN_3_PRIME | chr2 | 85133705 | |
| chr2:85134038
|
T | C | 1 | a0007 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.272T>C | p.Val91Ala | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 2/12 | 565/2985 | 272/1767 | 91/588 | chr2 | 85134038 | ||
| chr2:85283531
|
T | A | 2 | a0003a0005 | 7 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
missense_variant | MODERATE | c.478T>A | p.Ser160Thr | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/12 | 771/2985 | 478/1767 | 160/588 | chr2 | 85283531 | ||
| chr2:85303946
|
C | G | 1 | a0012 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.710C>G | p.Ser237Cys | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 6/12 | 1003/2985 | 710/1767 | 237/588 | chr2 | 85303946 | ||
| chr2:85305288
|
A | G | 1 | a0011 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.874A>G | p.Met292Val | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/12 | 1167/2985 | 874/1767 | 292/588 | chr2 | 85305288 | ||
| chr2:85305331
|
C | T | 1 | a0013 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.917C>T | p.Pro306Leu | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/12 | 1210/2985 | 917/1767 | 306/588 | chr2 | 85305331 | ||
| chr2:85309235
|
C | A | 1 | a0008 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1540C>A | p.Gln514Lys | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1833/2985 | 1540/1767 | 514/588 | chr2 | 85309235 | ||
| chr2:85309241
|
G | T | 1 | a0010 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1546G>T | p.Ala516Ser | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1839/2985 | 1546/1767 | 516/588 | chr2 | 85309241 | ||
| chr2:85309292
|
G | A | 1 | a0004 | 3 | HG00735.hp2 HG02148.hp2 HG04115.hp1 |
missense_variant | MODERATE | c.1597G>A | p.Gly533Arg | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1890/2985 | 1597/1767 | 533/588 | chr2 | 85309292 | ||
| chr2:85309385
|
G | A | 1 | a0006 | 2 | HG02647.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.1690G>A | p.Ala564Thr | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1983/2985 | 1690/1767 | 564/588 | chr2 | 85309385 | ||
| chr2:85309442
|
G | A | 1 | a0009 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1747G>A | p.Val583Ile | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 2040/2985 | 1747/1767 | 583/588 | chr2 | 85309442 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85306251
|
C | T | 2 | a0001c0016a0005c0005 | 3 | HG02615.hp2 HG03041.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1035C>T | p.His345His | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 9/12 | 1328/2985 | 1035/1767 | 345/588 | chr2 | 85306251 | ||
| chr2:85309111
|
C | T | 1 | a0002c0008 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.1416C>T | p.His472His | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1709/2985 | 1416/1767 | 472/588 | chr2 | 85309111 | ||
| chr2:85309318
|
C | T | 1 | a0002c0007 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1623C>T | p.Leu541Leu | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1916/2985 | 1623/1767 | 541/588 | chr2 | 85309318 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85133494
|
C | T | 1 | a0002c0002t0012 | 1 | HG02451.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-191C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | chr2 | 85133494 | ||||||
| chr2:85133531
|
G | A | 3 | a0002c0002t0003a0002c0002t0004a0002c0002t0008 | 19 | HG00741.hp1 HG01257.hp1 HG01515.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-154G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | 154 | chr2 | 85133531 | |||||
| chr2:85133640
|
C | A | 2 | a0001c0001t0005a0001c0001t0006 | 5 | HG00639.hp1 HG01168.hp1 HG01261.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-45C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | 45 | chr2 | 85133640 | |||||
| chr2:85309603
|
C | T | 2 | a0001c0001t0007a0002c0002t0007 | 2 | HG01256.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 141 | chr2 | 85309603 | |||||
| chr2:85309827
|
C | T | 1 | a0001c0001t0011 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 365 | chr2 | 85309827 | |||||
| chr2:85309887
|
G | A | 3 | a0001c0001t0007a0002c0002t0007a0002c0002t0008 | 3 | HG01256.hp1 HG02559.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*425G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 425 | chr2 | 85309887 | |||||
| chr2:85310075
|
G | A | 1 | a0005c0005t0009 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 613 | chr2 | 85310075 | |||||
| chr2:85310189
|
G | A | 15 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(12): Show | 157 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*727G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 727 | chr2 | 85310189 | |||||
| chr2:85310222
|
G | A | 1 | a0006c0006t0010 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 760 | chr2 | 85310222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85133974
|
T | TGCGTCCG others(1): Show |
8 | a0002c0002t0001g0007a0002c0002t0001g0009a0002c0002t0001g0010others(5): Show | 8 | HG02145.hp1 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-41_250-34dupGC others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 85133974 | |||||
| chr2:85133978
|
T | G | 5 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0004others(2): Show | 5 | HG00639.hp1 HG01168.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-38T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/11 | chr2 | 85133978 | ||||||
| chr2:85134138
|
C | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+59C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 2/11 | chr2 | 85134138 | ||||||
| chr2:85134227
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | NA18950.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.314-96G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 2/11 | chr2 | 85134227 | ||||||
| chr2:85134728
|
C | T | 1 | a0002c0002t0003g0235 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.441+278C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85134728 | ||||||
| chr2:85134729
|
G | A | 7 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0006g0003others(4): Show | 7 | HG01261.hp2 HG01516.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+279G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85134729 | ||||||
| chr2:85135216
|
T | C | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.441+766T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135216 | ||||||
| chr2:85135622
|
G | A | 1 | a0002c0002t0012g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.441+1172G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135622 | ||||||
| chr2:85135702
|
G | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.441+1252G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135702 | ||||||
| chr2:85135788
|
G | A | 1 | a0002c0002t0002g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.441+1338G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135788 | ||||||
| chr2:85135789
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.441+1339G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135789 | ||||||
| chr2:85135790
|
A | AGGTC | 50 | a0001c0001t0001g0031a0001c0001t0002g0067a0001c0001t0005g0004others(47): Show | 50 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.441+1341_441+1344d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85135790 | |||||
| chr2:85135810
|
T | G | 10 | a0001c0001t0001g0031a0001c0001t0005g0004a0001c0001t0006g0005others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+1360T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135810 | ||||||
| chr2:85135931
|
AG | A | 101 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0091others(98): Show | 101 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.441+1492delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85135931 | |||||
| chr2:85135931
|
AGG | A | 82 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(79): Show | 82 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.441+1491_441+1492d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85135931 | |||||
| chr2:85135933
|
G | A | 7 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0006g0003others(4): Show | 7 | HG01261.hp2 HG01516.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+1483G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135933 | ||||||
| chr2:85135935
|
G | C | 19 | a0001c0001t0001g0076a0002c0002t0001g0069a0002c0002t0001g0081others(16): Show | 19 | HG00741.hp1 HG01257.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+1485G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135935 | ||||||
| chr2:85136034
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+1584C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136034 | ||||||
| chr2:85136466
|
CCAACCTT others(4): Show |
C | 1 | a0002c0002t0012g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.441+2018_441+2028d others(13): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85136466 | |||||
| chr2:85136520
|
G | A | 3 | a0002c0002t0001g0032a0002c0002t0001g0033a0002c0002t0001g0034 | 3 | HG02818.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.441+2070G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136520 | ||||||
| chr2:85136583
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.441+2133G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136583 | ||||||
| chr2:85136615
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.441+2165T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136615 | ||||||
| chr2:85136709
|
G | C | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+2259G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136709 | ||||||
| chr2:85136832
|
T | C | 1 | a0002c0002t0003g0068 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.441+2382T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136832 | ||||||
| chr2:85136970
|
C | T | 42 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(39): Show | 42 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.441+2520C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136970 | ||||||
| chr2:85137015
|
C | T | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+2565C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137015 | ||||||
| chr2:85137184
|
T | G | 37 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0032others(34): Show | 37 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.441+2734T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137184 | ||||||
| chr2:85137414
|
G | A | 29 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0183others(26): Show | 29 | HG00741.hp1 HG01257.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.441+2964G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137414 | ||||||
| chr2:85137566
|
T | C | 79 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0170others(76): Show | 79 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.441+3116T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137566 | ||||||
| chr2:85137630
|
G | C | 36 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0032others(33): Show | 36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+3180G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137630 | ||||||
| chr2:85137646
|
A | G | 11 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(8): Show | 11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+3196A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137646 | ||||||
| chr2:85137682
|
C | T | 36 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0032others(33): Show | 36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+3232C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137682 | ||||||
| chr2:85137701
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG00597.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.441+3251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137701 | ||||||
| chr2:85137892
|
CA | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0232a0001c0001t0001g0234others(5): Show | 8 | HG01167.hp1 HG01168.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+3459delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85137892 | |||||
| chr2:85137906
|
A | G | 2 | a0002c0002t0002g0020a0002c0002t0002g0065 | 2 | HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.441+3456A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137906 | ||||||
| chr2:85138244
|
C | T | 36 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0032others(33): Show | 36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+3794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138244 | ||||||
| chr2:85138375
|
A | G | 108 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0090others(105): Show | 108 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(105): Show |
intron_variant | MODIFIER | c.441+3925A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138375 | ||||||
| chr2:85138394
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+3944T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138394 | ||||||
| chr2:85138446
|
G | A | 10 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(7): Show | 10 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+3996G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138446 | ||||||
| chr2:85138492
|
TTC | T | 2 | a0002c0002t0001g0087a0005c0012t0002g0184 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+4044_441+4045d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85138492 | |||||
| chr2:85138588
|
C | T | 36 | a0002c0002t0001g0022a0002c0002t0001g0023a0002c0002t0001g0032others(33): Show | 36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+4138C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138588 | ||||||
| chr2:85138843
|
C | T | 2 | a0001c0001t0002g0067a0003c0003t0002g0086 | 2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.441+4393C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138843 | ||||||
| chr2:85138863
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.441+4413G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138863 | ||||||
| chr2:85139195
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.441+4745G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139195 | ||||||
| chr2:85139703
|
C | G | 1 | a0002c0002t0001g0064 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.441+5253C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139703 | ||||||
| chr2:85139831
|
G | C | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441+5381G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139831 | ||||||
| chr2:85139848
|
T | G | 78 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0170others(75): Show | 78 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.441+5398T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139848 | ||||||
| chr2:85139864
|
T | G | 22 | a0001c0001t0001g0092a0001c0001t0001g0170a0001c0001t0001g0171others(19): Show | 22 | HG01175.hp2 HG01256.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.441+5414T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139864 | ||||||
| chr2:85139958
|
G | A | 21 | a0001c0001t0001g0092a0001c0001t0001g0170a0001c0001t0001g0171others(18): Show | 21 | HG01175.hp2 HG01256.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+5508G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139958 | ||||||
| chr2:85140088
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+5638G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140088 | ||||||
| chr2:85140155
|
C | T | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+5705C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140155 | ||||||
| chr2:85140201
|
A | G | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+5751A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140201 | ||||||
| chr2:85140480
|
T | TC | 165 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0088others(162): Show | 165 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.441+6032dupC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85140480 | |||||
| chr2:85140501
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+6051G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140501 | ||||||
| chr2:85140605
|
C | T | 5 | a0002c0002t0001g0089a0002c0002t0002g0016a0002c0002t0002g0018others(2): Show | 5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+6155C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140605 | ||||||
| chr2:85140619
|
TG | T | 208 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(205): Show | 208 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(205): Show |
intron_variant | MODIFIER | c.441+6171delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85140619 | |||||
| chr2:85140685
|
G | A | 29 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0170others(26): Show | 29 | HG01071.hp2 HG01175.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.441+6235G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140685 | ||||||
| chr2:85140732
|
G | A | 111 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0091others(108): Show | 111 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.441+6282G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140732 | ||||||
| chr2:85140767
|
A | G | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+6317A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140767 | ||||||
| chr2:85140896
|
C | T | 1 | a0002c0002t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.441+6446C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140896 | ||||||
| chr2:85140899
|
A | G | 1 | a0002c0002t0003g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.441+6449A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140899 | ||||||
| chr2:85140904
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0234a0006c0006t0010g0233 | 3 | HG02723.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.441+6454A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140904 | ||||||
| chr2:85140913
|
C | CAGAG | 161 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(158): Show | 161 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.441+6466_441+6467i others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85140913 | |||||
| chr2:85140939
|
C | T | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+6489C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140939 | ||||||
| chr2:85140967
|
G | C | 31 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0170others(28): Show | 31 | HG01071.hp2 HG01175.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+6517G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140967 | ||||||
| chr2:85141127
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.441+6677A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141127 | ||||||
| chr2:85141205
|
A | T | 15 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(12): Show | 15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+6755A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141205 | ||||||
| chr2:85141220
|
C | CAG | 190 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(187): Show | 190 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(187): Show |
intron_variant | MODIFIER | c.441+6771_441+6772d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85141220 | |||||
| chr2:85141282
|
A | G | 2 | a0001c0001t0001g0088a0003c0003t0002g0086 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.441+6832A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141282 | ||||||
| chr2:85141443
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.441+6993G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141443 | ||||||
| chr2:85141510
|
A | G | 4 | a0002c0002t0001g0057a0002c0002t0002g0017a0002c0002t0002g0058others(1): Show | 4 | HG02559.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+7060A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141510 | ||||||
| chr2:85141625
|
A | T | 15 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(12): Show | 15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+7175A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141625 | ||||||
| chr2:85141856
|
T | A | 6 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(3): Show | 6 | HG02257.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+7406T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141856 | ||||||
| chr2:85142034
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+7584T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142034 | ||||||
| chr2:85142137
|
C | T | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(6): Show | 9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+7687C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142137 | ||||||
| chr2:85142169
|
G | A | 1 | a0002c0002t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+7719G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142169 | ||||||
| chr2:85142195
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+7745G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142195 | ||||||
| chr2:85142258
|
T | C | 160 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(157): Show | 160 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.441+7808T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142258 | ||||||
| chr2:85142340
|
G | A | 1 | a0002c0002t0003g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.441+7890G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142340 | ||||||
| chr2:85142431
|
AATGTGTG others(8): Show |
A | 2 | a0002c0002t0001g0087a0005c0012t0002g0184 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+7982_441+7996d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142431 | ||||||
| chr2:85142432
|
ATGTG | A | 24 | a0001c0001t0001g0160a0001c0001t0001g0218a0001c0001t0001g0219others(21): Show | 24 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+8012_441+8015d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | |||||
| chr2:85142432
|
ATGTGTG | A | 15 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0002g0147others(12): Show | 15 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.441+8010_441+8015d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | |||||
| chr2:85142432
|
ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.441+8002_441+8015d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | |||||
| chr2:85142432
|
ATGTGTGT others(8): Show |
A | 14 | a0001c0001t0001g0090a0001c0001t0002g0167a0002c0002t0001g0007others(11): Show | 14 | HG00735.hp1 HG02145.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+7983_441+7997d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142432 | ||||||
| chr2:85142432
|
ATGTGTGT others(9): Show |
A | 165 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(162): Show | 165 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.441+8000_441+8015d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | |||||
| chr2:85142432
|
ATGTGTGT others(11): Show |
A | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG00597.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.441+7998_441+8015d others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | |||||
| chr2:85142433
|
TGTGTGTG others(12): Show |
T | 7 | a0001c0001t0002g0067a0002c0002t0001g0089a0002c0002t0002g0016others(4): Show | 7 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+7984_441+8002d others(21): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142433 | ||||||
| chr2:85142448
|
G | A | 14 | a0001c0001t0001g0090a0001c0001t0002g0167a0002c0002t0001g0007others(11): Show | 14 | HG00735.hp1 HG02145.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+7998G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142448 | ||||||
| chr2:85142455
|
T | A | 2 | a0002c0002t0001g0057a0002c0002t0002g0058 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.441+8005T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142455 | ||||||
| chr2:85142481
|
A | AAT | 8 | a0001c0001t0001g0145a0001c0001t0002g0067a0002c0002t0001g0089others(5): Show | 8 | HG01109.hp1 HG02451.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+8047_441+8048d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142481 | |||||
| chr2:85142481
|
A | AATAT | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(8): Show | 11 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.441+8045_441+8048d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142481 | |||||
| chr2:85142482
|
A | T | 15 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(12): Show | 15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+8032A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142482 | ||||||
| chr2:85142693
|
C | T | 9 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0040others(6): Show | 9 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+8243C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142693 | ||||||
| chr2:85142753
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+8303T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142753 | ||||||
| chr2:85143284
|
T | C | 6 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+8834T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143284 | ||||||
| chr2:85143442
|
TA | T | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+8994delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85143442 | |||||
| chr2:85143593
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.441+9143C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143593 | ||||||
| chr2:85143645
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.441+9195G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143645 | ||||||
| chr2:85143696
|
G | A | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+9246G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143696 | ||||||
| chr2:85143790
|
T | C | 18 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0163others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+9340T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143790 | ||||||
| chr2:85144047
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.441+9597G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144047 | ||||||
| chr2:85144103
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.441+9653A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144103 | ||||||
| chr2:85144178
|
T | C | 9 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0040others(6): Show | 9 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+9728T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144178 | ||||||
| chr2:85144417
|
C | CA | 9 | a0001c0001t0001g0218a0001c0001t0005g0001a0002c0002t0001g0024others(6): Show | 9 | HG00741.hp1 HG01261.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+9984dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144417 | |||||
| chr2:85144417
|
C | CAA | 11 | a0001c0001t0001g0099a0001c0001t0002g0067a0001c0001t0002g0100others(8): Show | 11 | HG01071.hp2 HG01884.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+9983_441+9984d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144417 | |||||
| chr2:85144417
|
CA | C | 136 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(133): Show | 136 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.441+9984delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144417 | |||||
| chr2:85144435
|
C | A | 31 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0170others(28): Show | 31 | HG01071.hp2 HG01175.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+9985C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144435 | ||||||
| chr2:85144611
|
A | T | 5 | a0001c0001t0001g0099a0001c0001t0002g0100a0002c0002t0001g0087others(2): Show | 5 | HG03139.hp1 HG03139.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+10161A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144611 | ||||||
| chr2:85144705
|
TTC | T | 77 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0091others(74): Show | 77 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.441+10269_441+1027 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144705 | |||||
| chr2:85144705
|
TTCTC | T | 21 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0101others(18): Show | 21 | HG00597.hp1 HG00639.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+10267_441+1027 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144705 | |||||
| chr2:85144705
|
TTCTCTC | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+10265_441+1027 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144705 | |||||
| chr2:85144713
|
C | G | 2 | a0001c0001t0001g0180a0002c0002t0001g0056 | 2 | NA18951.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.441+10263C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144713 | ||||||
| chr2:85144715
|
C | G | 28 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0109others(25): Show | 28 | HG01106.hp2 HG01167.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+10265C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144715 | ||||||
| chr2:85144717
|
C | G | 98 | a0001c0001t0001g0015a0001c0001t0001g0091a0001c0001t0001g0097others(95): Show | 98 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.441+10267C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144717 | ||||||
| chr2:85144719
|
C | CTCTCTG | 4 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0045others(1): Show | 4 | HG01071.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+10270_441+1027 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | |||||
| chr2:85144719
|
C | CTCTCTGT others(1): Show |
5 | a0002c0002t0001g0040a0002c0002t0001g0042a0002c0002t0002g0043others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+10270_441+1027 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | |||||
| chr2:85144719
|
C | CTG | 14 | a0001c0001t0001g0031a0001c0001t0001g0229a0001c0001t0001g0230others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+10299_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | |||||
| chr2:85144719
|
C | G | 130 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(127): Show | 130 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.441+10269C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144719 | ||||||
| chr2:85144719
|
CTG | C | 2 | a0001c0001t0001g0219a0002c0002t0003g0084 | 2 | HG01071.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.441+10299_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | |||||
| chr2:85144721
|
G | C | 10 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0100others(7): Show | 10 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+10271G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144721 | ||||||
| chr2:85144723
|
G | C | 6 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+10273G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144723 | ||||||
| chr2:85144749
|
G | GTGTGTGT others(1): Show |
6 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(3): Show | 6 | HG02257.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+10300_441+1030 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | |||||
| chr2:85144749
|
G | GTGTGTT | 2 | a0002c0002t0002g0062a0002c0002t0002g0066 | 2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.441+10300_441+1030 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | |||||
| chr2:85144749
|
G | GTGTT | 16 | a0001c0001t0001g0090a0001c0001t0001g0107a0002c0002t0001g0007others(13): Show | 16 | HG01109.hp1 HG02145.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+10300_441+1030 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | |||||
| chr2:85144749
|
G | GTT | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 6 | HG01891.hp2 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+10300_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | |||||
| chr2:85144749
|
G | T | 112 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0091others(109): Show | 112 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.441+10299G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144749 | ||||||
| chr2:85144749
|
GTA | G | 3 | a0001c0001t0001g0099a0001c0001t0002g0100a0002c0002t0001g0087 | 3 | HG03139.hp2 HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+10301_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | |||||
| chr2:85144751
|
A | G | 159 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(156): Show | 159 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.441+10301A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144751 | ||||||
| chr2:85144806
|
G | A | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+10356G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144806 | ||||||
| chr2:85144816
|
G | A | 3 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0006g0003 | 3 | HG01261.hp2 HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.441+10366G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144816 | ||||||
| chr2:85144854
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.441+10404C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144854 | ||||||
| chr2:85144971
|
G | A | 142 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(139): Show | 142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+10521G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144971 | ||||||
| chr2:85144978
|
G | A | 18 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0163others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+10528G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144978 | ||||||
| chr2:85145016
|
C | T | 124 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0091others(121): Show | 124 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.441+10566C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145016 | ||||||
| chr2:85145107
|
C | T | 13 | a0001c0001t0001g0031a0001c0001t0002g0098a0001c0001t0002g0147others(10): Show | 13 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+10657C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145107 | ||||||
| chr2:85145251
|
T | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0232a0001c0001t0001g0234others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+10801T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145251 | ||||||
| chr2:85145410
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+10960A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145410 | ||||||
| chr2:85145499
|
C | G | 1 | a0002c0002t0004g0055 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.441+11049C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145499 | ||||||
| chr2:85145546
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0217 | 2 | HG00280.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.441+11096G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145546 | ||||||
| chr2:85145582
|
G | A | 4 | a0001c0001t0001g0099a0001c0001t0002g0100a0002c0002t0001g0087others(1): Show | 4 | HG03139.hp2 HG03669.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+11132G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145582 | ||||||
| chr2:85145615
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.441+11165G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145615 | ||||||
| chr2:85145884
|
A | T | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+11434A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145884 | ||||||
| chr2:85146054
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.441+11604C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146054 | ||||||
| chr2:85146492
|
T | C | 15 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(12): Show | 15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+12042T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146492 | ||||||
| chr2:85146497
|
C | CT | 9 | a0001c0001t0001g0088a0001c0001t0001g0170a0001c0001t0001g0171others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+12068dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85146497 | |||||
| chr2:85146497
|
CT | C | 24 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0100others(21): Show | 24 | HG00741.hp1 HG01071.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+12068delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85146497 | |||||
| chr2:85146497
|
CTTT | C | 135 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(132): Show | 135 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.441+12066_441+1206 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85146497 | |||||
| chr2:85146501
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.441+12051T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146501 | ||||||
| chr2:85146626
|
T | C | 176 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(173): Show | 176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+12176T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146626 | ||||||
| chr2:85146694
|
A | G | 145 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(142): Show | 145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+12244A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146694 | ||||||
| chr2:85146704
|
G | A | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+12254G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146704 | ||||||
| chr2:85146730
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.441+12280C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146730 | ||||||
| chr2:85146753
|
G | A | 4 | a0001c0001t0002g0106a0002c0002t0001g0032a0002c0002t0001g0033others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+12303G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146753 | ||||||
| chr2:85146755
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.441+12305C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146755 | ||||||
| chr2:85146775
|
A | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441+12325A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146775 | ||||||
| chr2:85146853
|
C | T | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+12403C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146853 | ||||||
| chr2:85147038
|
T | G | 3 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0006g0003 | 3 | HG01261.hp2 HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.441+12588T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147038 | ||||||
| chr2:85147074
|
G | A | 142 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(139): Show | 142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+12624G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147074 | ||||||
| chr2:85147138
|
GATAA | G | 13 | a0001c0001t0001g0031a0001c0001t0002g0098a0001c0001t0002g0147others(10): Show | 13 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+12694_441+1269 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85147138 | |||||
| chr2:85147192
|
A | C | 145 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(142): Show | 145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+12742A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147192 | ||||||
| chr2:85147288
|
G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.441+12838G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147288 | ||||||
| chr2:85147294
|
G | A | 142 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(139): Show | 142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+12844G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147294 | ||||||
| chr2:85147357
|
C | T | 173 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(170): Show | 173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+12907C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147357 | ||||||
| chr2:85147359
|
A | G | 173 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(170): Show | 173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+12909A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147359 | ||||||
| chr2:85147403
|
A | G | 142 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(139): Show | 142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+12953A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147403 | ||||||
| chr2:85147558
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.441+13108G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147558 | ||||||
| chr2:85147655
|
C | T | 27 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0148others(24): Show | 27 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.441+13205C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147655 | ||||||
| chr2:85147692
|
C | G | 1 | a0007c0011t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.441+13242C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147692 | ||||||
| chr2:85147700
|
C | T | 5 | a0002c0002t0001g0089a0002c0002t0002g0016a0002c0002t0002g0018others(2): Show | 5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+13250C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147700 | ||||||
| chr2:85147878
|
T | C | 176 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(173): Show | 176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+13428T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147878 | ||||||
| chr2:85147891
|
C | T | 1 | a0002c0002t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+13441C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147891 | ||||||
| chr2:85148009
|
T | G | 176 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(173): Show | 176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+13559T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148009 | ||||||
| chr2:85148068
|
T | G | 3 | a0001c0001t0001g0219a0002c0002t0002g0063a0011c0017t0001g0220 | 3 | HG01071.hp1 HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.441+13618T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148068 | ||||||
| chr2:85148159
|
G | A | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0067others(18): Show | 21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+13709G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148159 | ||||||
| chr2:85148216
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+13766G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148216 | ||||||
| chr2:85148451
|
G | A | 142 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(139): Show | 142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+14001G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148451 | ||||||
| chr2:85148473
|
A | T | 3 | a0001c0001t0002g0138a0002c0002t0002g0020a0002c0002t0002g0054 | 3 | HG01074.hp2 HG02145.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.441+14023A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148473 | ||||||
| chr2:85148553
|
C | T | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0067others(18): Show | 21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+14103C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148553 | ||||||
| chr2:85148771
|
A | AT | 113 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(110): Show | 113 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.441+14341dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85148771 | |||||
| chr2:85148771
|
A | ATTT | 10 | a0001c0001t0001g0099a0001c0001t0001g0170a0001c0001t0001g0171others(7): Show | 10 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+14339_441+1434 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85148771 | |||||
| chr2:85148771
|
AT | A | 7 | a0001c0001t0001g0149a0001c0001t0006g0005a0002c0002t0001g0037others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+14341delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85148771 | |||||
| chr2:85148923
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+14473C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148923 | ||||||
| chr2:85148998
|
T | C | 176 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(173): Show | 176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+14548T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148998 | ||||||
| chr2:85149071
|
G | A | 15 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(12): Show | 15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+14621G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149071 | ||||||
| chr2:85149109
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.441+14659A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149109 | ||||||
| chr2:85149283
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.441+14833A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149283 | ||||||
| chr2:85149303
|
A | ATATATGT others(25): Show |
6 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0230others(3): Show | 6 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+14861_441+1489 others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149303 | |||||
| chr2:85149326
|
C | CAT | 140 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(137): Show | 140 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.441+14879_441+1488 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149326 | |||||
| chr2:85149346
|
T | TAC | 20 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0067others(17): Show | 20 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.441+14907_441+1490 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149346 | |||||
| chr2:85149346
|
T | TACACAC | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+14903_441+1490 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149346 | |||||
| chr2:85149548
|
TAG | T | 2 | a0001c0001t0001g0216a0010c0015t0001g0228 | 2 | HG02165.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.441+15101_441+1510 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149548 | |||||
| chr2:85149692
|
T | C | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+15242T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149692 | ||||||
| chr2:85149804
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+15354C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149804 | ||||||
| chr2:85149817
|
G | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.441+15367G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149817 | ||||||
| chr2:85149827
|
G | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+15377G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149827 | ||||||
| chr2:85149847
|
T | C | 8 | a0001c0001t0002g0147a0001c0001t0002g0181a0001c0001t0005g0004others(5): Show | 8 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+15397T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149847 | ||||||
| chr2:85149947
|
G | A | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+15497G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149947 | ||||||
| chr2:85150056
|
T | C | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0067others(18): Show | 21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+15606T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150056 | ||||||
| chr2:85150315
|
C | G | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+15865C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150315 | ||||||
| chr2:85150357
|
C | A | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+15907C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150357 | ||||||
| chr2:85150382
|
C | A | 1 | a0001c0001t0001g0216 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.441+15932C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150382 | ||||||
| chr2:85150453
|
C | T | 145 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(142): Show | 145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+16003C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150453 | ||||||
| chr2:85150502
|
T | G | 3 | a0001c0001t0001g0188a0002c0002t0002g0048a0002c0002t0004g0055 | 3 | HG02056.hp2 HG02083.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.441+16052T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150502 | ||||||
| chr2:85150586
|
C | CT | 18 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0002g0100others(15): Show | 18 | HG00738.hp2 HG01074.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+16150dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85150586 | |||||
| chr2:85150586
|
CT | C | 5 | a0001c0001t0001g0150a0001c0001t0001g0156a0002c0002t0002g0016others(2): Show | 5 | HG01952.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+16150delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85150586 | |||||
| chr2:85150673
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.441+16223C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150673 | ||||||
| chr2:85150687
|
T | C | 26 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0148others(23): Show | 26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+16237T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150687 | ||||||
| chr2:85150751
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+16301T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150751 | ||||||
| chr2:85150856
|
A | G | 145 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(142): Show | 145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+16406A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150856 | ||||||
| chr2:85150901
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+16451C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150901 | ||||||
| chr2:85150971
|
C | T | 1 | a0002c0002t0002g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.441+16521C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150971 | ||||||
| chr2:85151028
|
T | A | 21 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0002g0067others(18): Show | 21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+16578T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151028 | ||||||
| chr2:85151125
|
T | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+16675T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151125 | ||||||
| chr2:85151172
|
C | T | 15 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(12): Show | 15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+16722C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151172 | ||||||
| chr2:85151540
|
T | A | 145 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(142): Show | 145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+17090T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151540 | ||||||
| chr2:85151543
|
C | A | 6 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+17093C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151543 | ||||||
| chr2:85151698
|
C | G | 173 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(170): Show | 173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+17248C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151698 | ||||||
| chr2:85151771
|
C | A | 119 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(116): Show | 119 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.441+17321C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151771 | ||||||
| chr2:85151779
|
G | T | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+17329G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151779 | ||||||
| chr2:85152234
|
C | G | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+17784C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152234 | ||||||
| chr2:85152435
|
C | CT | 107 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0091others(104): Show | 107 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.441+17986dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152435 | |||||
| chr2:85152435
|
C | CTT | 53 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0095others(50): Show | 53 | HG00597.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.441+17986_441+1798 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152435 | |||||
| chr2:85152435
|
C | CTTT | 10 | a0001c0001t0001g0099a0001c0001t0001g0171a0001c0001t0002g0100others(7): Show | 10 | HG01175.hp2 HG01258.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+17986_441+1798 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152435 | |||||
| chr2:85152437
|
C | T | 173 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(170): Show | 173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+17987C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152437 | ||||||
| chr2:85152476
|
C | T | 26 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0148others(23): Show | 26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+18026C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152476 | ||||||
| chr2:85152495
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.441+18045C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152495 | ||||||
| chr2:85152533
|
C | G | 163 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(160): Show | 163 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.441+18083C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152533 | ||||||
| chr2:85152606
|
C | T | 52 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0096others(49): Show | 52 | HG00597.hp1 HG00639.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.441+18156C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152606 | ||||||
| chr2:85152649
|
GGTCTTAA others(80): Show |
G | 26 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0148others(23): Show | 26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+18204_441+1829 others(91): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152649 | |||||
| chr2:85152669
|
G | A | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+18219G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152669 | ||||||
| chr2:85152768
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+18318G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152768 | ||||||
| chr2:85152791
|
T | C | 150 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(147): Show | 150 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.441+18341T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152791 | ||||||
| chr2:85152881
|
T | C | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+18431T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152881 | ||||||
| chr2:85152929
|
T | C | 26 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0148others(23): Show | 26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+18479T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152929 | ||||||
| chr2:85153016
|
A | G | 6 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0230others(3): Show | 6 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+18566A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153016 | ||||||
| chr2:85153070
|
C | T | 2 | a0002c0002t0001g0087a0005c0012t0002g0184 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+18620C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153070 | ||||||
| chr2:85153157
|
T | A | 1 | a0002c0002t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.441+18707T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153157 | ||||||
| chr2:85153339
|
A | C | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+18889A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153339 | ||||||
| chr2:85153340
|
A | AT | 6 | a0001c0001t0001g0076a0001c0001t0001g0160a0002c0002t0001g0013others(3): Show | 6 | HG01257.hp1 HG02486.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+18909dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATATTTTT others(24): Show |
1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.441+18891_441+1889 others(35): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATATTTTT others(25): Show |
2 | a0002c0002t0001g0007a0002c0002t0002g0008 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.441+18891_441+1889 others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATATTTTT others(26): Show |
1 | a0002c0002t0001g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.441+18891_441+1889 others(37): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATGTTTTT others(11): Show |
3 | a0001c0001t0002g0167a0001c0001t0002g0174a0001c0001t0002g0175 | 3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+18891_441+1889 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATGTTTTT others(12): Show |
3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166 | 3 | HG01256.hp2 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.441+18891_441+1889 others(23): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATGTTTTT others(13): Show |
1 | a0002c0002t0001g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.441+18891_441+1889 others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTT | 32 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0121others(29): Show | 32 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+18905_441+1890 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTT | 59 | a0001c0001t0001g0015a0001c0001t0001g0091a0001c0001t0001g0097others(56): Show | 59 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.441+18904_441+1890 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT | 6 | a0001c0001t0001g0113a0001c0001t0001g0135a0001c0001t0001g0196others(3): Show | 6 | HG01346.hp2 HG02056.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+18903_441+1890 others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0099a0001c0001t0001g0209a0001c0001t0002g0100others(1): Show | 4 | HG03540.hp2 HG03669.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+18900_441+1890 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(4): Show |
24 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0148others(21): Show | 24 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+18899_441+1890 others(15): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+18898_441+1890 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(6): Show |
13 | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0006g0003others(10): Show | 13 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+18897_441+1890 others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0208a0002c0002t0002g0039 | 3 | HG03041.hp1 HG03209.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.441+18896_441+1890 others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0161a0001c0001t0002g0162 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.441+18895_441+1890 others(19): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0163a0009c0014t0002g0164 | 2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.441+18894_441+1890 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(10): Show |
1 | a0002c0002t0001g0069 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.441+18893_441+1890 others(21): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(11): Show |
1 | a0002c0002t0001g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.441+18892_441+1890 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(17): Show |
1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441+18909_441+1891 others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(18): Show |
5 | a0001c0001t0001g0090a0002c0002t0001g0012a0002c0002t0001g0061others(2): Show | 5 | HG00735.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+18909_441+1891 others(29): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
A | ATTTTTTT others(19): Show |
1 | a0002c0002t0002g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.441+18909_441+1891 others(30): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153340
|
AT | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0002c0002t0001g0087others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+18909delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | |||||
| chr2:85153381
|
A | G | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+18931A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153381 | ||||||
| chr2:85153514
|
T | G | 8 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0230others(5): Show | 8 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+19064T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153514 | ||||||
| chr2:85153543
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0001g0234a0006c0006t0010g0233 | 3 | HG02723.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.441+19093G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153543 | ||||||
| chr2:85153621
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+19171G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153621 | ||||||
| chr2:85153630
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+19180T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153630 | ||||||
| chr2:85153724
|
A | T | 1 | a0001c0001t0002g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+19274A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153724 | ||||||
| chr2:85153953
|
G | A | 15 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(12): Show | 15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+19503G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153953 | ||||||
| chr2:85154134
|
A | G | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+19684A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154134 | ||||||
| chr2:85154147
|
C | T | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+19697C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154147 | ||||||
| chr2:85154192
|
G | A | 3 | a0001c0001t0002g0167a0001c0001t0002g0174a0001c0001t0002g0175 | 3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+19742G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154192 | ||||||
| chr2:85154293
|
T | C | 11 | a0001c0001t0001g0031a0001c0001t0002g0098a0001c0001t0002g0147others(8): Show | 11 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.441+19843T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154293 | ||||||
| chr2:85154344
|
A | G | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+19894A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154344 | ||||||
| chr2:85154533
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0215a0001c0001t0001g0217 | 3 | HG00280.hp1 HG01358.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.441+20083C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154533 | ||||||
| chr2:85154737
|
C | T | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.441+20287C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154737 | ||||||
| chr2:85154768
|
A | G | 7 | a0001c0001t0001g0088a0002c0002t0001g0089a0002c0002t0002g0016others(4): Show | 7 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+20318A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154768 | ||||||
| chr2:85154823
|
C | CT | 6 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+20386dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85154823 | |||||
| chr2:85154871
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+20421C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154871 | ||||||
| chr2:85154888
|
C | G | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+20438C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154888 | ||||||
| chr2:85154970
|
C | A | 2 | a0001c0001t0007g0114a0005c0005t0001g0115 | 2 | HG01256.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.441+20520C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154970 | ||||||
| chr2:85155009
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.441+20559G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155009 | ||||||
| chr2:85155177
|
C | T | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441+20727C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155177 | ||||||
| chr2:85155236
|
G | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.441+20786G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155236 | ||||||
| chr2:85155291
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+20841A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155291 | ||||||
| chr2:85155297
|
G | A | 1 | a0002c0002t0002g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.441+20847G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155297 | ||||||
| chr2:85155325
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+20875C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155325 | ||||||
| chr2:85155346
|
C | A | 19 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0163others(16): Show | 19 | HG00735.hp1 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.441+20896C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155346 | ||||||
| chr2:85155350
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.441+20900G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155350 | ||||||
| chr2:85155388
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.441+20938A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155388 | ||||||
| chr2:85155607
|
A | T | 120 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0090others(117): Show | 120 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.441+21157A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155607 | ||||||
| chr2:85155910
|
G | T | 1 | a0005c0005t0009g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441+21460G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155910 | ||||||
| chr2:85155911
|
G | T | 1 | a0005c0005t0009g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441+21461G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155911 | ||||||
| chr2:85156002
|
A | T | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+21552A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156002 | ||||||
| chr2:85156015
|
G | A | 2 | a0002c0002t0001g0057a0002c0002t0002g0058 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.441+21565G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156015 | ||||||
| chr2:85156065
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441+21615A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156065 | ||||||
| chr2:85156318
|
T | G | 5 | a0002c0002t0001g0089a0002c0002t0002g0016a0002c0002t0002g0018others(2): Show | 5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+21868T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156318 | ||||||
| chr2:85156562
|
T | C | 2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.441+22112T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156562 | ||||||
| chr2:85156661
|
T | C | 7 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0229others(4): Show | 7 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+22211T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156661 | ||||||
| chr2:85156782
|
C | T | 2 | a0002c0002t0001g0061a0002c0002t0002g0062 | 2 | HG00735.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.441+22332C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156782 | ||||||
| chr2:85156790
|
T | C | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+22340T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156790 | ||||||
| chr2:85156867
|
GATATTTT others(8): Show |
G | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+22447_441+2246 others(19): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85156867 | |||||
| chr2:85157056
|
C | T | 19 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0148others(16): Show | 19 | HG00597.hp1 HG00639.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+22606C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157056 | ||||||
| chr2:85157245
|
G | T | 1 | a0008c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.441+22795G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157245 | ||||||
| chr2:85157264
|
C | A | 1 | a0002c0002t0001g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.441+22814C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157264 | ||||||
| chr2:85157629
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.441+23179A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157629 | ||||||
| chr2:85157830
|
C | A | 2 | a0001c0001t0002g0103a0004c0004t0002g0123 | 2 | HG01346.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.441+23380C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157830 | ||||||
| chr2:85157868
|
C | G | 7 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0040others(4): Show | 7 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+23418C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157868 | ||||||
| chr2:85157893
|
C | T | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+23443C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157893 | ||||||
| chr2:85157929
|
T | C | 28 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0163others(25): Show | 28 | HG00735.hp1 HG01071.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.441+23479T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157929 | ||||||
| chr2:85157994
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+23544G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157994 | ||||||
| chr2:85158272
|
C | T | 1 | a0002c0002t0001g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.441+23822C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158272 | ||||||
| chr2:85158315
|
C | T | 6 | a0001c0001t0001g0092a0001c0001t0005g0001a0001c0001t0005g0002others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+23865C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158315 | ||||||
| chr2:85158345
|
T | A | 5 | a0002c0002t0001g0089a0002c0002t0002g0016a0002c0002t0002g0018others(2): Show | 5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+23895T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158345 | ||||||
| chr2:85158349
|
G | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.441+23899G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158349 | ||||||
| chr2:85158580
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+24130T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158580 | ||||||
| chr2:85158672
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+24222G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158672 | ||||||
| chr2:85158735
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+24285G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158735 | ||||||
| chr2:85159045
|
G | A | 1 | a0004c0004t0002g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.441+24595G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85159045 | ||||||
| chr2:85159638
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+25188A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85159638 | ||||||
| chr2:85160046
|
C | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02257.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+25596C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160046 | ||||||
| chr2:85160347
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+25897C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160347 | ||||||
| chr2:85160370
|
A | G | 133 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(130): Show | 133 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.441+25920A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160370 | ||||||
| chr2:85160382
|
G | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+25932G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160382 | ||||||
| chr2:85160628
|
G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+26178G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160628 | ||||||
| chr2:85160676
|
G | A | 2 | a0003c0003t0002g0086a0005c0012t0002g0184 | 2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.441+26226G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160676 | ||||||
| chr2:85160829
|
G | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+26379G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160829 | ||||||
| chr2:85160901
|
GCA | G | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+26452_441+2645 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160901 | ||||||
| chr2:85160906
|
C | A | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+26456C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160906 | ||||||
| chr2:85160911
|
A | G | 2 | a0001c0001t0002g0100a0002c0002t0002g0017 | 2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+26461A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160911 | ||||||
| chr2:85161061
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441+26611C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161061 | ||||||
| chr2:85161062
|
C | T | 1 | a0002c0002t0001g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.441+26612C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161062 | ||||||
| chr2:85161063
|
G | A | 12 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0196others(9): Show | 12 | HG00621.hp1 HG02080.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+26613G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161063 | ||||||
| chr2:85161134
|
C | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0110a0001c0001t0001g0111others(20): Show | 23 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.441+26684C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161134 | ||||||
| chr2:85161185
|
G | A | 2 | a0001c0001t0001g0121a0002c0002t0003g0083 | 2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.441+26735G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161185 | ||||||
| chr2:85161221
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441+26771A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161221 | ||||||
| chr2:85161233
|
A | G | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+26783A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161233 | ||||||
| chr2:85161359
|
G | C | 1 | a0001c0001t0007g0114 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.441+26909G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161359 | ||||||
| chr2:85161444
|
G | T | 1 | a0001c0001t0002g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.441+26994G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161444 | ||||||
| chr2:85161625
|
C | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0110a0001c0001t0001g0111others(19): Show | 22 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.441+27175C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161625 | ||||||
| chr2:85161870
|
C | T | 11 | a0001c0001t0001g0160a0001c0001t0001g0206a0001c0001t0001g0224others(8): Show | 11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+27420C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161870 | ||||||
| chr2:85161891
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+27441C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161891 | ||||||
| chr2:85161907
|
G | C | 2 | a0001c0001t0001g0121a0002c0002t0003g0083 | 2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.441+27457G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161907 | ||||||
| chr2:85162045
|
A | G | 36 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(33): Show | 36 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+27595A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162045 | ||||||
| chr2:85162057
|
T | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+27607T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162057 | ||||||
| chr2:85162062
|
A | G | 11 | a0001c0001t0001g0160a0001c0001t0001g0206a0001c0001t0001g0224others(8): Show | 11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+27612A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162062 | ||||||
| chr2:85162073
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.441+27623A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162073 | ||||||
| chr2:85162111
|
T | C | 2 | a0001c0001t0002g0100a0002c0002t0002g0017 | 2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+27661T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162111 | ||||||
| chr2:85162174
|
G | T | 1 | a0001c0001t0006g0005 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.441+27724G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162174 | ||||||
| chr2:85162182
|
G | C | 34 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(31): Show | 34 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+27732G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162182 | ||||||
| chr2:85162282
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441+27832C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162282 | ||||||
| chr2:85162489
|
C | T | 2 | a0002c0002t0001g0093a0002c0002t0001g0094 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.441+28039C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162489 | ||||||
| chr2:85162562
|
T | C | 36 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(33): Show | 36 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+28112T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162562 | ||||||
| chr2:85162568
|
A | G | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+28118A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162568 | ||||||
| chr2:85162572
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.441+28122T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162572 | ||||||
| chr2:85162582
|
C | T | 11 | a0001c0001t0001g0160a0001c0001t0001g0206a0001c0001t0001g0224others(8): Show | 11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+28132C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162582 | ||||||
| chr2:85162591
|
T | A | 11 | a0001c0001t0001g0160a0001c0001t0001g0206a0001c0001t0001g0224others(8): Show | 11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+28141T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162591 | ||||||
| chr2:85162653
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.441+28203C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162653 | ||||||
| chr2:85162667
|
G | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+28217G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162667 | ||||||
| chr2:85162717
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+28267C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162717 | ||||||
| chr2:85162852
|
T | C | 34 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(31): Show | 34 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+28402T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162852 | ||||||
| chr2:85162918
|
C | A | 39 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(36): Show | 39 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.441+28468C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162918 | ||||||
| chr2:85162963
|
A | C | 2 | a0001c0001t0001g0206a0001c0001t0002g0205 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.441+28513A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162963 | ||||||
| chr2:85163042
|
G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+28592G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163042 | ||||||
| chr2:85163080
|
G | A | 1 | a0003c0003t0002g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441+28630G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163080 | ||||||
| chr2:85163318
|
C | A | 14 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0140others(11): Show | 14 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+28868C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163318 | ||||||
| chr2:85163631
|
G | C | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+29181G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163631 | ||||||
| chr2:85163659
|
G | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+29209G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163659 | ||||||
| chr2:85163709
|
G | A | 2 | a0001c0001t0002g0100a0002c0002t0002g0017 | 2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+29259G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163709 | ||||||
| chr2:85163774
|
TA | T | 2 | a0002c0007t0002g0029a0003c0003t0002g0036 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.441+29325delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163774 | ||||||
| chr2:85163952
|
T | C | 1 | a0002c0002t0003g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.441+29502T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163952 | ||||||
| chr2:85164132
|
C | T | 46 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0096others(43): Show | 46 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.441+29682C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164132 | ||||||
| chr2:85164163
|
C | T | 2 | a0001c0001t0001g0219a0011c0017t0001g0220 | 2 | HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.441+29713C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164163 | ||||||
| chr2:85164185
|
G | A | 39 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(36): Show | 39 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.441+29735G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164185 | ||||||
| chr2:85164252
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0002g0141a0002c0002t0001g0093others(2): Show | 5 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+29802G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164252 | ||||||
| chr2:85164344
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.441+29894G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164344 | ||||||
| chr2:85164441
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+29991G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164441 | ||||||
| chr2:85164622
|
A | T | 12 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0206others(9): Show | 12 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+30172A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164622 | ||||||
| chr2:85164752
|
G | A | 37 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(34): Show | 37 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.441+30302G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164752 | ||||||
| chr2:85164886
|
T | C | 41 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(38): Show | 41 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.441+30436T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164886 | ||||||
| chr2:85164970
|
A | T | 154 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0091others(151): Show | 154 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.441+30520A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164970 | ||||||
| chr2:85164988
|
T | C | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+30538T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164988 | ||||||
| chr2:85165032
|
A | C | 4 | a0001c0001t0001g0031a0002c0002t0001g0030a0002c0002t0001g0032others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+30582A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165032 | ||||||
| chr2:85165036
|
G | C | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0007g0114others(1): Show | 4 | HG01256.hp1 HG02165.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+30586G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165036 | ||||||
| chr2:85165076
|
C | T | 31 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0110others(28): Show | 31 | HG01175.hp2 HG01243.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+30626C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165076 | ||||||
| chr2:85165093
|
T | G | 79 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0092others(76): Show | 79 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.441+30643T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165093 | ||||||
| chr2:85165362
|
AACAAGC | A | 30 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0133others(27): Show | 30 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+30913_441+3091 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165362 | ||||||
| chr2:85165369
|
C | T | 30 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0133others(27): Show | 30 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+30919C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165369 | ||||||
| chr2:85165371
|
A | T | 30 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0133others(27): Show | 30 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+30921A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165371 | ||||||
| chr2:85165424
|
T | C | 10 | a0001c0001t0001g0092a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+30974T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165424 | ||||||
| chr2:85165852
|
A | G | 12 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0206others(9): Show | 12 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+31402A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165852 | ||||||
| chr2:85165882
|
A | G | 14 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+31432A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165882 | ||||||
| chr2:85165972
|
T | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.441+31522T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165972 | ||||||
| chr2:85166027
|
T | G | 1 | a0002c0002t0001g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.441+31577T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166027 | ||||||
| chr2:85166069
|
G | A | 1 | a0002c0002t0002g0027 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.441+31619G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166069 | ||||||
| chr2:85166541
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441+32091G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166541 | ||||||
| chr2:85166564
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+32114C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166564 | ||||||
| chr2:85166638
|
A | G | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+32188A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166638 | ||||||
| chr2:85166668
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+32218C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166668 | ||||||
| chr2:85166861
|
G | C | 12 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0206others(9): Show | 12 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+32411G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166861 | ||||||
| chr2:85166869
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441+32419T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166869 | ||||||
| chr2:85166882
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+32432C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166882 | ||||||
| chr2:85166959
|
C | T | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0166others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+32509C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166959 | ||||||
| chr2:85166988
|
T | C | 4 | a0001c0001t0001g0092a0001c0001t0002g0141a0002c0002t0001g0093others(1): Show | 4 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+32538T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166988 | ||||||
| chr2:85166991
|
T | C | 89 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(86): Show | 89 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.441+32541T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166991 | ||||||
| chr2:85167023
|
C | T | 11 | a0001c0001t0001g0076a0001c0001t0001g0183a0001c0001t0001g0219others(8): Show | 11 | HG00280.hp2 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+32573C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167023 | ||||||
| chr2:85167139
|
T | G | 18 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(15): Show | 18 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+32689T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167139 | ||||||
| chr2:85167168
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0217a0002c0002t0001g0026 | 3 | HG00280.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.441+32718C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167168 | ||||||
| chr2:85167319
|
A | G | 13 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+32869A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167319 | ||||||
| chr2:85167351
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.441+32901T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167351 | ||||||
| chr2:85167414
|
T | A | 2 | a0001c0001t0001g0128a0002c0002t0001g0025 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.441+32964T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167414 | ||||||
| chr2:85167449
|
C | G | 27 | a0001c0001t0001g0092a0001c0001t0001g0145a0001c0001t0001g0160others(24): Show | 27 | HG00735.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.441+32999C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167449 | ||||||
| chr2:85167488
|
A | G | 67 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(64): Show | 67 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.441+33038A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167488 | ||||||
| chr2:85167506
|
C | T | 1 | a0010c0015t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441+33056C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167506 | ||||||
| chr2:85167981
|
C | T | 49 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(46): Show | 49 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.441+33531C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167981 | ||||||
| chr2:85168047
|
A | G | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33597A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168047 | ||||||
| chr2:85168068
|
TAA | T | 16 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(13): Show | 16 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+33620_441+3362 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168068 | |||||
| chr2:85168082
|
T | A | 1 | a0001c0001t0006g0005 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.441+33632T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168082 | ||||||
| chr2:85168192
|
A | AAC | 18 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(15): Show | 18 | HG01515.hp1 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+33772_441+3377 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACAC | 5 | a0001c0001t0001g0031a0001c0001t0002g0098a0002c0002t0001g0032others(2): Show | 5 | HG02818.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+33770_441+3377 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACAC | 8 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0002g0141others(5): Show | 8 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+33768_441+3377 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACACA others(1): Show |
7 | a0001c0001t0001g0088a0001c0001t0001g0117a0001c0001t0002g0157others(4): Show | 7 | HG00639.hp1 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+33766_441+3377 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACACA others(3): Show |
17 | a0001c0001t0001g0128a0001c0001t0001g0160a0001c0001t0001g0200others(14): Show | 17 | HG01168.hp1 HG01934.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.441+33764_441+3377 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACACA others(5): Show |
20 | a0001c0001t0001g0095a0001c0001t0001g0105a0001c0001t0001g0107others(17): Show | 20 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.441+33762_441+3377 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACACA others(7): Show |
10 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0196others(7): Show | 10 | HG01358.hp1 HG02572.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+33760_441+3377 others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACACA others(9): Show |
2 | a0002c0007t0002g0029a0006c0006t0002g0108 | 2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.441+33758_441+3377 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACACA others(11): Show |
8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+33756_441+3377 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
A | AACACACA others(17): Show |
1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+33750_441+3377 others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168192
|
AACAC | A | 15 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(12): Show | 15 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+33770_441+3377 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | |||||
| chr2:85168224
|
A | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+33774A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168224 | ||||||
| chr2:85168234
|
A | T | 74 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(71): Show | 74 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.441+33784A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168234 | ||||||
| chr2:85168378
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33928G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168378 | ||||||
| chr2:85168409
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33959C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168409 | ||||||
| chr2:85168420
|
G | A | 2 | a0001c0001t0002g0100a0002c0007t0002g0029 | 2 | HG02647.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+33970G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168420 | ||||||
| chr2:85168421
|
A | C | 2 | a0001c0001t0002g0100a0002c0007t0002g0029 | 2 | HG02647.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+33971A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168421 | ||||||
| chr2:85168434
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33984G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168434 | ||||||
| chr2:85168457
|
C | G | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+34007C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168457 | ||||||
| chr2:85168488
|
G | A | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+34038G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168488 | ||||||
| chr2:85168503
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+34053G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168503 | ||||||
| chr2:85168613
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.441+34163T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168613 | ||||||
| chr2:85168626
|
CT | C | 5 | a0001c0001t0001g0088a0001c0001t0001g0225a0001c0001t0002g0157others(2): Show | 5 | HG00741.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+34189delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168626 | |||||
| chr2:85168672
|
A | C | 1 | a0001c0001t0002g0189 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.441+34222A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168672 | ||||||
| chr2:85168714
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+34264C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168714 | ||||||
| chr2:85168783
|
G | A | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+34333G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168783 | ||||||
| chr2:85168823
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+34373A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168823 | ||||||
| chr2:85168935
|
G | T | 15 | a0001c0001t0001g0160a0001c0001t0001g0206a0001c0001t0001g0210others(12): Show | 15 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+34485G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168935 | ||||||
| chr2:85168956
|
G | A | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+34506G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168956 | ||||||
| chr2:85169024
|
A | G | 6 | a0001c0001t0001g0092a0001c0001t0002g0141a0001c0001t0002g0214others(3): Show | 6 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+34574A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169024 | ||||||
| chr2:85169144
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0002g0141a0002c0002t0001g0093others(2): Show | 5 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+34694G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169144 | ||||||
| chr2:85169174
|
C | G | 16 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(13): Show | 16 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+34724C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169174 | ||||||
| chr2:85169284
|
C | A | 40 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(37): Show | 40 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.441+34834C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169284 | ||||||
| chr2:85169284
|
C | G | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+34834C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169284 | ||||||
| chr2:85169366
|
T | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+34916T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169366 | ||||||
| chr2:85169504
|
T | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35054T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169504 | ||||||
| chr2:85169517
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35067A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169517 | ||||||
| chr2:85169579
|
A | G | 13 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+35129A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169579 | ||||||
| chr2:85169770
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35320A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169770 | ||||||
| chr2:85169819
|
G | A | 4 | a0001c0001t0001g0088a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+35369G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169819 | ||||||
| chr2:85169836
|
G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35386G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169836 | ||||||
| chr2:85169884
|
C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35434C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169884 | ||||||
| chr2:85170315
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+35865C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170315 | ||||||
| chr2:85170592
|
G | A | 1 | a0010c0015t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441+36142G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170592 | ||||||
| chr2:85170631
|
T | G | 1 | a0001c0001t0002g0187 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.441+36181T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170631 | ||||||
| chr2:85170877
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+36427G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170877 | ||||||
| chr2:85170934
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+36484C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170934 | ||||||
| chr2:85171038
|
G | GA | 4 | a0001c0001t0001g0088a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+36595dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85171038 | |||||
| chr2:85171080
|
G | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+36630G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171080 | ||||||
| chr2:85171124
|
A | G | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+36674A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171124 | ||||||
| chr2:85171154
|
G | A | 6 | a0001c0001t0001g0092a0001c0001t0002g0098a0001c0001t0002g0141others(3): Show | 6 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+36704G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171154 | ||||||
| chr2:85171204
|
C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+36754C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171204 | ||||||
| chr2:85171588
|
A | G | 1 | a0002c0002t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.441+37138A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171588 | ||||||
| chr2:85171847
|
C | T | 1 | a0002c0002t0001g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.441+37397C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171847 | ||||||
| chr2:85171928
|
C | T | 1 | a0002c0002t0002g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.441+37478C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171928 | ||||||
| chr2:85172039
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0137 | 2 | NA18961.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.441+37589A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172039 | ||||||
| chr2:85172172
|
A | G | 2 | a0001c0001t0002g0100a0004c0004t0002g0124 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+37722A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172172 | ||||||
| chr2:85172173
|
C | T | 82 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0092others(79): Show | 82 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.441+37723C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172173 | ||||||
| chr2:85172193
|
C | A | 12 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0140others(9): Show | 12 | HG00597.hp2 HG00639.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+37743C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172193 | ||||||
| chr2:85172209
|
A | G | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+37759A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172209 | ||||||
| chr2:85172244
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0002g0141a0001c0001t0002g0157others(4): Show | 7 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+37794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172244 | ||||||
| chr2:85172245
|
G | A | 2 | a0001c0001t0002g0100a0004c0004t0002g0124 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+37795G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172245 | ||||||
| chr2:85172284
|
A | C | 2 | a0001c0001t0001g0107a0006c0006t0002g0108 | 2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.441+37834A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172284 | ||||||
| chr2:85172457
|
C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+38007C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172457 | ||||||
| chr2:85172632
|
G | A | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38182G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172632 | ||||||
| chr2:85172701
|
T | C | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172701 | ||||||
| chr2:85172715
|
C | A | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38265C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172715 | ||||||
| chr2:85172768
|
C | T | 2 | a0002c0002t0002g0016a0002c0002t0012g0021 | 2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.441+38318C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172768 | ||||||
| chr2:85172783
|
C | G | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38333C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172783 | ||||||
| chr2:85172902
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.441+38452C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172902 | ||||||
| chr2:85172929
|
G | A | 1 | a0008c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.441+38479G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172929 | ||||||
| chr2:85172939
|
G | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.441+38489G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172939 | ||||||
| chr2:85172974
|
G | A | 2 | a0002c0002t0001g0093a0002c0002t0001g0094 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.441+38524G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172974 | ||||||
| chr2:85173038
|
C | T | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+38588C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173038 | ||||||
| chr2:85173091
|
C | G | 1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.441+38641C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173091 | ||||||
| chr2:85173113
|
G | T | 1 | a0001c0001t0002g0189 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.441+38663G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173113 | ||||||
| chr2:85173136
|
A | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+38686A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173136 | ||||||
| chr2:85173446
|
T | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+38996T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173446 | ||||||
| chr2:85173449
|
G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+38999G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173449 | ||||||
| chr2:85173461
|
C | T | 41 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0133others(38): Show | 41 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.441+39011C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173461 | ||||||
| chr2:85173462
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+39012G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173462 | ||||||
| chr2:85173479
|
G | C | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+39029G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173479 | ||||||
| chr2:85173574
|
C | A | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+39124C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173574 | ||||||
| chr2:85173605
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.441+39155C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173605 | ||||||
| chr2:85173626
|
G | T | 1 | a0002c0002t0004g0055 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.441+39176G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173626 | ||||||
| chr2:85173677
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+39227G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173677 | ||||||
| chr2:85173678
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+39228G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173678 | ||||||
| chr2:85173743
|
C | CT | 50 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(47): Show | 50 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.441+39302dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173743 | |||||
| chr2:85173753
|
C | CTTTCTTT others(13): Show |
1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+39304_441+3930 others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173753 | |||||
| chr2:85173753
|
C | CTTTCTTT others(15): Show |
3 | a0001c0001t0001g0210a0003c0003t0002g0086a0005c0012t0002g0184 | 3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+39304_441+3930 others(26): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173753 | |||||
| chr2:85173753
|
C | CTTTCTTT others(16): Show |
1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441+39304_441+3930 others(27): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173753 | |||||
| chr2:85173797
|
C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+39347C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173797 | ||||||
| chr2:85173839
|
C | G | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+39389C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173839 | ||||||
| chr2:85173854
|
G | A | 28 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(25): Show | 28 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.441+39404G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173854 | ||||||
| chr2:85173893
|
C | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+39443C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173893 | ||||||
| chr2:85173977
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+39527C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173977 | ||||||
| chr2:85173982
|
G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+39532G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173982 | ||||||
| chr2:85174215
|
T | C | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+39765T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174215 | ||||||
| chr2:85174228
|
G | A | 4 | a0001c0001t0001g0107a0002c0002t0001g0034a0002c0002t0002g0018others(1): Show | 4 | HG03209.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+39778G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174228 | ||||||
| chr2:85174465
|
G | A | 1 | a0002c0002t0001g0038 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.441+40015G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174465 | ||||||
| chr2:85174483
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+40033A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174483 | ||||||
| chr2:85174486
|
T | A | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+40036T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174486 | ||||||
| chr2:85174541
|
A | G | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40091A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174541 | ||||||
| chr2:85174631
|
T | C | 10 | a0001c0001t0001g0149a0001c0001t0001g0188a0001c0001t0001g0190others(7): Show | 10 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+40181T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174631 | ||||||
| chr2:85174722
|
A | G | 5 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0105others(2): Show | 5 | HG00597.hp1 NA18959.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40272A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174722 | ||||||
| chr2:85174755
|
A | G | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40305A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174755 | ||||||
| chr2:85174768
|
G | A | 1 | a0001c0001t0011g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.441+40318G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174768 | ||||||
| chr2:85174835
|
C | T | 141 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(138): Show | 141 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.441+40385C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174835 | ||||||
| chr2:85174932
|
G | A | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+40482G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174932 | ||||||
| chr2:85174983
|
G | A | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40533G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174983 | ||||||
| chr2:85174990
|
G | A | 6 | a0002c0002t0001g0038a0002c0002t0001g0040a0002c0002t0001g0042others(3): Show | 6 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+40540G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174990 | ||||||
| chr2:85175056
|
C | T | 12 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+40606C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175056 | ||||||
| chr2:85175213
|
C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+40763C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175213 | ||||||
| chr2:85175370
|
C | T | 11 | a0001c0001t0001g0122a0001c0001t0001g0160a0001c0001t0001g0206others(8): Show | 11 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+40920C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175370 | ||||||
| chr2:85175521
|
G | T | 3 | a0002c0002t0001g0035a0002c0002t0003g0073a0002c0002t0003g0074 | 3 | HG01106.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.441+41071G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175521 | ||||||
| chr2:85175691
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+41241T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175691 | ||||||
| chr2:85175744
|
G | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+41294G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175744 | ||||||
| chr2:85175851
|
A | C | 77 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(74): Show | 77 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.441+41401A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175851 | ||||||
| chr2:85175927
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.441+41477G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175927 | ||||||
| chr2:85176027
|
A | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.441+41577A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176027 | ||||||
| chr2:85176118
|
T | C | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+41668T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176118 | ||||||
| chr2:85176225
|
C | G | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+41775C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176225 | ||||||
| chr2:85176423
|
A | G | 39 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(36): Show | 39 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.441+41973A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176423 | ||||||
| chr2:85176476
|
C | T | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+42026C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176476 | ||||||
| chr2:85176510
|
G | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+42060G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176510 | ||||||
| chr2:85176760
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+42310G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176760 | ||||||
| chr2:85176913
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+42463G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176913 | ||||||
| chr2:85176922
|
G | A | 14 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+42472G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176922 | ||||||
| chr2:85176962
|
G | C | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+42512G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176962 | ||||||
| chr2:85176986
|
C | CA | 50 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0076others(47): Show | 50 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.441+42559dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85176986 | |||||
| chr2:85176986
|
C | CAA | 11 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0135others(8): Show | 11 | HG00597.hp2 HG01981.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+42558_441+4255 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85176986 | |||||
| chr2:85176986
|
CAAAAAAA | C | 12 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+42553_441+4255 others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85176986 | |||||
| chr2:85177244
|
C | T | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+42794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177244 | ||||||
| chr2:85177499
|
A | G | 218 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(215): Show |
intron_variant | MODIFIER | c.441+43049A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177499 | ||||||
| chr2:85177566
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.441+43116G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177566 | ||||||
| chr2:85177661
|
C | T | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+43211C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177661 | ||||||
| chr2:85177760
|
C | G | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+43310C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177760 | ||||||
| chr2:85177814
|
A | G | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+43364A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177814 | ||||||
| chr2:85177909
|
A | G | 75 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(72): Show | 75 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.441+43459A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177909 | ||||||
| chr2:85178129
|
C | T | 3 | a0001c0001t0001g0128a0002c0002t0001g0009a0013c0009t0001g0019 | 3 | HG02895.hp2 HG03195.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.441+43679C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85178129 | ||||||
| chr2:85178139
|
G | A | 4 | a0001c0001t0001g0092a0001c0001t0002g0141a0002c0002t0001g0093others(1): Show | 4 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+43689G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85178139 | ||||||
| chr2:85178246
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.441+43796G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85178246 | ||||||
| chr2:85179000
|
G | A | 1 | a0004c0004t0002g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.441+44550G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179000 | ||||||
| chr2:85179103
|
G | A | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+44653G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179103 | ||||||
| chr2:85179201
|
G | A | 2 | a0002c0002t0001g0009a0013c0009t0001g0019 | 2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.441+44751G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179201 | ||||||
| chr2:85179445
|
T | C | 1 | a0005c0012t0002g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.441+44995T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179445 | ||||||
| chr2:85179495
|
T | C | 14 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+45045T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179495 | ||||||
| chr2:85179496
|
C | T | 14 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+45046C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179496 | ||||||
| chr2:85179726
|
C | T | 5 | a0001c0001t0001g0210a0002c0002t0002g0017a0002c0007t0002g0029others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+45276C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179726 | ||||||
| chr2:85179737
|
C | CT | 15 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(12): Show | 15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+45288dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85179737 | |||||
| chr2:85179753
|
T | A | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+45303T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179753 | ||||||
| chr2:85180047
|
G | A | 4 | a0001c0001t0001g0232a0001c0001t0002g0067a0002c0002t0002g0016others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+45597G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180047 | ||||||
| chr2:85180216
|
T | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+45766T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180216 | ||||||
| chr2:85180222
|
G | T | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+45772G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180222 | ||||||
| chr2:85180224
|
T | G | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+45774T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180224 | ||||||
| chr2:85180234
|
G | GT | 14 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+45795dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85180234 | |||||
| chr2:85180240
|
T | G | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+45790T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180240 | ||||||
| chr2:85180366
|
C | T | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+45916C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180366 | ||||||
| chr2:85180447
|
G | A | 12 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(9): Show | 12 | HG01934.hp2 HG02056.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+45997G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180447 | ||||||
| chr2:85180549
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.441+46099A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180549 | ||||||
| chr2:85180577
|
A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.441+46127A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180577 | ||||||
| chr2:85180775
|
C | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441+46325C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180775 | ||||||
| chr2:85180897
|
C | T | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+46447C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180897 | ||||||
| chr2:85180961
|
G | A | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+46511G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180961 | ||||||
| chr2:85181114
|
T | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+46664T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181114 | ||||||
| chr2:85181175
|
G | A | 24 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(21): Show | 24 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+46725G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181175 | ||||||
| chr2:85181241
|
G | A | 18 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(15): Show | 18 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+46791G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181241 | ||||||
| chr2:85181245
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.441+46795G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181245 | ||||||
| chr2:85181361
|
C | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+46911C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181361 | ||||||
| chr2:85181384
|
A | G | 3 | a0001c0001t0001g0210a0003c0003t0002g0086a0005c0012t0002g0184 | 3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+46934A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181384 | ||||||
| chr2:85181428
|
A | G | 93 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(90): Show | 93 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.441+46978A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181428 | ||||||
| chr2:85181700
|
G | A | 1 | a0002c0002t0003g0176 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.441+47250G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181700 | ||||||
| chr2:85181843
|
G | A | 24 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(21): Show | 24 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+47393G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181843 | ||||||
| chr2:85181937
|
T | C | 15 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(12): Show | 15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+47487T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181937 | ||||||
| chr2:85182109
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.441+47659G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182109 | ||||||
| chr2:85182116
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.441+47666G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182116 | ||||||
| chr2:85182177
|
G | A | 14 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(11): Show | 14 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+47727G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182177 | ||||||
| chr2:85182236
|
C | T | 15 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(12): Show | 15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+47786C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182236 | ||||||
| chr2:85182319
|
G | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0097a0001c0001t0001g0129others(4): Show | 7 | HG00621.hp2 HG02165.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+47869G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182319 | ||||||
| chr2:85182388
|
G | A | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+47938G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182388 | ||||||
| chr2:85182446
|
C | T | 2 | a0001c0001t0001g0121a0002c0002t0003g0083 | 2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.441+47996C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182446 | ||||||
| chr2:85182498
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.441+48048G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182498 | ||||||
| chr2:85182867
|
A | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+48417A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182867 | ||||||
| chr2:85182966
|
G | A | 89 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(86): Show | 89 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.441+48516G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182966 | ||||||
| chr2:85182981
|
G | A | 37 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(34): Show | 37 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.441+48531G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182981 | ||||||
| chr2:85183400
|
C | G | 2 | a0001c0001t0001g0091a0001c0001t0011g0116 | 2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.441+48950C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183400 | ||||||
| chr2:85183444
|
T | C | 1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.441+48994T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183444 | ||||||
| chr2:85183509
|
C | T | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+49059C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183509 | ||||||
| chr2:85183714
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.441+49264G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183714 | ||||||
| chr2:85183747
|
G | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0137a0001c0001t0002g0136others(1): Show | 4 | HG02165.hp1 NA18961.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+49297G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183747 | ||||||
| chr2:85183810
|
C | T | 27 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(24): Show | 27 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.441+49360C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183810 | ||||||
| chr2:85184047
|
G | A | 1 | a0005c0005t0009g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441+49597G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184047 | ||||||
| chr2:85184276
|
C | T | 15 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(12): Show | 15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+49826C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184276 | ||||||
| chr2:85184380
|
G | A | 7 | a0001c0001t0001g0132a0001c0001t0001g0151a0001c0001t0002g0134others(4): Show | 7 | HG00741.hp1 HG01109.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+49930G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184380 | ||||||
| chr2:85184445
|
T | C | 13 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+49995T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184445 | ||||||
| chr2:85184461
|
G | A | 12 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+50011G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184461 | ||||||
| chr2:85184675
|
G | A | 12 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(9): Show | 12 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+50225G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184675 | ||||||
| chr2:85184759
|
T | TGGTATAG others(58): Show |
1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.441+50313_441+5037 others(69): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85184759 | |||||
| chr2:85184761
|
G | A | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+50311G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184761 | ||||||
| chr2:85185006
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+50556T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185006 | ||||||
| chr2:85185029
|
G | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+50579G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185029 | ||||||
| chr2:85185196
|
C | G | 1 | a0001c0001t0002g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.441+50746C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185196 | ||||||
| chr2:85185286
|
G | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+50836G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185286 | ||||||
| chr2:85185298
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+50848C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185298 | ||||||
| chr2:85185528
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.441+51078G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185528 | ||||||
| chr2:85185622
|
C | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+51172C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185622 | ||||||
| chr2:85185653
|
T | C | 36 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(33): Show | 36 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.441+51203T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185653 | ||||||
| chr2:85185711
|
T | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+51261T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185711 | ||||||
| chr2:85185823
|
G | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+51373G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185823 | ||||||
| chr2:85185945
|
G | A | 104 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(101): Show | 104 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.441+51495G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185945 | ||||||
| chr2:85185958
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.441+51508G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185958 | ||||||
| chr2:85185959
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.441+51509G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185959 | ||||||
| chr2:85185960
|
A | AT | 48 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0088others(45): Show | 48 | HG00597.hp1 HG01109.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.441+51534dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85185960 | |||||
| chr2:85185960
|
A | ATT | 29 | a0001c0001t0001g0112a0001c0001t0001g0149a0001c0001t0001g0161others(26): Show | 29 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.441+51533_441+5153 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85185960 | |||||
| chr2:85185960
|
AT | A | 29 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0135others(26): Show | 29 | HG00735.hp1 HG01106.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.441+51534delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85185960 | |||||
| chr2:85186052
|
T | C | 54 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(51): Show | 54 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.441+51602T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186052 | ||||||
| chr2:85186300
|
A | G | 3 | a0001c0001t0002g0202a0002c0002t0001g0037a0002c0002t0003g0084 | 3 | HG02809.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.441+51850A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186300 | ||||||
| chr2:85186443
|
C | CT | 51 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(48): Show | 51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.441+51993_441+5199 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186443 | ||||||
| chr2:85186540
|
T | C | 113 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(110): Show | 113 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.441+52090T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186540 | ||||||
| chr2:85186775
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+52325T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186775 | ||||||
| chr2:85186849
|
T | C | 38 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(35): Show | 38 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.441+52399T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186849 | ||||||
| chr2:85186893
|
A | C | 38 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(35): Show | 38 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.441+52443A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186893 | ||||||
| chr2:85187017
|
G | A | 155 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(152): Show | 155 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.441+52567G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187017 | ||||||
| chr2:85187197
|
A | C | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+52747A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187197 | ||||||
| chr2:85187198
|
G | C | 2 | a0002c0002t0001g0093a0002c0002t0001g0094 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.441+52748G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187198 | ||||||
| chr2:85187214
|
G | T | 1 | a0002c0002t0002g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.441+52764G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187214 | ||||||
| chr2:85187333
|
A | C | 2 | a0001c0001t0001g0179a0002c0002t0003g0078 | 2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.441+52883A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187333 | ||||||
| chr2:85187524
|
G | A | 50 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(47): Show | 50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.441+53074G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187524 | ||||||
| chr2:85187714
|
C | G | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+53264C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187714 | ||||||
| chr2:85187730
|
A | G | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+53280A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187730 | ||||||
| chr2:85187811
|
T | C | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+53361T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187811 | ||||||
| chr2:85187843
|
C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+53393C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187843 | ||||||
| chr2:85187894
|
T | C | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+53444T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187894 | ||||||
| chr2:85188115
|
C | T | 1 | a0004c0004t0002g0142 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.441+53665C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188115 | ||||||
| chr2:85188306
|
A | T | 149 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(146): Show | 149 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.441+53856A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188306 | ||||||
| chr2:85188312
|
C | A | 8 | a0001c0001t0001g0092a0001c0001t0001g0232a0001c0001t0002g0067others(5): Show | 8 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+53862C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188312 | ||||||
| chr2:85188345
|
T | C | 2 | a0002c0002t0001g0009a0013c0009t0001g0019 | 2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.441+53895T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188345 | ||||||
| chr2:85188350
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+53900G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188350 | ||||||
| chr2:85188369
|
A | C | 3 | a0001c0001t0002g0167a0001c0001t0002g0174a0001c0001t0002g0175 | 3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+53919A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188369 | ||||||
| chr2:85188423
|
T | C | 2 | a0001c0001t0001g0179a0002c0002t0003g0078 | 2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.441+53973T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188423 | ||||||
| chr2:85188680
|
C | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+54230C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188680 | ||||||
| chr2:85188691
|
G | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+54241G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188691 | ||||||
| chr2:85188815
|
CT | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+54367delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85188815 | |||||
| chr2:85188966
|
T | A | 2 | a0002c0002t0001g0009a0013c0009t0001g0019 | 2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.441+54516T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188966 | ||||||
| chr2:85189170
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.441+54720T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189170 | ||||||
| chr2:85189173
|
C | G | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0210others(7): Show | 10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+54723C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189173 | ||||||
| chr2:85189285
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.441+54835G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189285 | ||||||
| chr2:85189391
|
A | G | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+54941A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189391 | ||||||
| chr2:85189579
|
C | G | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+55129C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189579 | ||||||
| chr2:85189831
|
A | G | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+55381A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189831 | ||||||
| chr2:85189990
|
G | A | 1 | a0001c0001t0011g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.441+55540G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189990 | ||||||
| chr2:85190119
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.441+55669C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85190119 | ||||||
| chr2:85190352
|
C | T | 6 | a0001c0001t0001g0088a0001c0001t0002g0157a0001c0001t0002g0158others(3): Show | 6 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+55902C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85190352 | ||||||
| chr2:85191586
|
G | A | 1 | a0002c0002t0002g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.441+57136G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191586 | ||||||
| chr2:85191711
|
G | C | 8 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(5): Show | 8 | HG02572.hp2 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+57261G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191711 | ||||||
| chr2:85191718
|
G | C | 13 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+57268G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191718 | ||||||
| chr2:85191740
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.441+57290G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191740 | ||||||
| chr2:85191783
|
T | C | 85 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(82): Show | 85 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.441+57333T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191783 | ||||||
| chr2:85191825
|
C | CA | 20 | a0001c0001t0001g0090a0001c0001t0001g0144a0001c0001t0001g0161others(17): Show | 20 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.441+57391dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85191825 | |||||
| chr2:85191847
|
T | C | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+57397T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191847 | ||||||
| chr2:85191901
|
A | T | 1 | a0002c0002t0003g0176 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.441+57451A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191901 | ||||||
| chr2:85192053
|
T | C | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441+57603T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192053 | ||||||
| chr2:85192287
|
CT | C | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+57838delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192287 | ||||||
| chr2:85192375
|
G | T | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+57925G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192375 | ||||||
| chr2:85192398
|
T | A | 27 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0163others(24): Show | 27 | HG00735.hp1 HG02109.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.441+57948T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192398 | ||||||
| chr2:85192401
|
T | A | 50 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(47): Show | 50 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.441+57951T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192401 | ||||||
| chr2:85192498
|
A | G | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.441+58048A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192498 | ||||||
| chr2:85192524
|
A | AT | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+58076dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192524 | |||||
| chr2:85192641
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.441+58191C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192641 | ||||||
| chr2:85192661
|
G | T | 32 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+58211G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192661 | ||||||
| chr2:85192663
|
G | T | 20 | a0001c0001t0001g0090a0001c0001t0001g0234a0001c0001t0002g0202others(17): Show | 20 | HG00735.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.441+58213G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192663 | ||||||
| chr2:85192691
|
C | CT | 23 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(20): Show | 23 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.441+58258dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192691 | |||||
| chr2:85192691
|
C | CTT | 8 | a0001c0001t0001g0210a0001c0001t0002g0098a0001c0001t0002g0194others(5): Show | 8 | HG02258.hp1 HG02572.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+58257_441+5825 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192691 | |||||
| chr2:85192691
|
CT | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0137a0001c0001t0001g0234others(7): Show | 10 | HG00735.hp1 HG01167.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+58258delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192691 | |||||
| chr2:85192777
|
T | C | 218 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(215): Show | 218 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(215): Show |
intron_variant | MODIFIER | c.441+58327T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192777 | ||||||
| chr2:85193001
|
C | T | 89 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(86): Show | 89 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.441+58551C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193001 | ||||||
| chr2:85193058
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+58608G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193058 | ||||||
| chr2:85193080
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.441+58630T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193080 | ||||||
| chr2:85193238
|
G | A | 1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441+58788G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193238 | ||||||
| chr2:85193359
|
A | G | 139 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(136): Show | 139 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.441+58909A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193359 | ||||||
| chr2:85193399
|
T | C | 2 | a0001c0001t0001g0179a0002c0002t0003g0078 | 2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.441+58949T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193399 | ||||||
| chr2:85193407
|
G | A | 49 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(46): Show | 49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+58957G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193407 | ||||||
| chr2:85193579
|
T | C | 23 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(20): Show | 23 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.441+59129T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193579 | ||||||
| chr2:85193747
|
T | C | 60 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(57): Show | 60 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.441+59297T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193747 | ||||||
| chr2:85193821
|
G | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+59371G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193821 | ||||||
| chr2:85193894
|
T | G | 19 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(16): Show | 19 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+59444T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193894 | ||||||
| chr2:85193968
|
TA | T | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+59529delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85193968 | |||||
| chr2:85193969
|
A | T | 49 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(46): Show | 49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+59519A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193969 | ||||||
| chr2:85194246
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.441+59796A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194246 | ||||||
| chr2:85194260
|
G | C | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+59810G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194260 | ||||||
| chr2:85194300
|
G | A | 13 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+59850G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194300 | ||||||
| chr2:85194398
|
G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+59948G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194398 | ||||||
| chr2:85194568
|
A | G | 49 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(46): Show | 49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+60118A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194568 | ||||||
| chr2:85194618
|
C | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0209 | 2 | HG00597.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.441+60168C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194618 | ||||||
| chr2:85194657
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.441+60207G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194657 | ||||||
| chr2:85194670
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0005g0001a0001c0001t0006g0003 | 3 | HG00741.hp2 HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.441+60220A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194670 | ||||||
| chr2:85194783
|
G | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+60333G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194783 | ||||||
| chr2:85194784
|
A | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+60334A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194784 | ||||||
| chr2:85194850
|
C | T | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441+60400C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194850 | ||||||
| chr2:85195062
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.441+60612G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195062 | ||||||
| chr2:85195191
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.441+60741A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195191 | ||||||
| chr2:85195299
|
C | T | 35 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(32): Show | 35 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.441+60849C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195299 | ||||||
| chr2:85195413
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+60963G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195413 | ||||||
| chr2:85195494
|
C | T | 8 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(5): Show | 8 | HG02572.hp2 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+61044C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195494 | ||||||
| chr2:85195649
|
A | G | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+61199A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195649 | ||||||
| chr2:85195695
|
C | T | 85 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(82): Show | 85 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.441+61245C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195695 | ||||||
| chr2:85195860
|
T | C | 49 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(46): Show | 49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+61410T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195860 | ||||||
| chr2:85195870
|
A | C | 35 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(32): Show | 35 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.441+61420A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195870 | ||||||
| chr2:85195915
|
T | A | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+61465T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195915 | ||||||
| chr2:85196072
|
T | C | 13 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+61622T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196072 | ||||||
| chr2:85196195
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.441+61745G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196195 | ||||||
| chr2:85196291
|
C | T | 13 | a0001c0001t0001g0122a0001c0001t0001g0145a0001c0001t0001g0160others(10): Show | 13 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+61841C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196291 | ||||||
| chr2:85196454
|
C | G | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+62004C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196454 | ||||||
| chr2:85196474
|
G | A | 3 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0060 | 3 | HG00738.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.441+62024G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196474 | ||||||
| chr2:85196537
|
A | AT | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02258.hp1 HG03041.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+62101dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85196537 | |||||
| chr2:85196537
|
AT | A | 13 | a0001c0001t0001g0076a0001c0001t0001g0171a0001c0001t0001g0234others(10): Show | 13 | HG00735.hp1 HG01175.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+62101delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85196537 | |||||
| chr2:85196657
|
A | C | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.441+62207A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196657 | ||||||
| chr2:85196751
|
A | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+62301A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196751 | ||||||
| chr2:85196895
|
C | T | 29 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.441+62445C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196895 | ||||||
| chr2:85196944
|
C | T | 33 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(30): Show | 33 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.441+62494C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196944 | ||||||
| chr2:85197001
|
G | T | 1 | a0002c0002t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+62551G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197001 | ||||||
| chr2:85197007
|
C | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(10): Show | 13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+62557C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197007 | ||||||
| chr2:85197176
|
C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+62726C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197176 | ||||||
| chr2:85197177
|
G | A | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.441+62727G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197177 | ||||||
| chr2:85197437
|
A | C | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441+62987A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197437 | ||||||
| chr2:85197670
|
T | C | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+63220T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197670 | ||||||
| chr2:85197702
|
A | G | 28 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+63252A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197702 | ||||||
| chr2:85197731
|
C | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+63281C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197731 | ||||||
| chr2:85197784
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0002g0141a0002c0002t0001g0093others(1): Show | 4 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+63334C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197784 | ||||||
| chr2:85197864
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.441+63414A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197864 | ||||||
| chr2:85197925
|
T | C | 59 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(56): Show | 59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.441+63475T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197925 | ||||||
| chr2:85198215
|
C | G | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+63765C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198215 | ||||||
| chr2:85198237
|
T | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+63787T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198237 | ||||||
| chr2:85198690
|
G | A | 3 | a0001c0001t0002g0167a0001c0001t0002g0174a0001c0001t0002g0175 | 3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+64240G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198690 | ||||||
| chr2:85198730
|
A | T | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0002c0002t0002g0058others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+64280A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198730 | ||||||
| chr2:85198985
|
G | GT | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02572.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+64541dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85198985 | |||||
| chr2:85199084
|
CT | C | 2 | a0001c0001t0001g0188a0001c0001t0002g0191 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.441+64635delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199084 | ||||||
| chr2:85199146
|
T | C | 28 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+64696T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199146 | ||||||
| chr2:85199286
|
G | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+64836G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199286 | ||||||
| chr2:85199340
|
A | G | 28 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+64890A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199340 | ||||||
| chr2:85199601
|
G | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+65151G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199601 | ||||||
| chr2:85199704
|
C | T | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441+65254C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199704 | ||||||
| chr2:85199986
|
G | A | 113 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(110): Show | 113 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.441+65536G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199986 | ||||||
| chr2:85200127
|
CA | C | 4 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082others(1): Show | 4 | HG02258.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+65678delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200127 | ||||||
| chr2:85200580
|
A | G | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+66130A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200580 | ||||||
| chr2:85200677
|
G | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+66227G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200677 | ||||||
| chr2:85200818
|
ATACCTGC others(11): Show |
A | 3 | a0001c0001t0001g0144a0001c0001t0001g0223a0008c0013t0001g0143 | 3 | HG02129.hp1 HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.441+66406_441+6642 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85200818 | |||||
| chr2:85200869
|
G | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+66419G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200869 | ||||||
| chr2:85201129
|
G | C | 3 | a0001c0001t0001g0144a0001c0001t0001g0223a0008c0013t0001g0143 | 3 | HG02129.hp1 HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.441+66679G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201129 | ||||||
| chr2:85201197
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+66747C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201197 | ||||||
| chr2:85201271
|
A | G | 37 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(34): Show | 37 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.441+66821A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201271 | ||||||
| chr2:85201272
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.441+66822G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201272 | ||||||
| chr2:85201462
|
T | G | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.441+67012T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201462 | ||||||
| chr2:85201604
|
G | T | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+67154G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201604 | ||||||
| chr2:85201720
|
G | A | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.441+67270G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201720 | ||||||
| chr2:85201737
|
C | T | 48 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(45): Show | 48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.441+67287C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201737 | ||||||
| chr2:85201937
|
TTTTA | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0210a0002c0002t0002g0017others(2): Show | 5 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+67515_441+6751 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85201937 | |||||
| chr2:85201937
|
TTTTATTT others(1): Show |
T | 133 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(130): Show | 133 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.441+67511_441+6751 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85201937 | |||||
| chr2:85201950
|
T | G | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+67500T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201950 | ||||||
| chr2:85202025
|
C | T | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+67575C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202025 | ||||||
| chr2:85202075
|
G | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+67625G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202075 | ||||||
| chr2:85202099
|
A | G | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+67649A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202099 | ||||||
| chr2:85202316
|
G | A | 1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441+67866G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202316 | ||||||
| chr2:85202377
|
T | C | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+67927T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202377 | ||||||
| chr2:85202454
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+68004A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202454 | ||||||
| chr2:85202502
|
T | C | 32 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+68052T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202502 | ||||||
| chr2:85202690
|
T | A | 1 | a0002c0002t0003g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.441+68240T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202690 | ||||||
| chr2:85202865
|
G | A | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+68415G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202865 | ||||||
| chr2:85202902
|
A | C | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.441+68452A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202902 | ||||||
| chr2:85202960
|
A | T | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+68510A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202960 | ||||||
| chr2:85202979
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.441+68529A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202979 | ||||||
| chr2:85203037
|
A | G | 1 | a0002c0002t0001g0023 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.441+68587A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203037 | ||||||
| chr2:85203056
|
T | C | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+68606T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203056 | ||||||
| chr2:85203081
|
C | T | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+68631C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203081 | ||||||
| chr2:85203270
|
A | G | 1 | a0011c0017t0001g0220 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.441+68820A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203270 | ||||||
| chr2:85203446
|
A | G | 6 | a0001c0001t0001g0121a0001c0001t0001g0210a0002c0002t0002g0017others(3): Show | 6 | HG02572.hp1 HG03225.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+68996A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203446 | ||||||
| chr2:85203447
|
T | C | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+68997T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203447 | ||||||
| chr2:85203465
|
G | A | 34 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(31): Show | 34 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+69015G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203465 | ||||||
| chr2:85203511
|
A | G | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69061A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203511 | ||||||
| chr2:85203572
|
A | T | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69122A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203572 | ||||||
| chr2:85203576
|
T | A | 24 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(21): Show | 24 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+69126T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203576 | ||||||
| chr2:85203746
|
A | G | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69296A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203746 | ||||||
| chr2:85203862
|
C | T | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69412C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203862 | ||||||
| chr2:85203889
|
C | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(10): Show | 13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+69439C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203889 | ||||||
| chr2:85203926
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.441+69476C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203926 | ||||||
| chr2:85204291
|
T | TC | 44 | a0001c0001t0001g0088a0001c0001t0001g0110a0001c0001t0001g0113others(41): Show | 44 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.441+69855dupC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | |||||
| chr2:85204291
|
T | TCC | 69 | a0001c0001t0001g0076a0001c0001t0001g0092a0001c0001t0001g0095others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.441+69854_441+6985 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | |||||
| chr2:85204291
|
T | TCCC | 24 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0122others(21): Show | 24 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+69853_441+6985 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | |||||
| chr2:85204291
|
TC | T | 18 | a0001c0001t0001g0109a0001c0001t0001g0218a0001c0001t0001g0229others(15): Show | 18 | HG00735.hp1 HG00741.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+69855delC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | |||||
| chr2:85204296
|
C | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+69846C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204296 | ||||||
| chr2:85204334
|
G | C | 2 | a0001c0001t0002g0134a0002c0002t0001g0118 | 2 | NA18959.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.441+69884G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204334 | ||||||
| chr2:85204420
|
G | A | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69970G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204420 | ||||||
| chr2:85204618
|
CA | C | 32 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+70171delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204618 | |||||
| chr2:85204831
|
AT | A | 14 | a0001c0001t0001g0133a0001c0001t0001g0161a0001c0001t0001g0163others(11): Show | 14 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+70392delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204831 | |||||
| chr2:85204844
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+70394A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204844 | ||||||
| chr2:85204883
|
T | G | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+70433T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204883 | ||||||
| chr2:85204884
|
TG | T | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(7): Show | 10 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+70435delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204884 | ||||||
| chr2:85204885
|
G | GT | 105 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(102): Show | 105 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.441+70438dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204885 | |||||
| chr2:85204885
|
G | T | 1 | a0001c0001t0002g0167 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.441+70435G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204885 | ||||||
| chr2:85204889
|
G | T | 133 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(130): Show | 133 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.441+70439G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204889 | ||||||
| chr2:85204931
|
C | G | 1 | a0002c0002t0002g0028 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.441+70481C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204931 | ||||||
| chr2:85205281
|
A | C | 28 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+70831A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205281 | ||||||
| chr2:85205337
|
T | C | 28 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+70887T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205337 | ||||||
| chr2:85205466
|
G | C | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+71016G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205466 | ||||||
| chr2:85205535
|
T | TTC | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+71086_441+7108 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85205535 | |||||
| chr2:85205536
|
TG | T | 108 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(105): Show | 108 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.441+71087delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205536 | ||||||
| chr2:85205537
|
G | C | 16 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0210others(13): Show | 16 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+71087G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205537 | ||||||
| chr2:85205537
|
G | T | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+71087G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205537 | ||||||
| chr2:85205538
|
T | C | 108 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(105): Show | 108 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.441+71088T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205538 | ||||||
| chr2:85205539
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.441+71089T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205539 | ||||||
| chr2:85205580
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.441+71130G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205580 | ||||||
| chr2:85205702
|
G | A | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+71252G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205702 | ||||||
| chr2:85205737
|
T | C | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+71287T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205737 | ||||||
| chr2:85205818
|
G | C | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+71368G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205818 | ||||||
| chr2:85205827
|
T | C | 31 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(28): Show | 31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+71377T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205827 | ||||||
| chr2:85205969
|
A | G | 2 | a0001c0001t0001g0107a0002c0002t0001g0034 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.441+71519A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205969 | ||||||
| chr2:85206064
|
T | C | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+71614T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206064 | ||||||
| chr2:85206147
|
G | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(29): Show | 32 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+71697G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206147 | ||||||
| chr2:85206279
|
G | A | 28 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+71829G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206279 | ||||||
| chr2:85206300
|
C | T | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+71850C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206300 | ||||||
| chr2:85206343
|
T | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+71893T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206343 | ||||||
| chr2:85206471
|
T | C | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.441+72021T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206471 | ||||||
| chr2:85206670
|
G | T | 24 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(21): Show | 24 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+72220G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206670 | ||||||
| chr2:85206724
|
T | C | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+72274T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206724 | ||||||
| chr2:85206833
|
A | G | 10 | a0001c0001t0001g0149a0001c0001t0001g0188a0001c0001t0001g0190others(7): Show | 10 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+72383A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206833 | ||||||
| chr2:85206966
|
AAC | A | 48 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(45): Show | 48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.441+72518_441+7251 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85206966 | |||||
| chr2:85206981
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+72531C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206981 | ||||||
| chr2:85206985
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.441+72535C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206985 | ||||||
| chr2:85207250
|
A | G | 1 | a0002c0002t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.441+72800A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207250 | ||||||
| chr2:85207309
|
A | C | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+72859A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207309 | ||||||
| chr2:85207372
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+72922C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207372 | ||||||
| chr2:85207417
|
C | T | 212 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0076others(209): Show | 212 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(209): Show |
intron_variant | MODIFIER | c.441+72967C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207417 | ||||||
| chr2:85207446
|
T | C | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+72996T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207446 | ||||||
| chr2:85207489
|
A | G | 48 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(45): Show | 48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.441+73039A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207489 | ||||||
| chr2:85207654
|
G | A | 25 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(22): Show | 25 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.441+73204G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207654 | ||||||
| chr2:85207699
|
T | G | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+73249T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207699 | ||||||
| chr2:85207706
|
A | G | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441+73256A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207706 | ||||||
| chr2:85207807
|
C | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+73357C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207807 | ||||||
| chr2:85207916
|
T | G | 30 | a0001c0001t0001g0031a0001c0001t0001g0110a0001c0001t0001g0111others(27): Show | 30 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+73466T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207916 | ||||||
| chr2:85207997
|
C | T | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(10): Show | 13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+73547C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207997 | ||||||
| chr2:85207999
|
C | T | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+73549C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207999 | ||||||
| chr2:85208031
|
T | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+73581T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208031 | ||||||
| chr2:85208101
|
T | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+73651T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208101 | ||||||
| chr2:85208158
|
G | A | 12 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(9): Show | 12 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+73708G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208158 | ||||||
| chr2:85208239
|
G | A | 14 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(11): Show | 14 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+73789G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208239 | ||||||
| chr2:85208346
|
A | G | 14 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(11): Show | 14 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+73896A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208346 | ||||||
| chr2:85208574
|
A | G | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+74124A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208574 | ||||||
| chr2:85208611
|
T | C | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+74161T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208611 | ||||||
| chr2:85208821
|
A | G | 140 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(137): Show | 140 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.441+74371A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208821 | ||||||
| chr2:85208827
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+74377A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208827 | ||||||
| chr2:85208998
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.442-74497G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208998 | ||||||
| chr2:85209052
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.442-74443G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209052 | ||||||
| chr2:85209162
|
GT | G | 127 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(124): Show | 127 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.442-74331delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85209162 | |||||
| chr2:85209423
|
G | A | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-74072G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209423 | ||||||
| chr2:85209583
|
G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-73912G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209583 | ||||||
| chr2:85209691
|
C | A | 2 | a0003c0003t0002g0086a0005c0012t0002g0184 | 2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.442-73804C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209691 | ||||||
| chr2:85209761
|
C | T | 31 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(28): Show | 31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.442-73734C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209761 | ||||||
| chr2:85210297
|
G | T | 116 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(113): Show | 116 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.442-73198G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210297 | ||||||
| chr2:85210314
|
A | G | 116 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(113): Show | 116 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.442-73181A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210314 | ||||||
| chr2:85210361
|
G | A | 28 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(25): Show | 28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-73134G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210361 | ||||||
| chr2:85210443
|
C | T | 1 | a0002c0002t0002g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.442-73052C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210443 | ||||||
| chr2:85210614
|
G | A | 3 | a0001c0001t0002g0202a0002c0002t0001g0037a0002c0002t0003g0084 | 3 | HG02809.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.442-72881G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210614 | ||||||
| chr2:85210694
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-72801G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210694 | ||||||
| chr2:85210822
|
C | T | 110 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(107): Show | 110 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.442-72673C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210822 | ||||||
| chr2:85210877
|
G | A | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-72618G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210877 | ||||||
| chr2:85210942
|
C | T | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-72553C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210942 | ||||||
| chr2:85210944
|
C | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-72551C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210944 | ||||||
| chr2:85211153
|
A | G | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-72342A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85211153 | ||||||
| chr2:85211224
|
TA | T | 87 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(84): Show | 87 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.442-72269delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85211224 | |||||
| chr2:85211417
|
C | T | 31 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0101others(28): Show | 31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.442-72078C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85211417 | ||||||
| chr2:85211786
|
G | T | 123 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(120): Show | 123 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.442-71709G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85211786 | ||||||
| chr2:85212046
|
C | T | 34 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(31): Show | 34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-71449C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212046 | ||||||
| chr2:85212089
|
C | CA | 19 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0200others(16): Show | 19 | HG00621.hp1 HG00735.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-71379dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | |||||
| chr2:85212089
|
C | CAA | 18 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0102others(15): Show | 18 | HG00597.hp1 HG01071.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-71380_442-7137 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | |||||
| chr2:85212089
|
CA | C | 75 | a0001c0001t0001g0014a0001c0001t0001g0097a0001c0001t0001g0113others(72): Show | 75 | HG00280.hp1 HG00621.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.442-71379delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | |||||
| chr2:85212089
|
CAA | C | 57 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0096others(54): Show | 57 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.442-71380_442-7137 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | |||||
| chr2:85212089
|
CAAA | C | 8 | a0001c0001t0002g0165a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 8 | HG01167.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-71381_442-7137 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | |||||
| chr2:85212089
|
CAAAAAAA others(1): Show |
C | 27 | a0001c0001t0001g0090a0001c0001t0001g0122a0001c0001t0001g0145others(24): Show | 27 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-71386_442-7137 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | |||||
| chr2:85212089
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-71392_442-7137 others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | |||||
| chr2:85212220
|
C | T | 4 | a0001c0001t0001g0219a0001c0001t0002g0103a0002c0002t0001g0022others(1): Show | 4 | HG01071.hp1 HG01346.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-71275C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212220 | ||||||
| chr2:85212430
|
T | C | 136 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(133): Show | 136 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.442-71065T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212430 | ||||||
| chr2:85212650
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.442-70845G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212650 | ||||||
| chr2:85212748
|
A | G | 38 | a0001c0001t0001g0031a0001c0001t0001g0091a0001c0001t0001g0095others(35): Show | 38 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.442-70747A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212748 | ||||||
| chr2:85212828
|
C | A | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-70667C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212828 | ||||||
| chr2:85212867
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-70628A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212867 | ||||||
| chr2:85213026
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442-70469G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213026 | ||||||
| chr2:85213043
|
G | A | 3 | a0001c0001t0001g0210a0003c0003t0002g0086a0005c0012t0002g0184 | 3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.442-70452G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213043 | ||||||
| chr2:85213275
|
A | G | 141 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(138): Show | 141 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(138): Show |
intron_variant | MODIFIER | c.442-70220A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213275 | ||||||
| chr2:85213300
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-70195A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213300 | ||||||
| chr2:85213713
|
T | C | 15 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(12): Show | 15 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-69782T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213713 | ||||||
| chr2:85214106
|
G | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-69389G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214106 | ||||||
| chr2:85214112
|
C | A | 2 | a0002c0002t0001g0042a0002c0002t0002g0044 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.442-69383C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214112 | ||||||
| chr2:85214137
|
G | T | 1 | a0002c0002t0002g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.442-69358G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214137 | ||||||
| chr2:85214248
|
T | C | 1 | a0002c0002t0001g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.442-69247T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214248 | ||||||
| chr2:85214276
|
A | G | 46 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0109others(43): Show | 46 | HG00280.hp1 HG00621.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-69219A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214276 | ||||||
| chr2:85214689
|
A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-68806A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214689 | ||||||
| chr2:85214728
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-68767G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214728 | ||||||
| chr2:85214748
|
A | G | 12 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(9): Show | 12 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-68747A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214748 | ||||||
| chr2:85214815
|
T | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-68680T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214815 | ||||||
| chr2:85214945
|
T | A | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-68550T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214945 | ||||||
| chr2:85214958
|
A | G | 1 | a0001c0001t0002g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.442-68537A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214958 | ||||||
| chr2:85215057
|
C | T | 11 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(8): Show | 11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-68438C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215057 | ||||||
| chr2:85215161
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0002g0185a0001c0001t0002g0205others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-68334C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215161 | ||||||
| chr2:85215167
|
C | G | 28 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0140others(25): Show | 28 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-68328C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215167 | ||||||
| chr2:85215213
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.442-68282T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215213 | ||||||
| chr2:85215227
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.442-68268G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215227 | ||||||
| chr2:85215365
|
A | G | 28 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0140others(25): Show | 28 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-68130A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215365 | ||||||
| chr2:85215617
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0167others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-67878G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215617 | ||||||
| chr2:85215767
|
T | TG | 20 | a0001c0001t0001g0031a0001c0001t0001g0121a0001c0001t0001g0131others(17): Show | 20 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.442-67719dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85215767 | |||||
| chr2:85215767
|
TG | T | 16 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(13): Show | 16 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-67719delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85215767 | |||||
| chr2:85215916
|
C | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-67579C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215916 | ||||||
| chr2:85216047
|
G | C | 21 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(18): Show | 21 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-67448G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216047 | ||||||
| chr2:85216246
|
G | A | 40 | a0001c0001t0001g0031a0001c0001t0001g0096a0001c0001t0001g0133others(37): Show | 40 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.442-67249G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216246 | ||||||
| chr2:85216256
|
G | A | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-67239G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216256 | ||||||
| chr2:85216420
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01256.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-67075G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216420 | ||||||
| chr2:85216527
|
G | A | 154 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(151): Show | 154 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.442-66968G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216527 | ||||||
| chr2:85216583
|
T | C | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-66912T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216583 | ||||||
| chr2:85216625
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-66870G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216625 | ||||||
| chr2:85216669
|
G | T | 2 | a0003c0003t0002g0086a0005c0012t0002g0184 | 2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.442-66826G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216669 | ||||||
| chr2:85216697
|
G | A | 26 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0140others(23): Show | 26 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.442-66798G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216697 | ||||||
| chr2:85216711
|
G | T | 2 | a0003c0003t0002g0086a0005c0012t0002g0184 | 2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.442-66784G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216711 | ||||||
| chr2:85216801
|
G | A | 94 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0096others(91): Show | 94 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.442-66694G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216801 | ||||||
| chr2:85216962
|
C | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-66533C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216962 | ||||||
| chr2:85217252
|
C | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-66243C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217252 | ||||||
| chr2:85217456
|
C | T | 22 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0101others(19): Show | 22 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-66039C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217456 | ||||||
| chr2:85217604
|
C | G | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(6): Show | 9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-65891C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217604 | ||||||
| chr2:85217781
|
A | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-65714A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217781 | ||||||
| chr2:85218236
|
T | TTTTA | 47 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(44): Show | 47 | HG01106.hp2 HG01175.hp2 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.442-65227_442-6522 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | |||||
| chr2:85218236
|
T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0206a0002c0002t0001g0057a0002c0007t0002g0029others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-65231_442-6522 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | |||||
| chr2:85218236
|
T | TTTTATTT others(5): Show |
1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.442-65235_442-6522 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | |||||
| chr2:85218236
|
T | TTTTATTT others(9): Show |
8 | a0001c0001t0001g0234a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 8 | HG00735.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-65239_442-6522 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | |||||
| chr2:85218403
|
A | T | 13 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(10): Show | 13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-65092A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218403 | ||||||
| chr2:85218548
|
G | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64947G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218548 | ||||||
| chr2:85218638
|
A | AG | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64857_442-6485 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218638 | ||||||
| chr2:85218639
|
T | G | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64856T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218639 | ||||||
| chr2:85218639
|
T | TGG | 16 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0135others(13): Show | 16 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-64848_442-6484 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218639 | |||||
| chr2:85218648
|
G | A | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173others(1): Show | 4 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-64847G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218648 | ||||||
| chr2:85218649
|
A | G | 41 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0145others(38): Show | 41 | HG00280.hp2 HG00735.hp1 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.442-64846A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218649 | ||||||
| chr2:85218650
|
A | G | 6 | a0001c0001t0001g0031a0001c0001t0002g0194a0001c0001t0002g0195others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-64845A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218650 | ||||||
| chr2:85218762
|
T | C | 4 | a0001c0001t0001g0206a0001c0001t0002g0185a0001c0001t0002g0205others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-64733T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218762 | ||||||
| chr2:85218993
|
G | A | 2 | a0001c0001t0001g0179a0002c0002t0003g0078 | 2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.442-64502G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218993 | ||||||
| chr2:85219043
|
C | T | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-64452C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219043 | ||||||
| chr2:85219066
|
T | C | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64429T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219066 | ||||||
| chr2:85219161
|
A | AT | 13 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(10): Show | 13 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-64326dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85219161 | |||||
| chr2:85219169
|
T | C | 19 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0145others(16): Show | 19 | HG01934.hp2 HG02056.hp2 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-64326T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219169 | ||||||
| chr2:85219321
|
A | G | 32 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(29): Show | 32 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.442-64174A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219321 | ||||||
| chr2:85219363
|
A | G | 94 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0096others(91): Show | 94 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.442-64132A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219363 | ||||||
| chr2:85219398
|
A | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-64097A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219398 | ||||||
| chr2:85219402
|
CA | C | 2 | a0002c0002t0001g0069a0002c0002t0001g0081 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-64091delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85219402 | |||||
| chr2:85219560
|
C | G | 1 | a0002c0002t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.442-63935C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219560 | ||||||
| chr2:85219876
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442-63619G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219876 | ||||||
| chr2:85219901
|
T | A | 32 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(29): Show | 32 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.442-63594T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219901 | ||||||
| chr2:85219940
|
A | G | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-63555A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219940 | ||||||
| chr2:85220217
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-63278A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220217 | ||||||
| chr2:85220320
|
T | G | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(6): Show | 9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-63175T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220320 | ||||||
| chr2:85220359
|
A | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-63136A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220359 | ||||||
| chr2:85220361
|
A | T | 160 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(157): Show | 160 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.442-63134A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220361 | ||||||
| chr2:85220393
|
T | C | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(6): Show | 9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-63102T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220393 | ||||||
| chr2:85220412
|
A | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-63083A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220412 | ||||||
| chr2:85220449
|
A | ACCT | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(6): Show | 9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-63040_442-6303 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85220449 | |||||
| chr2:85220586
|
G | A | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-62909G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220586 | ||||||
| chr2:85220600
|
G | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-62895G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220600 | ||||||
| chr2:85220707
|
C | T | 133 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(130): Show | 133 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.442-62788C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220707 | ||||||
| chr2:85220807
|
G | C | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-62688G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220807 | ||||||
| chr2:85220896
|
A | G | 1 | a0006c0006t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.442-62599A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220896 | ||||||
| chr2:85221102
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-62393C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221102 | ||||||
| chr2:85221233
|
G | A | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(6): Show | 9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-62262G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221233 | ||||||
| chr2:85221368
|
A | G | 4 | a0001c0001t0001g0206a0001c0001t0002g0185a0001c0001t0002g0205others(1): Show | 4 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-62127A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221368 | ||||||
| chr2:85221372
|
G | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-62123G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221372 | ||||||
| chr2:85221380
|
T | C | 235 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(232): Show | 235 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(232): Show |
intron_variant | MODIFIER | c.442-62115T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221380 | ||||||
| chr2:85221507
|
G | C | 4 | a0001c0001t0001g0088a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-61988G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221507 | ||||||
| chr2:85221546
|
A | G | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-61949A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221546 | ||||||
| chr2:85221557
|
G | A | 2 | a0002c0002t0001g0037a0002c0002t0003g0084 | 2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.442-61938G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221557 | ||||||
| chr2:85221732
|
C | G | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(6): Show | 9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-61763C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221732 | ||||||
| chr2:85221899
|
A | G | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-61596A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221899 | ||||||
| chr2:85221913
|
A | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-61582A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221913 | ||||||
| chr2:85221931
|
T | TA | 85 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0096others(82): Show | 85 | HG00597.hp2 HG00735.hp1 HG01071.hp2 others(82): Show |
intron_variant | MODIFIER | c.442-61550dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85221931 | |||||
| chr2:85221956
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-61539A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221956 | ||||||
| chr2:85221992
|
G | A | 1 | a0002c0002t0002g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.442-61503G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221992 | ||||||
| chr2:85222069
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.442-61426C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222069 | ||||||
| chr2:85222108
|
G | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-61387G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222108 | ||||||
| chr2:85222197
|
C | T | 17 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0140others(14): Show | 17 | HG00597.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-61298C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222197 | ||||||
| chr2:85222201
|
C | T | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-61294C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222201 | ||||||
| chr2:85222256
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-61239G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222256 | ||||||
| chr2:85222311
|
G | C | 1 | a0002c0002t0012g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.442-61184G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222311 | ||||||
| chr2:85222348
|
A | AC | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-61147_442-6114 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222348 | ||||||
| chr2:85222348
|
A | C | 13 | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0001t0001g0163others(10): Show | 13 | HG00639.hp2 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-61147A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222348 | ||||||
| chr2:85222351
|
A | C | 1 | a0001c0001t0001g0216 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.442-61144A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222351 | ||||||
| chr2:85222352
|
C | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-61143C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222352 | ||||||
| chr2:85222361
|
AAAC | A | 18 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0099others(15): Show | 18 | HG00280.hp2 HG01106.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-61131_442-6112 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222361 | |||||
| chr2:85222364
|
C | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0216a0002c0002t0002g0017 | 3 | HG02056.hp1 HG06807.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.442-61131C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222364 | ||||||
| chr2:85222368
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.442-61127A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222368 | ||||||
| chr2:85222375
|
A | C | 32 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(29): Show | 32 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.442-61120A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222375 | ||||||
| chr2:85222417
|
C | A | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.442-61078C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222417 | ||||||
| chr2:85222485
|
T | C | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-61010T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222485 | ||||||
| chr2:85222534
|
G | A | 1 | a0002c0002t0001g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-60961G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222534 | ||||||
| chr2:85222600
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.442-60895G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222600 | ||||||
| chr2:85222618
|
C | G | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-60877C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222618 | ||||||
| chr2:85222669
|
C | CA | 26 | a0001c0001t0001g0076a0001c0001t0001g0109a0001c0001t0001g0122others(23): Show | 26 | HG00735.hp2 HG02129.hp1 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.442-60806dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | |||||
| chr2:85222669
|
C | CAA | 54 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0096others(51): Show | 54 | HG00597.hp2 HG01243.hp1 HG01934.hp2 others(51): Show |
intron_variant | MODIFIER | c.442-60807_442-6080 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | |||||
| chr2:85222669
|
C | CAAA | 14 | a0001c0001t0001g0149a0001c0001t0001g0156a0001c0001t0001g0188others(11): Show | 14 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-60808_442-6080 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | |||||
| chr2:85222669
|
C | CAAAA | 14 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0193others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-60809_442-6080 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | |||||
| chr2:85222669
|
C | CAAAAA | 7 | a0001c0001t0001g0234a0002c0002t0001g0040a0002c0002t0001g0061others(4): Show | 7 | HG00735.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-60810_442-6080 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | |||||
| chr2:85222685
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.442-60810A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222685 | ||||||
| chr2:85222909
|
G | A | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-60586G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222909 | ||||||
| chr2:85223212
|
G | A | 1 | a0002c0002t0001g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.442-60283G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223212 | ||||||
| chr2:85223238
|
C | T | 16 | a0001c0001t0001g0096a0001c0001t0001g0133a0001c0001t0001g0140others(13): Show | 16 | HG00597.hp2 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-60257C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223238 | ||||||
| chr2:85223486
|
G | A | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-60009G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223486 | ||||||
| chr2:85223582
|
T | TG | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.442-59911dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85223582 | |||||
| chr2:85223691
|
G | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0188a0001c0001t0001g0190others(10): Show | 13 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-59804G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223691 | ||||||
| chr2:85223813
|
A | G | 4 | a0001c0001t0001g0210a0002c0002t0002g0017a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-59682A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223813 | ||||||
| chr2:85223836
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0002g0191 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.442-59659C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223836 | ||||||
| chr2:85224018
|
A | T | 6 | a0001c0001t0001g0232a0001c0001t0002g0067a0002c0002t0001g0009others(3): Show | 6 | HG02451.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-59477A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224018 | ||||||
| chr2:85224123
|
G | C | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-59372G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224123 | ||||||
| chr2:85224238
|
A | G | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-59257A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224238 | ||||||
| chr2:85224424
|
A | C | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-59071A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224424 | ||||||
| chr2:85224540
|
A | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-58955A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224540 | ||||||
| chr2:85224760
|
T | C | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-58735T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224760 | ||||||
| chr2:85224997
|
T | C | 3 | a0001c0001t0002g0125a0002c0002t0001g0056a0002c0002t0002g0047 | 3 | NA18951.hp2 NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.442-58498T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224997 | ||||||
| chr2:85225623
|
A | AT | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0002c0002t0002g0058others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-57868dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85225623 | |||||
| chr2:85225854
|
C | T | 1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.442-57641C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85225854 | ||||||
| chr2:85225855
|
G | A | 2 | a0002c0002t0001g0089a0002c0002t0002g0043 | 2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.442-57640G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85225855 | ||||||
| chr2:85225988
|
T | C | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-57507T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85225988 | ||||||
| chr2:85226448
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-57047A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226448 | ||||||
| chr2:85226470
|
T | C | 90 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0096others(87): Show | 90 | HG00597.hp2 HG00735.hp1 HG01071.hp2 others(87): Show |
intron_variant | MODIFIER | c.442-57025T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226470 | ||||||
| chr2:85226544
|
G | GT | 12 | a0001c0001t0001g0031a0001c0001t0001g0188a0001c0001t0001g0190others(9): Show | 12 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-56947dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226544 | |||||
| chr2:85226590
|
T | TCTC | 157 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0076others(154): Show | 157 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(154): Show |
intron_variant | MODIFIER | c.442-56905_442-5690 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226590 | ||||||
| chr2:85226737
|
A | G | 34 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(31): Show | 34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-56758A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226737 | ||||||
| chr2:85226816
|
CT | C | 46 | a0001c0001t0001g0031a0001c0001t0001g0096a0001c0001t0001g0117others(43): Show | 46 | HG00597.hp2 HG01071.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-56661delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226816 | |||||
| chr2:85226816
|
CTT | C | 7 | a0001c0001t0001g0163a0001c0001t0001g0229a0001c0001t0002g0194others(4): Show | 7 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-56662_442-5666 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226816 | |||||
| chr2:85226816
|
CTTT | C | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0234others(5): Show | 8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-56663_442-5666 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226816 | |||||
| chr2:85226916
|
A | T | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56579A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226916 | ||||||
| chr2:85226972
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-56523C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226972 | ||||||
| chr2:85227134
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-56361G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227134 | ||||||
| chr2:85227165
|
A | G | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56330A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227165 | ||||||
| chr2:85227246
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0005g0001a0001c0001t0006g0003 | 3 | HG00741.hp2 HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.442-56249T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227246 | ||||||
| chr2:85227302
|
T | C | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56193T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227302 | ||||||
| chr2:85227438
|
C | CTT | 5 | a0001c0001t0001g0234a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56044_442-5604 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227438 | |||||
| chr2:85227438
|
CT | C | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01256.hp1 HG01517.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-56043delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227438 | |||||
| chr2:85227456
|
CAAGTAAG others(6): Show |
C | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.442-56035_442-5602 others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227456 | |||||
| chr2:85227551
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55944C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227551 | ||||||
| chr2:85227685
|
C | G | 14 | a0001c0001t0001g0031a0001c0001t0001g0149a0001c0001t0001g0188others(11): Show | 14 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-55810C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227685 | ||||||
| chr2:85227738
|
A | G | 18 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(15): Show | 18 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-55757A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227738 | ||||||
| chr2:85227764
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0002g0165 | 2 | HG01167.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.442-55731G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227764 | ||||||
| chr2:85227861
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55634G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227861 | ||||||
| chr2:85227925
|
A | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0182a0001c0001t0002g0165 | 3 | HG01167.hp1 HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.442-55570A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227925 | ||||||
| chr2:85227992
|
C | CA | 71 | a0001c0001t0001g0097a0001c0001t0001g0109a0001c0001t0001g0110others(68): Show | 71 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.442-55479dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227992 | |||||
| chr2:85227992
|
C | CAA | 13 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0132others(10): Show | 13 | HG00621.hp2 HG01175.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-55480_442-5547 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227992 | |||||
| chr2:85227992
|
CA | C | 24 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(21): Show | 24 | HG00735.hp1 HG01175.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.442-55479delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227992 | |||||
| chr2:85228017
|
T | A | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-55478T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228017 | ||||||
| chr2:85228035
|
A | G | 13 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(10): Show | 13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-55460A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228035 | ||||||
| chr2:85228048
|
A | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55447A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228048 | ||||||
| chr2:85228067
|
A | T | 1 | a0007c0011t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442-55428A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228067 | ||||||
| chr2:85228240
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.442-55255C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228240 | ||||||
| chr2:85228254
|
T | C | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55241T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228254 | ||||||
| chr2:85228336
|
C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-55159C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228336 | ||||||
| chr2:85228552
|
C | T | 34 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(31): Show | 34 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.442-54943C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228552 | ||||||
| chr2:85228763
|
C | T | 3 | a0001c0001t0001g0031a0002c0002t0001g0032a0002c0002t0001g0033 | 3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.442-54732C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228763 | ||||||
| chr2:85228816
|
C | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-54679C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228816 | ||||||
| chr2:85228831
|
C | T | 2 | a0002c0002t0001g0069a0002c0002t0001g0081 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-54664C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228831 | ||||||
| chr2:85228843
|
A | G | 87 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(84): Show | 87 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.442-54652A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228843 | ||||||
| chr2:85228978
|
G | A | 1 | a0002c0002t0002g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.442-54517G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228978 | ||||||
| chr2:85229015
|
T | C | 219 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0076others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(216): Show |
intron_variant | MODIFIER | c.442-54480T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229015 | ||||||
| chr2:85229020
|
C | CA | 37 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(34): Show | 37 | HG00597.hp2 HG00735.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-54456dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85229020 | |||||
| chr2:85229020
|
C | CAA | 21 | a0001c0001t0001g0031a0001c0001t0001g0188a0001c0001t0001g0190others(18): Show | 21 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.442-54457_442-5445 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85229020 | |||||
| chr2:85229020
|
CA | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0101a0002c0002t0001g0025others(2): Show | 5 | HG01975.hp1 HG02647.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-54456delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85229020 | |||||
| chr2:85229036
|
A | G | 1 | a0001c0001t0011g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.442-54459A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229036 | ||||||
| chr2:85229078
|
G | A | 2 | a0002c0002t0001g0061a0002c0002t0002g0062 | 2 | HG00735.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-54417G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229078 | ||||||
| chr2:85229085
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0002g0202a0002c0002t0001g0007others(9): Show | 12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-54410G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229085 | ||||||
| chr2:85229117
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.442-54378C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229117 | ||||||
| chr2:85229118
|
G | A | 9 | a0001c0001t0001g0232a0001c0001t0002g0067a0001c0001t0002g0167others(6): Show | 9 | HG02451.hp2 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-54377G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229118 | ||||||
| chr2:85229198
|
T | C | 34 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(31): Show | 34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-54297T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229198 | ||||||
| chr2:85229299
|
A | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-54196A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229299 | ||||||
| chr2:85229426
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.442-54069C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229426 | ||||||
| chr2:85229654
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0133 | 2 | NA18953.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.442-53841G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229654 | ||||||
| chr2:85229762
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-53733C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229762 | ||||||
| chr2:85229825
|
T | C | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-53670T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229825 | ||||||
| chr2:85230332
|
G | T | 2 | a0001c0001t0005g0001a0001c0001t0006g0003 | 2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.442-53163G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230332 | ||||||
| chr2:85230615
|
A | G | 22 | a0001c0001t0001g0156a0001c0001t0001g0170a0001c0001t0001g0171others(19): Show | 22 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.442-52880A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230615 | ||||||
| chr2:85230829
|
A | G | 34 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(31): Show | 34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-52666A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230829 | ||||||
| chr2:85230931
|
A | G | 28 | a0001c0001t0001g0156a0001c0001t0001g0170a0001c0001t0001g0171others(25): Show | 28 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-52564A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230931 | ||||||
| chr2:85231088
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.442-52407C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231088 | ||||||
| chr2:85231100
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-52395C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231100 | ||||||
| chr2:85231140
|
T | C | 3 | a0001c0001t0002g0138a0002c0002t0001g0064a0002c0002t0002g0063 | 3 | HG01074.hp2 HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.442-52355T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231140 | ||||||
| chr2:85231247
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.442-52248C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231247 | ||||||
| chr2:85231255
|
C | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(10): Show | 13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-52240C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231255 | ||||||
| chr2:85231534
|
T | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-51961T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231534 | ||||||
| chr2:85231654
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.442-51841C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231654 | ||||||
| chr2:85231655
|
G | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-51840G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231655 | ||||||
| chr2:85231777
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.442-51718C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231777 | ||||||
| chr2:85231778
|
G | A | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-51717G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231778 | ||||||
| chr2:85231913
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-51582C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231913 | ||||||
| chr2:85231972
|
GGATTGAG others(11): Show |
G | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-51520_442-5150 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85231972 | |||||
| chr2:85232071
|
A | G | 22 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(19): Show | 22 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-51424A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232071 | ||||||
| chr2:85232283
|
G | A | 1 | a0001c0001t0005g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.442-51212G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232283 | ||||||
| chr2:85232504
|
G | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-50991G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232504 | ||||||
| chr2:85232559
|
G | T | 34 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(31): Show | 34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-50936G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232559 | ||||||
| chr2:85232757
|
A | G | 80 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(77): Show | 80 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(77): Show |
intron_variant | MODIFIER | c.442-50738A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232757 | ||||||
| chr2:85232992
|
C | T | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-50503C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232992 | ||||||
| chr2:85233316
|
AT | A | 142 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(139): Show | 142 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.442-50160delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85233316 | |||||
| chr2:85233316
|
ATT | A | 30 | a0001c0001t0001g0031a0001c0001t0001g0156a0001c0001t0001g0161others(27): Show | 30 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.442-50161_442-5016 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85233316 | |||||
| chr2:85233316
|
ATTT | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(38): Show | 41 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.442-50162_442-5016 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85233316 | |||||
| chr2:85233382
|
T | C | 216 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0076others(213): Show | 216 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(213): Show |
intron_variant | MODIFIER | c.442-50113T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233382 | ||||||
| chr2:85233387
|
T | C | 83 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(80): Show | 83 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(80): Show |
intron_variant | MODIFIER | c.442-50108T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233387 | ||||||
| chr2:85233472
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.442-50023C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233472 | ||||||
| chr2:85233556
|
T | C | 84 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(81): Show | 84 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(81): Show |
intron_variant | MODIFIER | c.442-49939T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233556 | ||||||
| chr2:85233561
|
G | A | 2 | a0001c0001t0001g0226a0002c0002t0002g0020 | 2 | HG01346.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.442-49934G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233561 | ||||||
| chr2:85233813
|
G | A | 39 | a0001c0001t0001g0031a0001c0001t0001g0156a0001c0001t0001g0161others(36): Show | 39 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.442-49682G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233813 | ||||||
| chr2:85233827
|
C | T | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.442-49668C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233827 | ||||||
| chr2:85233917
|
C | T | 80 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(77): Show | 80 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(77): Show |
intron_variant | MODIFIER | c.442-49578C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233917 | ||||||
| chr2:85233943
|
G | A | 1 | a0002c0002t0002g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.442-49552G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233943 | ||||||
| chr2:85234020
|
TA | T | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-49472delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234020 | |||||
| chr2:85234094
|
C | G | 35 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(32): Show | 35 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.442-49401C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234094 | ||||||
| chr2:85234131
|
C | CT | 14 | a0001c0001t0001g0014a0001c0001t0001g0096a0001c0001t0001g0109others(11): Show | 14 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-49342dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234131 | |||||
| chr2:85234131
|
CT | C | 68 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0121others(65): Show | 68 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.442-49342delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234131 | |||||
| chr2:85234131
|
CTT | C | 15 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0002g0189others(12): Show | 15 | HG01167.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-49343_442-4934 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234131 | |||||
| chr2:85234153
|
T | C | 18 | a0001c0001t0001g0132a0001c0001t0001g0151a0001c0001t0001g0153others(15): Show | 18 | HG00741.hp1 HG01109.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-49342T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234153 | ||||||
| chr2:85234236
|
G | A | 41 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(38): Show | 41 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.442-49259G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234236 | ||||||
| chr2:85234709
|
A | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48786A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234709 | ||||||
| chr2:85234733
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48762C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234733 | ||||||
| chr2:85234886
|
T | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48609T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234886 | ||||||
| chr2:85234888
|
G | T | 1 | a0001c0001t0002g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.442-48607G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234888 | ||||||
| chr2:85235124
|
A | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48371A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235124 | ||||||
| chr2:85235125
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48370G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235125 | ||||||
| chr2:85235479
|
C | T | 54 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0109others(51): Show | 54 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.442-48016C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235479 | ||||||
| chr2:85235639
|
G | A | 7 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(4): Show | 7 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-47856G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235639 | ||||||
| chr2:85235650
|
G | A | 54 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0109others(51): Show | 54 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.442-47845G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235650 | ||||||
| chr2:85235888
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-47607T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235888 | ||||||
| chr2:85235995
|
C | CA | 7 | a0001c0001t0001g0210a0001c0001t0001g0234a0002c0002t0002g0017others(4): Show | 7 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-47492dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85235995 | |||||
| chr2:85236015
|
G | A | 10 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(7): Show | 10 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-47480G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236015 | ||||||
| chr2:85236046
|
G | A | 10 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(7): Show | 10 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-47449G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236046 | ||||||
| chr2:85236172
|
C | CT | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-47323_442-4732 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236172 | ||||||
| chr2:85236173
|
C | CA | 81 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(78): Show | 81 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(78): Show |
intron_variant | MODIFIER | c.442-47314dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85236173 | |||||
| chr2:85236176
|
A | AT | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-47319_442-4731 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236176 | ||||||
| chr2:85236176
|
A | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-47319A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236176 | ||||||
| chr2:85236259
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-47236T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236259 | ||||||
| chr2:85236386
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01256.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-47109G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236386 | ||||||
| chr2:85236662
|
C | T | 1 | a0002c0002t0003g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.442-46833C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236662 | ||||||
| chr2:85236705
|
A | G | 1 | a0004c0004t0002g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.442-46790A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236705 | ||||||
| chr2:85236850
|
C | G | 1 | a0001c0001t0011g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.442-46645C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236850 | ||||||
| chr2:85237032
|
C | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0224a0002c0002t0002g0065 | 3 | HG01934.hp2 HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.442-46463C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237032 | ||||||
| chr2:85237131
|
G | A | 6 | a0001c0001t0001g0210a0001c0001t0001g0234a0002c0002t0002g0017others(3): Show | 6 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-46364G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237131 | ||||||
| chr2:85237179
|
T | A | 1 | a0002c0002t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.442-46316T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237179 | ||||||
| chr2:85237188
|
A | G | 1 | a0010c0015t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442-46307A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237188 | ||||||
| chr2:85237370
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-46125G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237370 | ||||||
| chr2:85237403
|
C | T | 1 | a0010c0015t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442-46092C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237403 | ||||||
| chr2:85237416
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.442-46079C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237416 | ||||||
| chr2:85237469
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.442-46026A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237469 | ||||||
| chr2:85237553
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01256.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-45942A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237553 | ||||||
| chr2:85237559
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-45936C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237559 | ||||||
| chr2:85237795
|
C | A | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-45700C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237795 | ||||||
| chr2:85237880
|
T | C | 2 | a0002c0007t0002g0029a0003c0003t0002g0197 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-45615T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237880 | ||||||
| chr2:85237903
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.442-45592C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237903 | ||||||
| chr2:85238012
|
C | T | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-45483C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238012 | ||||||
| chr2:85238108
|
G | GCC | 22 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(19): Show | 22 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-45385_442-4538 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238108 | |||||
| chr2:85238127
|
G | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-45368G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238127 | ||||||
| chr2:85238400
|
A | C | 235 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(232): Show | 235 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(232): Show |
intron_variant | MODIFIER | c.442-45095A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238400 | ||||||
| chr2:85238408
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-45087G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238408 | ||||||
| chr2:85238648
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.442-44847A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238648 | ||||||
| chr2:85238652
|
G | A | 1 | a0003c0003t0002g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.442-44843G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238652 | ||||||
| chr2:85238708
|
G | A | 2 | a0001c0001t0001g0076a0002c0002t0003g0075 | 2 | NA18950.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.442-44787G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238708 | ||||||
| chr2:85238777
|
TTTTA | T | 82 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0092others(79): Show | 82 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.442-44666_442-4466 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | |||||
| chr2:85238777
|
TTTTATTT others(1): Show |
T | 96 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0091others(93): Show | 96 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.442-44670_442-4466 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | |||||
| chr2:85238777
|
TTTTATTT others(5): Show |
T | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0210others(7): Show | 10 | HG01071.hp1 HG01175.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-44674_442-4466 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | |||||
| chr2:85238777
|
TTTTATTT others(9): Show |
T | 3 | a0001c0001t0001g0153a0002c0002t0001g0069a0002c0002t0001g0081 | 3 | HG01975.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-44678_442-4466 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | |||||
| chr2:85238777
|
TTTTATTT others(13): Show |
T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-44682_442-4466 others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | |||||
| chr2:85238777
|
TTTTATTT others(17): Show |
T | 33 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(30): Show | 33 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.442-44686_442-4466 others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | |||||
| chr2:85239152
|
T | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-44343T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239152 | ||||||
| chr2:85239155
|
A | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-44340A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239155 | ||||||
| chr2:85239159
|
T | C | 3 | a0001c0001t0001g0015a0002c0002t0001g0168a0002c0002t0001g0172 | 3 | NA18950.hp2 NA19000.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.442-44336T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239159 | ||||||
| chr2:85239199
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.442-44296C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239199 | ||||||
| chr2:85239257
|
T | C | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-44238T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239257 | ||||||
| chr2:85239277
|
G | A | 2 | a0001c0001t0002g0106a0001c0016t0001g0186 | 2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-44218G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239277 | ||||||
| chr2:85239664
|
C | G | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-43831C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239664 | ||||||
| chr2:85239725
|
T | C | 1 | a0012c0010t0001g0207 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.442-43770T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239725 | ||||||
| chr2:85239741
|
G | A | 35 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(32): Show | 35 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.442-43754G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239741 | ||||||
| chr2:85239762
|
A | G | 122 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(119): Show | 122 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.442-43733A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239762 | ||||||
| chr2:85239802
|
G | A | 35 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(32): Show | 35 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.442-43693G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239802 | ||||||
| chr2:85239807
|
T | C | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-43688T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239807 | ||||||
| chr2:85239828
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.442-43667C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239828 | ||||||
| chr2:85239901
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0002c0002t0002g0058others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-43594G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239901 | ||||||
| chr2:85239933
|
G | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-43562G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239933 | ||||||
| chr2:85239944
|
T | TA | 6 | a0001c0001t0002g0195a0002c0002t0001g0040a0002c0002t0001g0089others(3): Show | 6 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-43534dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85239944 | |||||
| chr2:85239944
|
TA | T | 172 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0090others(169): Show | 172 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(169): Show |
intron_variant | MODIFIER | c.442-43534delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85239944 | |||||
| chr2:85239958
|
A | C | 4 | a0001c0001t0001g0149a0001c0001t0002g0106a0009c0014t0002g0164others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-43537A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239958 | ||||||
| chr2:85239961
|
AC | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0210a0001c0001t0001g0234others(2): Show | 5 | HG01175.hp2 HG01256.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-43533delC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239961 | ||||||
| chr2:85239962
|
C | A | 16 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(13): Show | 16 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-43533C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239962 | ||||||
| chr2:85240124
|
G | A | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.442-43371G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240124 | ||||||
| chr2:85240316
|
G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-43179G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240316 | ||||||
| chr2:85240335
|
G | T | 2 | a0002c0002t0001g0089a0002c0002t0002g0043 | 2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.442-43160G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240335 | ||||||
| chr2:85240418
|
C | G | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-43077C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240418 | ||||||
| chr2:85240541
|
G | T | 4 | a0001c0001t0001g0210a0002c0002t0002g0018a0003c0003t0002g0086others(1): Show | 4 | HG02572.hp1 HG03225.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-42954G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240541 | ||||||
| chr2:85240551
|
C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-42944C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240551 | ||||||
| chr2:85240617
|
C | CA | 76 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(73): Show | 76 | HG00735.hp1 HG00741.hp2 HG01109.hp1 others(73): Show |
intron_variant | MODIFIER | c.442-42862dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240617 | |||||
| chr2:85240617
|
C | CAA | 9 | a0001c0001t0001g0149a0001c0001t0002g0106a0001c0001t0002g0194others(6): Show | 9 | HG01243.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-42863_442-4286 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240617 | |||||
| chr2:85240732
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(2): Show | 5 | HG03041.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-42763C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240732 | ||||||
| chr2:85240752
|
G | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-42743G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240752 | ||||||
| chr2:85240776
|
C | CA | 42 | a0001c0001t0001g0014a0001c0001t0001g0090a0001c0001t0001g0107others(39): Show | 42 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.442-42700dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240776 | |||||
| chr2:85240776
|
C | CAA | 28 | a0001c0001t0001g0031a0001c0001t0001g0156a0001c0001t0001g0161others(25): Show | 28 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-42701_442-4270 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240776 | |||||
| chr2:85240879
|
G | A | 35 | a0001c0001t0001g0031a0001c0001t0001g0156a0001c0001t0001g0161others(32): Show | 35 | HG01071.hp2 HG01109.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.442-42616G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240879 | ||||||
| chr2:85240933
|
T | G | 5 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-42562T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240933 | ||||||
| chr2:85240995
|
T | A | 2 | a0001c0001t0002g0181a0002c0002t0001g0118 | 2 | NA18959.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.442-42500T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240995 | ||||||
| chr2:85241431
|
G | GTT | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.442-42060_442-4205 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | |||||
| chr2:85241431
|
G | GTTTT | 4 | a0001c0001t0001g0199a0002c0002t0001g0038a0002c0002t0001g0042others(1): Show | 4 | HG01071.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-42062_442-4205 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | |||||
| chr2:85241431
|
G | GTTTTT | 7 | a0001c0001t0001g0156a0002c0002t0001g0024a0002c0002t0001g0040others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-42063_442-4205 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | |||||
| chr2:85241431
|
GTTTTTGT others(3): Show |
G | 12 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0163others(9): Show | 12 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-42058_442-4204 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | |||||
| chr2:85241431
|
GTTTTTGT others(5): Show |
G | 2 | a0001c0001t0002g0104a0002c0002t0001g0051 | 2 | HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-42058_442-4204 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | |||||
| chr2:85241431
|
GTTTTTGT others(6): Show |
G | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(1): Show | 4 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-42058_442-4204 others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | |||||
| chr2:85241437
|
G | GT | 30 | a0001c0001t0001g0076a0001c0001t0001g0095a0001c0001t0001g0099others(27): Show | 30 | HG00597.hp1 HG00621.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.442-42030dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241437 | |||||
| chr2:85241437
|
G | T | 16 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(13): Show | 16 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-42058G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241437 | ||||||
| chr2:85241437
|
GT | G | 9 | a0001c0001t0001g0117a0002c0002t0001g0061a0002c0002t0001g0118others(6): Show | 9 | HG00735.hp1 HG02132.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-42030delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241437 | |||||
| chr2:85241437
|
GTT | G | 46 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(43): Show | 46 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-42031_442-4203 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241437 | |||||
| chr2:85241439
|
T | G | 3 | a0001c0001t0002g0167a0001c0001t0002g0174a0001c0001t0002g0175 | 3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.442-42056T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241439 | ||||||
| chr2:85241443
|
T | G | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-42052T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241443 | ||||||
| chr2:85241448
|
T | G | 4 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059others(1): Show | 4 | HG00735.hp1 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-42047T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241448 | ||||||
| chr2:85241449
|
T | G | 44 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(41): Show | 44 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.442-42046T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241449 | ||||||
| chr2:85241455
|
T | G | 12 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0163others(9): Show | 12 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-42040T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241455 | ||||||
| chr2:85241748
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-41747G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241748 | ||||||
| chr2:85241756
|
T | G | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.442-41739T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241756 | ||||||
| chr2:85241928
|
C | T | 3 | a0001c0001t0001g0210a0003c0003t0002g0086a0005c0012t0002g0184 | 3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.442-41567C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241928 | ||||||
| chr2:85242010
|
G | T | 5 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059others(2): Show | 5 | HG00735.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-41485G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242010 | ||||||
| chr2:85242023
|
C | CG | 180 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(177): Show | 180 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(177): Show |
intron_variant | MODIFIER | c.442-41465dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85242023 | |||||
| chr2:85242123
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0131 | 2 | HG01074.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.442-41372T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242123 | ||||||
| chr2:85242244
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-41251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242244 | ||||||
| chr2:85242244
|
TGG | T | 30 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(27): Show | 30 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.442-41249_442-4124 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85242244 | |||||
| chr2:85242534
|
T | G | 43 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(40): Show | 43 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.442-40961T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242534 | ||||||
| chr2:85242866
|
C | T | 13 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(10): Show | 13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-40629C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242866 | ||||||
| chr2:85242895
|
T | C | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.442-40600T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242895 | ||||||
| chr2:85242964
|
A | G | 131 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(128): Show | 131 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(128): Show |
intron_variant | MODIFIER | c.442-40531A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242964 | ||||||
| chr2:85242974
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-40521A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242974 | ||||||
| chr2:85242982
|
C | T | 47 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(44): Show | 47 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.442-40513C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242982 | ||||||
| chr2:85243040
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-40455C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243040 | ||||||
| chr2:85243158
|
G | A | 26 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0095others(23): Show | 26 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.442-40337G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243158 | ||||||
| chr2:85243179
|
A | G | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-40316A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243179 | ||||||
| chr2:85243276
|
G | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0156a0001c0001t0001g0161others(22): Show | 25 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-40219G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243276 | ||||||
| chr2:85243300
|
C | T | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-40195C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243300 | ||||||
| chr2:85243473
|
AGGGGAAC others(19): Show |
A | 3 | a0001c0001t0002g0104a0002c0002t0001g0050a0002c0002t0001g0051 | 3 | HG01516.hp2 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-40015_442-3999 others(30): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85243473 | |||||
| chr2:85243494
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-40001C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243494 | ||||||
| chr2:85243532
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.442-39963G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243532 | ||||||
| chr2:85243538
|
G | A | 1 | a0002c0002t0001g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.442-39957G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243538 | ||||||
| chr2:85243659
|
C | G | 9 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0002g0189others(6): Show | 9 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-39836C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243659 | ||||||
| chr2:85243799
|
A | G | 25 | a0001c0001t0001g0031a0001c0001t0001g0156a0001c0001t0001g0161others(22): Show | 25 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-39696A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243799 | ||||||
| chr2:85243864
|
A | G | 153 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(150): Show | 153 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(150): Show |
intron_variant | MODIFIER | c.442-39631A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243864 | ||||||
| chr2:85243935
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-39560C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243935 | ||||||
| chr2:85243971
|
A | G | 4 | a0002c0002t0001g0061a0002c0002t0002g0018a0002c0002t0002g0062others(1): Show | 4 | HG00735.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-39524A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243971 | ||||||
| chr2:85244085
|
C | G | 1 | a0011c0017t0001g0220 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442-39410C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244085 | ||||||
| chr2:85244106
|
G | C | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-39389G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244106 | ||||||
| chr2:85244336
|
T | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0097others(56): Show | 59 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.442-39159T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244336 | ||||||
| chr2:85244513
|
G | A | 6 | a0001c0001t0001g0210a0001c0001t0002g0194a0001c0001t0002g0195others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38982G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244513 | ||||||
| chr2:85244516
|
AG | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38978delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244516 | ||||||
| chr2:85244830
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.442-38665C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244830 | ||||||
| chr2:85244837
|
A | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38658A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244837 | ||||||
| chr2:85244853
|
A | G | 14 | a0001c0001t0001g0088a0001c0001t0001g0188a0001c0001t0001g0190others(11): Show | 14 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-38642A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244853 | ||||||
| chr2:85244857
|
G | A | 50 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0107others(47): Show | 50 | HG00741.hp2 HG01168.hp1 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.442-38638G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244857 | ||||||
| chr2:85244932
|
G | A | 39 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0122others(36): Show | 39 | HG00741.hp2 HG01168.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.442-38563G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244932 | ||||||
| chr2:85244965
|
G | A | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-38530G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244965 | ||||||
| chr2:85245039
|
C | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-38456C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245039 | ||||||
| chr2:85245112
|
C | T | 1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442-38383C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245112 | ||||||
| chr2:85245243
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.442-38252A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245243 | ||||||
| chr2:85245244
|
T | C | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-38251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245244 | ||||||
| chr2:85245475
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38020T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245475 | ||||||
| chr2:85245529
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.442-37966C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245529 | ||||||
| chr2:85245833
|
TA | T | 24 | a0001c0001t0001g0117a0001c0001t0001g0193a0001c0001t0001g0199others(21): Show | 24 | HG01071.hp2 HG01109.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.442-37647delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85245833 | |||||
| chr2:85245833
|
TAA | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-37648_442-3764 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85245833 | |||||
| chr2:85245844
|
A | C | 10 | a0001c0001t0001g0090a0002c0002t0001g0007a0002c0002t0001g0010others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-37651A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245844 | ||||||
| chr2:85245846
|
A | C | 2 | a0001c0001t0001g0149a0009c0014t0002g0164 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-37649A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245846 | ||||||
| chr2:85246057
|
AATGC | A | 14 | a0001c0001t0001g0156a0001c0001t0001g0193a0001c0001t0001g0199others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-37436_442-3743 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85246057 | |||||
| chr2:85246137
|
C | A | 121 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(118): Show | 121 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(118): Show |
intron_variant | MODIFIER | c.442-37358C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85246137 | ||||||
| chr2:85246341
|
G | C | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-37154G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85246341 | ||||||
| chr2:85246765
|
AT | A | 37 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-36723delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85246765 | |||||
| chr2:85247075
|
A | C | 2 | a0002c0007t0002g0029a0003c0003t0002g0197 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-36420A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247075 | ||||||
| chr2:85247086
|
C | T | 1 | a0001c0001t0011g0116 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.442-36409C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247086 | ||||||
| chr2:85247123
|
T | C | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-36372T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247123 | ||||||
| chr2:85247160
|
G | A | 37 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0092others(34): Show | 37 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-36335G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247160 | ||||||
| chr2:85247217
|
C | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-36278C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247217 | ||||||
| chr2:85247302
|
C | T | 6 | a0001c0001t0002g0134a0001c0001t0002g0167a0001c0001t0002g0174others(3): Show | 6 | HG01168.hp1 HG02080.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-36193C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247302 | ||||||
| chr2:85247309
|
T | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-36186T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247309 | ||||||
| chr2:85247445
|
A | C | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-36050A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247445 | ||||||
| chr2:85247684
|
G | A | 2 | a0002c0002t0001g0069a0002c0002t0001g0081 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-35811G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247684 | ||||||
| chr2:85247921
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0133 | 2 | NA18953.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.442-35574A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247921 | ||||||
| chr2:85247931
|
C | G | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-35564C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247931 | ||||||
| chr2:85247951
|
C | G | 1 | a0006c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.442-35544C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247951 | ||||||
| chr2:85248274
|
C | T | 46 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0092others(43): Show | 46 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.442-35221C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248274 | ||||||
| chr2:85248580
|
T | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0163others(8): Show | 11 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-34915T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248580 | ||||||
| chr2:85248583
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-34912C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248583 | ||||||
| chr2:85248704
|
T | C | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-34791T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248704 | ||||||
| chr2:85248918
|
C | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-34577C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248918 | ||||||
| chr2:85249000
|
G | GA | 45 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0092others(42): Show | 45 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.442-34485dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85249000 | |||||
| chr2:85249001
|
A | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-34494A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249001 | ||||||
| chr2:85249057
|
T | C | 211 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0076others(208): Show | 211 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.442-34438T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249057 | ||||||
| chr2:85249088
|
T | G | 1 | a0002c0002t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.442-34407T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249088 | ||||||
| chr2:85249129
|
G | A | 2 | a0001c0001t0001g0107a0002c0002t0001g0034 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-34366G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249129 | ||||||
| chr2:85249435
|
G | A | 4 | a0001c0001t0002g0104a0002c0002t0001g0050a0002c0002t0001g0051others(1): Show | 4 | HG01175.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-34060G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249435 | ||||||
| chr2:85249653
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.442-33842C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249653 | ||||||
| chr2:85249758
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442-33737G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249758 | ||||||
| chr2:85250089
|
A | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-33406A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250089 | ||||||
| chr2:85250290
|
A | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-33205A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250290 | ||||||
| chr2:85250403
|
T | A | 2 | a0002c0007t0002g0029a0003c0003t0002g0197 | 2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-33092T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250403 | ||||||
| chr2:85250403
|
T | C | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-33092T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250403 | ||||||
| chr2:85250442
|
A | AT | 45 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0092others(42): Show | 45 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.442-33041dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85250442 | |||||
| chr2:85250579
|
G | A | 2 | a0002c0002t0001g0061a0002c0002t0002g0062 | 2 | HG00735.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-32916G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250579 | ||||||
| chr2:85250594
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-32901G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250594 | ||||||
| chr2:85250597
|
T | C | 135 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(132): Show | 135 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(132): Show |
intron_variant | MODIFIER | c.442-32898T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250597 | ||||||
| chr2:85250716
|
G | T | 2 | a0002c0002t0002g0027a0002c0002t0002g0054 | 2 | HG03491.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.442-32779G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250716 | ||||||
| chr2:85250912
|
A | G | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-32583A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250912 | ||||||
| chr2:85251126
|
T | A | 10 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0001g0163others(7): Show | 10 | HG02572.hp2 HG02717.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-32369T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251126 | ||||||
| chr2:85251146
|
GTTTAC | G | 4 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(1): Show | 4 | HG03041.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-32346_442-3234 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85251146 | |||||
| chr2:85251191
|
G | A | 3 | a0002c0002t0001g0061a0002c0002t0002g0062a0002c0002t0008g0059 | 3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-32304G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251191 | ||||||
| chr2:85251547
|
C | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-31948C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251547 | ||||||
| chr2:85251788
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0223 | 2 | HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.442-31707C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251788 | ||||||
| chr2:85251790
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-31705A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251790 | ||||||
| chr2:85251883
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0006g0005 | 2 | HG00639.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.442-31612G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251883 | ||||||
| chr2:85251886
|
T | C | 235 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(232): Show | 235 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(232): Show |
intron_variant | MODIFIER | c.442-31609T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251886 | ||||||
| chr2:85252007
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-31488C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252007 | ||||||
| chr2:85252101
|
G | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-31394G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252101 | ||||||
| chr2:85252116
|
T | G | 4 | a0001c0001t0002g0098a0001c0001t0002g0194a0001c0001t0002g0195others(1): Show | 4 | HG02258.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-31379T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252116 | ||||||
| chr2:85252117
|
G | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0183a0001c0001t0001g0216others(10): Show | 13 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-31378G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252117 | ||||||
| chr2:85252179
|
T | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-31316T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252179 | ||||||
| chr2:85252369
|
T | G | 1 | a0006c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.442-31126T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252369 | ||||||
| chr2:85252602
|
G | A | 2 | a0001c0001t0001g0149a0009c0014t0002g0164 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-30893G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252602 | ||||||
| chr2:85252603
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-30892C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252603 | ||||||
| chr2:85252825
|
T | G | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0173 | 3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-30670T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252825 | ||||||
| chr2:85252866
|
A | C | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-30629A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252866 | ||||||
| chr2:85252888
|
T | C | 63 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(60): Show | 63 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.442-30607T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252888 | ||||||
| chr2:85252984
|
T | G | 57 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(54): Show | 57 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.442-30511T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252984 | ||||||
| chr2:85253098
|
T | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-30397T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253098 | ||||||
| chr2:85253112
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.442-30383C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253112 | ||||||
| chr2:85253141
|
C | T | 1 | a0002c0002t0002g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.442-30354C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253141 | ||||||
| chr2:85253299
|
T | C | 39 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0149others(36): Show | 39 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.442-30196T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253299 | ||||||
| chr2:85253302
|
G | A | 62 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(59): Show | 62 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.442-30193G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253302 | ||||||
| chr2:85253341
|
A | G | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-30154A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253341 | ||||||
| chr2:85253366
|
G | A | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-30129G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253366 | ||||||
| chr2:85253413
|
G | C | 3 | a0001c0001t0001g0212a0001c0001t0001g0217a0011c0017t0001g0220 | 3 | HG00280.hp1 HG01168.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.442-30082G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253413 | ||||||
| chr2:85253538
|
G | A | 64 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(61): Show | 64 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-29957G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253538 | ||||||
| chr2:85253575
|
T | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-29920T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253575 | ||||||
| chr2:85253592
|
A | G | 58 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(55): Show | 58 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.442-29903A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253592 | ||||||
| chr2:85253694
|
T | G | 64 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(61): Show | 64 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-29801T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253694 | ||||||
| chr2:85254066
|
G | A | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-29429G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254066 | ||||||
| chr2:85254189
|
G | A | 235 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(232): Show | 235 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(232): Show |
intron_variant | MODIFIER | c.442-29306G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254189 | ||||||
| chr2:85254226
|
A | G | 11 | a0001c0001t0001g0090a0001c0001t0002g0189a0001c0001t0002g0202others(8): Show | 11 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-29269A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254226 | ||||||
| chr2:85254276
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-29219G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254276 | ||||||
| chr2:85254302
|
C | T | 1 | a0002c0002t0003g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.442-29193C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254302 | ||||||
| chr2:85254401
|
G | A | 58 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(55): Show | 58 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.442-29094G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254401 | ||||||
| chr2:85254427
|
G | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-29068G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254427 | ||||||
| chr2:85254443
|
C | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0232a0001c0001t0001g0234others(6): Show | 9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-29052C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254443 | ||||||
| chr2:85254495
|
G | A | 2 | a0002c0002t0001g0009a0002c0002t0002g0016 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.442-29000G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254495 | ||||||
| chr2:85254694
|
C | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-28801C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254694 | ||||||
| chr2:85254946
|
G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-28549G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254946 | ||||||
| chr2:85254984
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-28511C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254984 | ||||||
| chr2:85255072
|
T | C | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-28423T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255072 | ||||||
| chr2:85255092
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-28403G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255092 | ||||||
| chr2:85255120
|
G | C | 11 | a0001c0001t0001g0090a0001c0001t0002g0189a0001c0001t0002g0202others(8): Show | 11 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-28375G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255120 | ||||||
| chr2:85255226
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.442-28269C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255226 | ||||||
| chr2:85255246
|
C | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-28249C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255246 | ||||||
| chr2:85255623
|
G | A | 36 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0160others(33): Show | 36 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.442-27872G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255623 | ||||||
| chr2:85255643
|
C | G | 3 | a0001c0001t0001g0149a0002c0002t0004g0085a0009c0014t0002g0164 | 3 | HG02257.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.442-27852C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255643 | ||||||
| chr2:85255880
|
G | A | 118 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(115): Show | 118 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.442-27615G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255880 | ||||||
| chr2:85256022
|
G | A | 40 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0149others(37): Show | 40 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.442-27473G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256022 | ||||||
| chr2:85256118
|
G | A | 2 | a0002c0002t0001g0042a0002c0002t0002g0044 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.442-27377G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256118 | ||||||
| chr2:85256184
|
T | C | 1 | a0005c0005t0009g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.442-27311T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256184 | ||||||
| chr2:85256213
|
C | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.442-27282C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256213 | ||||||
| chr2:85256214
|
G | A | 2 | a0001c0001t0001g0179a0002c0002t0003g0078 | 2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.442-27281G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256214 | ||||||
| chr2:85256227
|
A | T | 103 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(100): Show | 103 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.442-27268A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256227 | ||||||
| chr2:85256258
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-27237G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256258 | ||||||
| chr2:85256273
|
T | C | 17 | a0001c0001t0001g0122a0001c0001t0001g0160a0001c0001t0001g0206others(14): Show | 17 | HG01074.hp2 HG01106.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-27222T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256273 | ||||||
| chr2:85256293
|
G | A | 1 | a0002c0002t0002g0028 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.442-27202G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256293 | ||||||
| chr2:85256566
|
A | G | 4 | a0001c0001t0002g0191a0002c0002t0001g0061a0002c0002t0002g0062others(1): Show | 4 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-26929A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256566 | ||||||
| chr2:85256581
|
G | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(35): Show | 38 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.442-26914G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256581 | ||||||
| chr2:85256686
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0137others(5): Show | 8 | HG01074.hp1 HG01257.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-26809G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256686 | ||||||
| chr2:85256780
|
T | A | 34 | a0001c0001t0001g0090a0001c0001t0001g0099a0001c0001t0001g0128others(31): Show | 34 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-26715T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256780 | ||||||
| chr2:85256783
|
G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-26712G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256783 | ||||||
| chr2:85256812
|
A | G | 2 | a0001c0001t0001g0234a0002c0002t0001g0033 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.442-26683A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256812 | ||||||
| chr2:85256982
|
T | TA | 117 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(114): Show | 117 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.442-26501dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85256982 | |||||
| chr2:85257396
|
G | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0232a0001c0001t0001g0234others(6): Show | 9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-26099G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257396 | ||||||
| chr2:85257643
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-25852G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257643 | ||||||
| chr2:85257655
|
G | GCCCTGCC others(3): Show |
9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-25834_442-2582 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85257655 | |||||
| chr2:85257695
|
G | A | 87 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0088others(84): Show | 87 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.442-25800G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257695 | ||||||
| chr2:85257836
|
C | T | 77 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(74): Show | 77 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-25659C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257836 | ||||||
| chr2:85257899
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.442-25596G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257899 | ||||||
| chr2:85257984
|
T | C | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-25511T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257984 | ||||||
| chr2:85258120
|
G | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-25375G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258120 | ||||||
| chr2:85258139
|
T | C | 1 | a0003c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.442-25356T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258139 | ||||||
| chr2:85258172
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.442-25323C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258172 | ||||||
| chr2:85258203
|
T | C | 27 | a0001c0001t0001g0099a0001c0001t0001g0128a0001c0001t0001g0135others(24): Show | 27 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-25292T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258203 | ||||||
| chr2:85258365
|
C | T | 2 | a0001c0001t0002g0204a0001c0016t0001g0186 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-25130C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258365 | ||||||
| chr2:85258395
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-25100T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258395 | ||||||
| chr2:85258457
|
G | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-25038G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258457 | ||||||
| chr2:85258502
|
A | G | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24993A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258502 | ||||||
| chr2:85258644
|
G | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(5): Show | 8 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-24851G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258644 | ||||||
| chr2:85258783
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.442-24712C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258783 | ||||||
| chr2:85258792
|
G | A | 74 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(71): Show | 74 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.442-24703G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258792 | ||||||
| chr2:85258909
|
C | T | 5 | a0001c0001t0001g0230a0002c0002t0002g0018a0002c0002t0002g0058others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-24586C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258909 | ||||||
| chr2:85259019
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-24476C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259019 | ||||||
| chr2:85259039
|
C | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(6): Show | 9 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-24456C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259039 | ||||||
| chr2:85259069
|
C | G | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24426C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259069 | ||||||
| chr2:85259089
|
T | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-24406T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259089 | ||||||
| chr2:85259107
|
C | T | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24388C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259107 | ||||||
| chr2:85259194
|
G | A | 4 | a0003c0003t0002g0086a0005c0005t0001g0115a0005c0005t0009g0192others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24301G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259194 | ||||||
| chr2:85259231
|
T | G | 160 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(157): Show | 160 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.442-24264T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259231 | ||||||
| chr2:85259262
|
C | T | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24233C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259262 | ||||||
| chr2:85259430
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-24065C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259430 | ||||||
| chr2:85259449
|
A | C | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-24046A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259449 | ||||||
| chr2:85259449
|
A | G | 6 | a0001c0001t0001g0230a0002c0002t0002g0018a0002c0002t0002g0058others(3): Show | 6 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-24046A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259449 | ||||||
| chr2:85259542
|
T | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-23953T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259542 | ||||||
| chr2:85259556
|
A | C | 4 | a0003c0003t0002g0086a0005c0005t0001g0115a0005c0005t0009g0192others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-23939A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259556 | ||||||
| chr2:85259579
|
G | A | 3 | a0001c0001t0002g0104a0002c0002t0001g0050a0002c0002t0001g0051 | 3 | HG01516.hp2 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-23916G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259579 | ||||||
| chr2:85259830
|
T | G | 2 | a0001c0001t0001g0149a0009c0014t0002g0164 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-23665T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259830 | ||||||
| chr2:85259853
|
G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-23642G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259853 | ||||||
| chr2:85259999
|
C | T | 5 | a0001c0001t0001g0097a0001c0001t0001g0177a0001c0001t0001g0196others(2): Show | 5 | HG02523.hp1 NA18747.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-23496C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259999 | ||||||
| chr2:85260033
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.442-23462G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260033 | ||||||
| chr2:85260034
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.442-23461C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260034 | ||||||
| chr2:85260107
|
G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-23388G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260107 | ||||||
| chr2:85260291
|
G | T | 4 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082others(1): Show | 4 | HG02258.hp1 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-23204G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260291 | ||||||
| chr2:85260599
|
G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-22896G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260599 | ||||||
| chr2:85260643
|
C | CA | 73 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(70): Show | 73 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.442-22840dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85260643 | |||||
| chr2:85260716
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-22779C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260716 | ||||||
| chr2:85260761
|
G | A | 12 | a0001c0001t0001g0096a0001c0001t0001g0132a0001c0001t0001g0133others(9): Show | 12 | HG00597.hp2 HG00741.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-22734G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260761 | ||||||
| chr2:85261122
|
T | TGG | 8 | a0001c0001t0001g0102a0001c0001t0001g0120a0001c0001t0001g0180others(5): Show | 8 | HG01074.hp1 HG01168.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-22372_442-2237 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261122 | |||||
| chr2:85261123
|
G | GGT | 27 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0110others(24): Show | 27 | HG00280.hp1 HG00738.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-22324_442-2232 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
G | GGTGT | 8 | a0001c0001t0001g0109a0001c0001t0001g0111a0001c0001t0001g0128others(5): Show | 8 | HG01261.hp1 HG01891.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-22326_442-2232 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
G | GGTGTGT | 5 | a0001c0001t0001g0088a0001c0001t0002g0103a0001c0001t0002g0125others(2): Show | 5 | HG01346.hp2 HG02886.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-22328_442-2232 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
GGT | G | 49 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0101others(46): Show | 49 | HG00639.hp1 HG00639.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.442-22324_442-2232 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
GGTGT | G | 27 | a0001c0001t0001g0090a0001c0001t0001g0149a0001c0001t0001g0155others(24): Show | 27 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-22326_442-2232 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
GGTGTGT | G | 15 | a0001c0001t0001g0091a0001c0001t0001g0140a0001c0001t0001g0200others(12): Show | 15 | HG00597.hp2 HG02080.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-22328_442-2232 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
GGTGTGTG others(1): Show |
G | 15 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(12): Show | 15 | HG00735.hp1 HG01256.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-22330_442-2232 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0001g0015a0001c0001t0002g0106a0002c0002t0003g0077 | 3 | HG02922.hp2 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.442-22332_442-2232 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
GGTGTGTG others(5): Show |
G | 4 | a0001c0001t0002g0194a0001c0001t0002g0195a0002c0002t0001g0034others(1): Show | 4 | HG02258.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-22334_442-2232 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261123
|
GGTGTGTG others(9): Show |
G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-22338_442-2232 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | |||||
| chr2:85261125
|
T | G | 23 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0092others(20): Show | 23 | HG00597.hp1 HG00738.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.442-22370T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261125 | ||||||
| chr2:85261127
|
T | G | 21 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0001g0117others(18): Show | 21 | HG00639.hp1 HG01071.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-22368T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261127 | ||||||
| chr2:85261129
|
T | G | 6 | a0001c0001t0001g0226a0001c0001t0002g0141a0002c0002t0001g0025others(3): Show | 6 | HG00735.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-22366T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261129 | ||||||
| chr2:85261131
|
T | G | 13 | a0001c0001t0001g0091a0001c0001t0001g0200a0001c0001t0001g0222others(10): Show | 13 | HG02080.hp1 HG02080.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-22364T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261131 | ||||||
| chr2:85261133
|
T | G | 5 | a0001c0001t0002g0098a0001c0001t0002g0134a0001c0001t0007g0114others(2): Show | 5 | HG01256.hp1 HG03098.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-22362T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261133 | ||||||
| chr2:85261135
|
T | G | 1 | a0002c0002t0003g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.442-22360T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261135 | ||||||
| chr2:85261141
|
T | G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-22354T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261141 | ||||||
| chr2:85261172
|
G | GTGT | 3 | a0001c0001t0001g0113a0001c0001t0001g0198a0001c0001t0002g0211 | 3 | HG01243.hp1 HG02056.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.442-22323_442-2232 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261172 | ||||||
| chr2:85261328
|
A | T | 75 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(72): Show | 75 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.442-22167A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261328 | ||||||
| chr2:85261410
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0178a0002c0002t0003g0068others(1): Show | 4 | HG01074.hp1 HG01257.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-22085C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261410 | ||||||
| chr2:85261420
|
C | T | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-22075C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261420 | ||||||
| chr2:85261726
|
TA | T | 66 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(63): Show | 66 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.442-21758delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261726 | |||||
| chr2:85261835
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-21660C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261835 | ||||||
| chr2:85261888
|
G | T | 72 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(69): Show | 72 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.442-21607G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261888 | ||||||
| chr2:85262157
|
A | G | 79 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(76): Show | 79 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.442-21338A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262157 | ||||||
| chr2:85262174
|
T | A | 75 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(72): Show | 75 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.442-21321T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262174 | ||||||
| chr2:85262268
|
C | CT | 91 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(88): Show | 91 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.442-21227_442-2122 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262268 | ||||||
| chr2:85262315
|
G | C | 2 | a0001c0001t0001g0209a0002c0002t0004g0055 | 2 | HG02056.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.442-21180G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262315 | ||||||
| chr2:85262392
|
G | GA | 5 | a0001c0001t0001g0230a0001c0001t0002g0204a0001c0016t0001g0186others(2): Show | 5 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-21090dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85262392 | |||||
| chr2:85262392
|
GA | G | 12 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0170others(9): Show | 12 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-21090delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85262392 | |||||
| chr2:85262524
|
A | G | 3 | a0001c0001t0001g0230a0002c0002t0002g0058a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-20971A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262524 | ||||||
| chr2:85262895
|
A | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0196a0001c0001t0001g0198 | 3 | NA18747.hp1 NA18943.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.442-20600A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262895 | ||||||
| chr2:85262989
|
T | A | 55 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(52): Show | 55 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.442-20506T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262989 | ||||||
| chr2:85263044
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-20451G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263044 | ||||||
| chr2:85263170
|
C | T | 1 | a0002c0002t0003g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.442-20325C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263170 | ||||||
| chr2:85263299
|
T | C | 5 | a0001c0001t0001g0230a0002c0002t0002g0058a0002c0002t0004g0085others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-20196T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263299 | ||||||
| chr2:85263319
|
A | AG | 56 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(53): Show | 56 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.442-20169dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85263319 | |||||
| chr2:85263853
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0002g0194a0001c0001t0002g0195others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-19642C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263853 | ||||||
| chr2:85263854
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.442-19641G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263854 | ||||||
| chr2:85263881
|
C | T | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-19614C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263881 | ||||||
| chr2:85264103
|
G | T | 1 | a0002c0002t0003g0079 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.442-19392G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264103 | ||||||
| chr2:85264113
|
A | G | 3 | a0001c0001t0001g0188a0002c0002t0007g0006a0012c0010t0001g0207 | 3 | HG02965.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.442-19382A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264113 | ||||||
| chr2:85264130
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-19365C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264130 | ||||||
| chr2:85264242
|
T | C | 57 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(54): Show | 57 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.442-19253T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264242 | ||||||
| chr2:85264277
|
C | CA | 2 | a0002c0002t0001g0093a0002c0002t0001g0094 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.442-19217dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85264277 | |||||
| chr2:85264297
|
T | C | 89 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(86): Show | 89 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.442-19198T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264297 | ||||||
| chr2:85264551
|
C | T | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-18944C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264551 | ||||||
| chr2:85264559
|
A | G | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-18936A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264559 | ||||||
| chr2:85264624
|
T | C | 63 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(60): Show | 63 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.442-18871T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264624 | ||||||
| chr2:85264647
|
G | A | 89 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(86): Show | 89 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.442-18848G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264647 | ||||||
| chr2:85264744
|
A | ATT | 4 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082others(1): Show | 4 | HG02258.hp1 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-18750_442-1874 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85264744 | |||||
| chr2:85264803
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442-18692C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264803 | ||||||
| chr2:85265018
|
C | T | 90 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(87): Show | 90 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.442-18477C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265018 | ||||||
| chr2:85265032
|
G | A | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-18463G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265032 | ||||||
| chr2:85265268
|
G | T | 89 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(86): Show | 89 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.442-18227G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265268 | ||||||
| chr2:85265292
|
T | TA | 86 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(83): Show | 86 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.442-18190dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85265292 | |||||
| chr2:85265484
|
C | G | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-18011C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265484 | ||||||
| chr2:85265596
|
G | A | 1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-17899G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265596 | ||||||
| chr2:85265766
|
G | GTT | 10 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(7): Show | 10 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-17718_442-1771 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85265766 | |||||
| chr2:85265791
|
A | G | 1 | a0002c0002t0001g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.442-17704A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265791 | ||||||
| chr2:85265879
|
A | C | 89 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(86): Show | 89 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.442-17616A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265879 | ||||||
| chr2:85266197
|
G | A | 1 | a0001c0001t0002g0127 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.442-17298G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266197 | ||||||
| chr2:85266313
|
A | G | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(2): Show | 5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-17182A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266313 | ||||||
| chr2:85266446
|
C | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-17049C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266446 | ||||||
| chr2:85266586
|
T | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-16909T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266586 | ||||||
| chr2:85266596
|
C | T | 2 | a0001c0001t0002g0204a0001c0016t0001g0186 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-16899C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266596 | ||||||
| chr2:85266606
|
C | T | 5 | a0001c0001t0002g0191a0002c0002t0001g0061a0002c0002t0002g0062others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-16889C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266606 | ||||||
| chr2:85266642
|
T | G | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-16853T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266642 | ||||||
| chr2:85266952
|
C | T | 1 | a0008c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.442-16543C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266952 | ||||||
| chr2:85266986
|
G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-16509G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266986 | ||||||
| chr2:85267190
|
A | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-16305A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267190 | ||||||
| chr2:85267198
|
G | A | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-16297G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267198 | ||||||
| chr2:85267263
|
G | A | 47 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0109others(44): Show | 47 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.442-16232G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267263 | ||||||
| chr2:85267292
|
C | T | 5 | a0001c0001t0001g0230a0002c0002t0002g0018a0002c0002t0002g0058others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-16203C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267292 | ||||||
| chr2:85267330
|
C | CA | 15 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0155others(12): Show | 15 | HG01175.hp1 HG02080.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-16142dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267330 | |||||
| chr2:85267330
|
CA | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 11 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-16142delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267330 | |||||
| chr2:85267474
|
C | A | 5 | a0001c0001t0001g0230a0002c0002t0002g0018a0002c0002t0002g0058others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-16021C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267474 | ||||||
| chr2:85267649
|
C | CA | 59 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(56): Show | 59 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.442-15828dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267649 | |||||
| chr2:85267649
|
CA | C | 15 | a0001c0001t0001g0230a0001c0001t0002g0138a0002c0002t0001g0051others(12): Show | 15 | HG01074.hp2 HG01517.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-15828delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267649 | |||||
| chr2:85267760
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-15735C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267760 | ||||||
| chr2:85268135
|
A | G | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-15360A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268135 | ||||||
| chr2:85268213
|
G | T | 4 | a0003c0003t0002g0086a0005c0005t0001g0115a0005c0005t0009g0192others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-15282G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268213 | ||||||
| chr2:85268370
|
G | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-15125G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268370 | ||||||
| chr2:85268471
|
C | CTT | 46 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(43): Show | 46 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.442-15006_442-1500 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268471 | |||||
| chr2:85268471
|
CT | C | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(5): Show | 8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-15005delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268471 | |||||
| chr2:85268472
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0002g0205 | 2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.442-15023T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268472 | ||||||
| chr2:85268536
|
C | T | 16 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0163others(13): Show | 16 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-14959C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268536 | ||||||
| chr2:85268621
|
T | C | 1 | a0002c0002t0003g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.442-14874T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268621 | ||||||
| chr2:85268661
|
C | T | 16 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0163others(13): Show | 16 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-14834C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268661 | ||||||
| chr2:85268712
|
G | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-14783G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268712 | ||||||
| chr2:85268732
|
G | A | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-14763G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268732 | ||||||
| chr2:85268759
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-14736C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268759 | ||||||
| chr2:85268767
|
TA | T | 149 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(146): Show | 149 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.442-14711delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268767 | |||||
| chr2:85268767
|
TAA | T | 10 | a0001c0001t0001g0230a0001c0001t0002g0194a0001c0001t0002g0195others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-14712_442-1471 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268767 | |||||
| chr2:85268808
|
G | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-14687G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268808 | ||||||
| chr2:85268862
|
G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-14633G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268862 | ||||||
| chr2:85268950
|
T | C | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-14545T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268950 | ||||||
| chr2:85268976
|
T | C | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-14519T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268976 | ||||||
| chr2:85269011
|
A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-14484A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269011 | ||||||
| chr2:85269032
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0002g0100 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.442-14463C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269032 | ||||||
| chr2:85269209
|
G | A | 234 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(231): Show | 234 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(231): Show |
intron_variant | MODIFIER | c.442-14286G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269209 | ||||||
| chr2:85269229
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.442-14266G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269229 | ||||||
| chr2:85269401
|
C | T | 5 | a0001c0001t0001g0230a0002c0002t0002g0018a0002c0002t0002g0058others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-14094C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269401 | ||||||
| chr2:85269473
|
A | G | 9 | a0001c0001t0001g0031a0001c0001t0001g0232a0001c0001t0001g0234others(6): Show | 9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-14022A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269473 | ||||||
| chr2:85269587
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-13908C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269587 | ||||||
| chr2:85269716
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.442-13779T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269716 | ||||||
| chr2:85269815
|
G | A | 1 | a0009c0014t0002g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.442-13680G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269815 | ||||||
| chr2:85269838
|
A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-13657A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269838 | ||||||
| chr2:85269881
|
T | C | 9 | a0001c0001t0001g0031a0001c0001t0001g0232a0001c0001t0001g0234others(6): Show | 9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-13614T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269881 | ||||||
| chr2:85269981
|
C | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-13514C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269981 | ||||||
| chr2:85270015
|
C | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.442-13480C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270015 | ||||||
| chr2:85270268
|
C | T | 4 | a0001c0001t0002g0191a0002c0002t0001g0061a0002c0002t0002g0062others(1): Show | 4 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-13227C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270268 | ||||||
| chr2:85270774
|
C | T | 3 | a0001c0001t0002g0189a0002c0002t0001g0037a0002c0002t0003g0084 | 3 | HG01167.hp2 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.442-12721C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270774 | ||||||
| chr2:85270775
|
G | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0152others(5): Show | 8 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-12720G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270775 | ||||||
| chr2:85270777
|
G | A | 78 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(75): Show | 78 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.442-12718G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270777 | ||||||
| chr2:85270781
|
G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-12714G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270781 | ||||||
| chr2:85270933
|
G | T | 2 | a0001c0001t0002g0098a0002c0002t0004g0085 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.442-12562G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270933 | ||||||
| chr2:85271065
|
A | G | 4 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0197others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-12430A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271065 | ||||||
| chr2:85271098
|
G | A | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0003c0003t0002g0082 | 3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-12397G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271098 | ||||||
| chr2:85271253
|
C | T | 2 | a0001c0001t0002g0211a0002c0002t0001g0013 | 2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.442-12242C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271253 | ||||||
| chr2:85271287
|
G | A | 11 | a0001c0001t0001g0230a0001c0001t0002g0098a0002c0002t0002g0018others(8): Show | 11 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-12208G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271287 | ||||||
| chr2:85271370
|
G | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0232a0001c0001t0001g0234others(6): Show | 9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-12125G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271370 | ||||||
| chr2:85271660
|
A | G | 63 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(60): Show | 63 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.442-11835A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271660 | ||||||
| chr2:85271763
|
C | T | 39 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(36): Show | 39 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.442-11732C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271763 | ||||||
| chr2:85271797
|
C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-11698C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271797 | ||||||
| chr2:85271845
|
G | A | 77 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(74): Show | 77 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.442-11650G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271845 | ||||||
| chr2:85272016
|
G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-11479G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272016 | ||||||
| chr2:85272043
|
C | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-11452C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272043 | ||||||
| chr2:85272064
|
C | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-11431C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272064 | ||||||
| chr2:85272070
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.442-11425C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272070 | ||||||
| chr2:85272109
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.442-11386G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272109 | ||||||
| chr2:85272413
|
C | T | 3 | a0001c0001t0002g0106a0001c0001t0002g0194a0001c0001t0002g0195 | 3 | HG02258.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442-11082C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272413 | ||||||
| chr2:85272439
|
C | T | 73 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(70): Show | 73 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.442-11056C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272439 | ||||||
| chr2:85272519
|
G | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(61): Show | 64 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-10976G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272519 | ||||||
| chr2:85272631
|
C | CA | 21 | a0001c0001t0001g0099a0001c0001t0001g0135a0001c0001t0001g0145others(18): Show | 21 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-10850dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85272631 | |||||
| chr2:85272631
|
CA | C | 7 | a0001c0001t0001g0128a0001c0001t0001g0212a0001c0001t0001g0217others(4): Show | 7 | HG00280.hp1 HG01168.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-10850delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85272631 | |||||
| chr2:85272903
|
T | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-10592T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272903 | ||||||
| chr2:85272997
|
A | C | 1 | a0002c0002t0001g0126 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.442-10498A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272997 | ||||||
| chr2:85273020
|
G | A | 1 | a0002c0002t0003g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.442-10475G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273020 | ||||||
| chr2:85273029
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-10466C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273029 | ||||||
| chr2:85273128
|
A | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-10367A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273128 | ||||||
| chr2:85273155
|
A | G | 94 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(91): Show | 94 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.442-10340A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273155 | ||||||
| chr2:85273269
|
A | T | 5 | a0001c0001t0001g0230a0002c0002t0002g0058a0003c0003t0002g0036others(2): Show | 5 | HG02451.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-10226A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273269 | ||||||
| chr2:85273326
|
C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-10169C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273326 | ||||||
| chr2:85273466
|
G | T | 3 | a0001c0001t0001g0107a0002c0002t0001g0089a0002c0002t0002g0043 | 3 | HG01109.hp1 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-10029G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273466 | ||||||
| chr2:85273595
|
T | G | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-9900T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273595 | ||||||
| chr2:85273743
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-9752G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273743 | ||||||
| chr2:85273826
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-9669C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273826 | ||||||
| chr2:85273838
|
G | A | 15 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0163others(12): Show | 15 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-9657G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273838 | ||||||
| chr2:85273950
|
G | A | 71 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(68): Show | 71 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.442-9545G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273950 | ||||||
| chr2:85274031
|
G | A | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-9464G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274031 | ||||||
| chr2:85274058
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442-9437G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274058 | ||||||
| chr2:85274242
|
C | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-9253C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274242 | ||||||
| chr2:85274261
|
C | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(62): Show | 65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-9234C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274261 | ||||||
| chr2:85274267
|
G | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(62): Show | 65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-9228G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274267 | ||||||
| chr2:85274286
|
C | T | 65 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(62): Show | 65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-9209C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274286 | ||||||
| chr2:85274290
|
C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-9205C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274290 | ||||||
| chr2:85274342
|
G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-9153G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274342 | ||||||
| chr2:85274344
|
G | C | 66 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(63): Show | 66 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.442-9151G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274344 | ||||||
| chr2:85274583
|
A | G | 5 | a0003c0003t0002g0082a0003c0003t0002g0086a0005c0005t0001g0115others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8912A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274583 | ||||||
| chr2:85274636
|
G | A | 5 | a0003c0003t0002g0082a0003c0003t0002g0086a0005c0005t0001g0115others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8859G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274636 | ||||||
| chr2:85274876
|
G | A | 66 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(63): Show | 66 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.442-8619G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274876 | ||||||
| chr2:85274908
|
T | G | 5 | a0003c0003t0002g0082a0003c0003t0002g0086a0005c0005t0001g0115others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8587T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274908 | ||||||
| chr2:85275093
|
C | G | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.442-8402C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275093 | ||||||
| chr2:85275113
|
G | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(46): Show | 49 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.442-8382G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275113 | ||||||
| chr2:85275141
|
A | C | 217 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(214): Show | 217 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.442-8354A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275141 | ||||||
| chr2:85275176
|
C | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.442-8319C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275176 | ||||||
| chr2:85275296
|
G | A | 119 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(116): Show | 119 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.442-8199G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275296 | ||||||
| chr2:85275312
|
C | T | 5 | a0003c0003t0002g0082a0003c0003t0002g0086a0005c0005t0001g0115others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8183C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275312 | ||||||
| chr2:85275641
|
G | C | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-7854G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275641 | ||||||
| chr2:85275919
|
C | CA | 39 | a0001c0001t0001g0090a0001c0001t0001g0099a0001c0001t0001g0111others(36): Show | 39 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.442-7558dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | |||||
| chr2:85275919
|
C | CAA | 72 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(69): Show | 72 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.442-7559_442-7558d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | |||||
| chr2:85275919
|
C | CAAA | 65 | a0001c0001t0001g0015a0001c0001t0001g0091a0001c0001t0001g0097others(62): Show | 65 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-7560_442-7558d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | |||||
| chr2:85275919
|
C | CAAAA | 10 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0001g0155others(7): Show | 10 | HG00280.hp1 HG01168.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-7561_442-7558d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | |||||
| chr2:85275938
|
T | A | 28 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0110others(25): Show | 28 | HG00741.hp1 HG01891.hp2 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-7557T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275938 | ||||||
| chr2:85276016
|
G | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(45): Show | 48 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.442-7479G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276016 | ||||||
| chr2:85276070
|
C | G | 6 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0104others(3): Show | 6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-7425C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276070 | ||||||
| chr2:85276289
|
T | C | 3 | a0001c0001t0001g0230a0002c0002t0002g0058a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-7206T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276289 | ||||||
| chr2:85276413
|
G | A | 2 | a0001c0001t0001g0178a0002c0002t0003g0079 | 2 | NA18966.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.442-7082G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276413 | ||||||
| chr2:85276445
|
A | C | 71 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(68): Show | 71 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.442-7050A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276445 | ||||||
| chr2:85276551
|
A | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(61): Show | 64 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-6944A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276551 | ||||||
| chr2:85276588
|
C | T | 3 | a0001c0001t0001g0107a0002c0002t0001g0089a0002c0002t0002g0043 | 3 | HG01109.hp1 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-6907C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276588 | ||||||
| chr2:85276723
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.442-6772A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276723 | ||||||
| chr2:85276873
|
A | G | 155 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(152): Show | 155 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.442-6622A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276873 | ||||||
| chr2:85277068
|
G | A | 64 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(61): Show | 64 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-6427G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277068 | ||||||
| chr2:85277309
|
G | A | 5 | a0003c0003t0002g0082a0003c0003t0002g0086a0005c0005t0001g0115others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-6186G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277309 | ||||||
| chr2:85277372
|
A | G | 2 | a0001c0001t0001g0149a0009c0014t0002g0164 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-6123A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277372 | ||||||
| chr2:85277581
|
G | A | 77 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(74): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-5914G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277581 | ||||||
| chr2:85277743
|
G | T | 15 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0163others(12): Show | 15 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-5752G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277743 | ||||||
| chr2:85277754
|
A | G | 77 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(74): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-5741A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277754 | ||||||
| chr2:85277759
|
A | G | 1 | a0002c0002t0003g0079 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.442-5736A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277759 | ||||||
| chr2:85277827
|
G | A | 2 | a0001c0001t0001g0090a0002c0002t0001g0030 | 2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.442-5668G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277827 | ||||||
| chr2:85277866
|
A | G | 134 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(131): Show | 134 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.442-5629A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277866 | ||||||
| chr2:85277882
|
TAG | T | 3 | a0001c0001t0001g0230a0002c0002t0002g0058a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-5610_442-5609d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85277882 | |||||
| chr2:85277984
|
T | C | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442-5511T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277984 | ||||||
| chr2:85277992
|
C | T | 1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-5503C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277992 | ||||||
| chr2:85278138
|
C | T | 2 | a0001c0001t0001g0179a0002c0002t0003g0078 | 2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.442-5357C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278138 | ||||||
| chr2:85278202
|
C | T | 4 | a0001c0001t0002g0194a0001c0001t0002g0195a0004c0004t0002g0124others(1): Show | 4 | HG02258.hp1 HG02895.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-5293C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278202 | ||||||
| chr2:85278257
|
G | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-5238G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278257 | ||||||
| chr2:85278346
|
G | A | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.442-5149G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278346 | ||||||
| chr2:85278439
|
T | C | 77 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(74): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-5056T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278439 | ||||||
| chr2:85278479
|
C | T | 17 | a0001c0001t0001g0107a0001c0001t0001g0156a0001c0001t0001g0193others(14): Show | 17 | HG01071.hp2 HG01074.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-5016C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278479 | ||||||
| chr2:85278588
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0002g0125a0001c0001t0002g0127others(1): Show | 4 | HG02056.hp1 NA18951.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-4907G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278588 | ||||||
| chr2:85278797
|
C | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(45): Show | 48 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.442-4698C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278797 | ||||||
| chr2:85278857
|
T | A | 77 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(74): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4638T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278857 | ||||||
| chr2:85278877
|
G | A | 77 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(74): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4618G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278877 | ||||||
| chr2:85278915
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.442-4580G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278915 | ||||||
| chr2:85278981
|
G | A | 146 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(143): Show | 146 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.442-4514G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278981 | ||||||
| chr2:85279019
|
C | T | 70 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(67): Show | 70 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.442-4476C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279019 | ||||||
| chr2:85279037
|
G | A | 125 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(122): Show | 125 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.442-4458G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279037 | ||||||
| chr2:85279056
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-4439C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279056 | ||||||
| chr2:85279066
|
GT | G | 15 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0163others(12): Show | 15 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-4428delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279066 | ||||||
| chr2:85279140
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0006g0005 | 2 | HG00639.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.442-4355G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279140 | ||||||
| chr2:85279329
|
C | T | 12 | a0001c0001t0001g0149a0001c0001t0001g0161a0001c0001t0001g0163others(9): Show | 12 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-4166C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279329 | ||||||
| chr2:85279377
|
A | ACGTT | 77 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(74): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4118_442-4117i others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279377 | ||||||
| chr2:85279409
|
AAAAT | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(62): Show | 65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-4074_442-4071d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85279409 | |||||
| chr2:85279465
|
T | C | 77 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(74): Show | 77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4030T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279465 | ||||||
| chr2:85279590
|
C | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(2): Show | 5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-3905C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279590 | ||||||
| chr2:85279668
|
C | T | 5 | a0001c0001t0002g0191a0002c0002t0001g0057a0002c0002t0001g0061others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-3827C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279668 | ||||||
| chr2:85279712
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.442-3783A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279712 | ||||||
| chr2:85279970
|
A | C | 2 | a0003c0003t0002g0036a0003c0003t0002g0197 | 2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.442-3525A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279970 | ||||||
| chr2:85280095
|
A | G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-3400A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280095 | ||||||
| chr2:85280211
|
T | C | 125 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(122): Show | 125 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.442-3284T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280211 | ||||||
| chr2:85280220
|
T | A | 1 | a0001c0001t0001g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.442-3275T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280220 | ||||||
| chr2:85280526
|
G | T | 3 | a0001c0001t0001g0230a0002c0002t0002g0058a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-2969G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280526 | ||||||
| chr2:85280534
|
G | A | 70 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(67): Show | 70 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.442-2961G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280534 | ||||||
| chr2:85280665
|
A | T | 70 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(67): Show | 70 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.442-2830A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280665 | ||||||
| chr2:85280823
|
A | G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-2672A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280823 | ||||||
| chr2:85280942
|
C | A | 79 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0107others(76): Show | 79 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.442-2553C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280942 | ||||||
| chr2:85280991
|
G | A | 3 | a0001c0001t0001g0232a0001c0001t0002g0067a0002c0002t0012g0021 | 3 | HG02451.hp2 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.442-2504G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280991 | ||||||
| chr2:85281020
|
CT | C | 69 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0096others(66): Show | 69 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-2454delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281020 | |||||
| chr2:85281020
|
CTT | C | 11 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0152others(8): Show | 11 | HG01167.hp2 HG01243.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-2455_442-2454d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281020 | |||||
| chr2:85281020
|
CTTT | C | 135 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(132): Show | 135 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.442-2456_442-2454d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281020 | |||||
| chr2:85281134
|
C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-2361C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281134 | ||||||
| chr2:85281147
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-2348C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281147 | ||||||
| chr2:85281180
|
T | C | 152 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0076others(149): Show | 152 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.442-2315T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281180 | ||||||
| chr2:85281213
|
C | A | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.442-2282C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281213 | ||||||
| chr2:85281276
|
T | C | 91 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0097others(88): Show | 91 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.442-2219T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281276 | ||||||
| chr2:85281325
|
A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-2170A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281325 | ||||||
| chr2:85281331
|
T | C | 93 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0097others(90): Show | 93 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.442-2164T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281331 | ||||||
| chr2:85281497
|
T | C | 1 | a0002c0002t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.442-1998T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281497 | ||||||
| chr2:85281702
|
G | A | 99 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0095others(96): Show | 99 | HG00280.hp2 HG00597.hp1 HG00741.hp1 others(96): Show |
intron_variant | MODIFIER | c.442-1793G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281702 | ||||||
| chr2:85281727
|
G | A | 70 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(67): Show | 70 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.442-1768G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281727 | ||||||
| chr2:85281847
|
T | C | 7 | a0001c0001t0001g0132a0001c0001t0001g0153a0001c0001t0002g0181others(4): Show | 7 | HG00741.hp1 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1648T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281847 | ||||||
| chr2:85281932
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-1563T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281932 | ||||||
| chr2:85281989
|
C | CT | 84 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(81): Show | 84 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.442-1497dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281989 | |||||
| chr2:85282334
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-1161C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282334 | ||||||
| chr2:85282416
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.442-1079T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282416 | ||||||
| chr2:85282453
|
A | G | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-1042A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282453 | ||||||
| chr2:85282468
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442-1027G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282468 | ||||||
| chr2:85282541
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-954G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282541 | ||||||
| chr2:85282690
|
G | A | 12 | a0001c0001t0001g0135a0001c0001t0001g0183a0001c0001t0001g0216others(9): Show | 12 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-805G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282690 | ||||||
| chr2:85282794
|
T | TTG | 54 | a0001c0001t0001g0015a0001c0001t0001g0090a0001c0001t0001g0102others(51): Show | 54 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.442-653_442-652dup others(2): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
T | TTGTG | 24 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0091others(21): Show | 24 | HG00738.hp1 HG01074.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.442-655_442-652dup others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
T | TTGTGTG | 18 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0112others(15): Show | 18 | HG00735.hp2 HG01257.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-657_442-652dup others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
T | TTGTGTGT others(1): Show |
22 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0140others(19): Show | 22 | HG00597.hp2 HG00738.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.442-659_442-652dup others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
T | TTGTGTGT others(3): Show |
8 | a0001c0001t0001g0105a0001c0001t0001g0139a0001c0001t0001g0206others(5): Show | 8 | HG01256.hp1 HG02080.hp1 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-661_442-652dup others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0101a0001c0001t0001g0117a0001c0001t0001g0130others(2): Show | 5 | HG03139.hp2 HG03486.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-663_442-652dup others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
T | TTGTGTGT others(7): Show |
3 | a0001c0001t0001g0095a0001c0001t0001g0163a0006c0006t0002g0108 | 3 | HG00597.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.442-665_442-652dup others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTG | T | 13 | a0001c0001t0001g0122a0001c0001t0001g0183a0001c0001t0001g0217others(10): Show | 13 | HG00280.hp1 HG00280.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-653_442-652del others(2): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTG | T | 15 | a0001c0001t0001g0135a0001c0001t0001g0190a0001c0001t0001g0225others(12): Show | 15 | HG00741.hp2 HG01106.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-655_442-652del others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTGTG | T | 4 | a0001c0001t0002g0147a0002c0002t0001g0050a0002c0002t0001g0051others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-657_442-652del others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTGTGT others(1): Show |
T | 17 | a0001c0001t0001g0099a0001c0001t0001g0145a0001c0001t0001g0170others(14): Show | 17 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.442-659_442-652del others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0002g0136 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.442-661_442-652del others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0232a0002c0002t0012g0021 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.442-663_442-652del others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-665_442-652del others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-673_442-652del others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282794
|
TTGTGTGT others(21): Show |
T | 5 | a0003c0003t0002g0082a0003c0003t0002g0086a0005c0005t0001g0115others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-679_442-652del others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | |||||
| chr2:85282895
|
G | A | 76 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(73): Show | 76 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.442-600G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282895 | ||||||
| chr2:85282932
|
A | G | 7 | a0003c0003t0002g0036a0003c0003t0002g0082a0003c0003t0002g0086others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-563A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282932 | ||||||
| chr2:85282970
|
A | G | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(6): Show | 9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-525A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282970 | ||||||
| chr2:85283010
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.442-485C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283010 | ||||||
| chr2:85283102
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-393A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283102 | ||||||
| chr2:85283172
|
C | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(53): Show | 56 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.442-323C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283172 | ||||||
| chr2:85283222
|
G | A | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-273G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283222 | ||||||
| chr2:85283251
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0133 | 2 | NA18953.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.442-244A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283251 | ||||||
| chr2:85283261
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(2): Show | 5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-234C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283261 | ||||||
| chr2:85283265
|
T | TCCC | 35 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0145others(32): Show | 35 | HG00280.hp2 HG02056.hp2 HG02257.hp1 others(32): Show |
intron_variant | MODIFIER | c.442-222_442-220dup others(3): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85283265 | |||||
| chr2:85283265
|
T | TCCCC | 46 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0110others(43): Show | 46 | HG01167.hp2 HG01358.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-223_442-220dup others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85283265 | |||||
| chr2:85283271
|
C | CCCG | 49 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(46): Show | 49 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.442-222_442-221ins others(3): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85283271 | |||||
| chr2:85283271
|
C | CG | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(6): Show | 9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-224_442-223ins others(1): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283271 | ||||||
| chr2:85283274
|
C | G | 1 | a0002c0002t0001g0126 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.442-221C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283274 | ||||||
| chr2:85283277
|
A | G | 56 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(53): Show | 56 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.442-218A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283277 | ||||||
| chr2:85283289
|
G | A | 2 | a0001c0001t0002g0204a0001c0016t0001g0186 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-206G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283289 | ||||||
| chr2:85283302
|
G | A | 48 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(45): Show | 48 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.442-193G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283302 | ||||||
| chr2:85283337
|
A | G | 1 | a0002c0002t0003g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.442-158A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283337 | ||||||
| chr2:85283341
|
G | A | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442-154G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283341 | ||||||
| chr2:85283654
|
A | G | 148 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(145): Show | 148 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.525+76A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283654 | ||||||
| chr2:85283708
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+130G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283708 | ||||||
| chr2:85283802
|
C | T | 1 | a0002c0002t0002g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525+224C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283802 | ||||||
| chr2:85283842
|
A | G | 160 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(157): Show | 160 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.525+264A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283842 | ||||||
| chr2:85283855
|
C | T | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(6): Show | 9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+277C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283855 | ||||||
| chr2:85283859
|
C | T | 2 | a0001c0001t0007g0114a0006c0006t0002g0108 | 2 | HG01256.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.525+281C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283859 | ||||||
| chr2:85283897
|
G | A | 2 | a0001c0001t0002g0204a0001c0016t0001g0186 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525+319G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283897 | ||||||
| chr2:85283898
|
T | C | 92 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(89): Show | 92 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.525+320T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283898 | ||||||
| chr2:85283992
|
C | CTGTTTT | 2 | a0001c0001t0001g0190a0002c0002t0001g0236 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.525+438_525+443dup others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85283992 | |||||
| chr2:85284357
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.525+779C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284357 | ||||||
| chr2:85284454
|
C | G | 2 | a0001c0001t0001g0149a0009c0014t0002g0164 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.525+876C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284454 | ||||||
| chr2:85284471
|
A | G | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(6): Show | 9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+893A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284471 | ||||||
| chr2:85284477
|
A | T | 2 | a0001c0001t0001g0149a0009c0014t0002g0164 | 2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.525+899A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284477 | ||||||
| chr2:85284512
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.525+934A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284512 | ||||||
| chr2:85284514
|
C | A | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.525+936C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284514 | ||||||
| chr2:85284523
|
A | T | 27 | a0001c0001t0001g0088a0001c0001t0001g0096a0001c0001t0001g0110others(24): Show | 27 | HG00741.hp1 HG01891.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.525+945A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284523 | ||||||
| chr2:85284639
|
G | A | 1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.525+1061G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284639 | ||||||
| chr2:85284707
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.525+1129A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284707 | ||||||
| chr2:85284939
|
A | G | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(6): Show | 9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+1361A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284939 | ||||||
| chr2:85284950
|
A | C | 2 | a0001c0001t0001g0234a0002c0002t0001g0033 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.525+1372A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284950 | ||||||
| chr2:85284972
|
G | A | 11 | a0001c0001t0001g0122a0001c0001t0001g0206a0001c0001t0001g0209others(8): Show | 11 | HG02056.hp2 HG02165.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.525+1394G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284972 | ||||||
| chr2:85285016
|
G | A | 4 | a0001c0001t0002g0098a0001c0001t0002g0204a0001c0016t0001g0186others(1): Show | 4 | HG02622.hp2 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+1438G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285016 | ||||||
| chr2:85285032
|
T | G | 2 | a0001c0001t0002g0204a0001c0016t0001g0186 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525+1454T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285032 | ||||||
| chr2:85285101
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.525+1523C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285101 | ||||||
| chr2:85285149
|
T | C | 10 | a0001c0001t0001g0149a0001c0001t0001g0230a0001c0001t0002g0106others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1571T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285149 | ||||||
| chr2:85285165
|
G | A | 5 | a0001c0001t0002g0098a0001c0001t0002g0204a0001c0016t0001g0186others(2): Show | 5 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1587G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285165 | ||||||
| chr2:85285175
|
G | A | 1 | a0002c0002t0001g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.525+1597G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285175 | ||||||
| chr2:85285232
|
C | CA | 10 | a0001c0001t0001g0031a0001c0001t0001g0139a0001c0001t0001g0149others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1666dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85285232 | |||||
| chr2:85285234
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.525+1656A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285234 | ||||||
| chr2:85285363
|
T | C | 10 | a0001c0001t0001g0149a0001c0001t0001g0230a0001c0001t0002g0106others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1785T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285363 | ||||||
| chr2:85285370
|
G | A | 1 | a0004c0004t0002g0142 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.525+1792G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285370 | ||||||
| chr2:85285489
|
T | TG | 10 | a0001c0001t0001g0149a0001c0001t0001g0230a0001c0001t0002g0106others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1912dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85285489 | |||||
| chr2:85285505
|
C | T | 10 | a0001c0001t0001g0149a0001c0001t0001g0230a0001c0001t0002g0106others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1927C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285505 | ||||||
| chr2:85285552
|
T | C | 152 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(149): Show | 152 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.525+1974T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285552 | ||||||
| chr2:85285611
|
C | G | 1 | a0001c0001t0002g0211 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.525+2033C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285611 | ||||||
| chr2:85285684
|
G | A | 6 | a0001c0001t0002g0191a0002c0002t0001g0057a0002c0002t0001g0061others(3): Show | 6 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+2106G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285684 | ||||||
| chr2:85285786
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.525+2208G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285786 | ||||||
| chr2:85285837
|
T | C | 4 | a0001c0001t0002g0106a0001c0001t0002g0194a0001c0001t0002g0195others(1): Show | 4 | HG02258.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+2259T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285837 | ||||||
| chr2:85285838
|
T | G | 152 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0076others(149): Show | 152 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.525+2260T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285838 | ||||||
| chr2:85285844
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0002g0066 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.525+2266C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285844 | ||||||
| chr2:85285856
|
G | T | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(6): Show | 9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+2278G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285856 | ||||||
| chr2:85285901
|
A | G | 10 | a0001c0001t0001g0149a0001c0001t0001g0230a0001c0001t0002g0106others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+2323A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285901 | ||||||
| chr2:85285929
|
C | T | 10 | a0001c0001t0001g0149a0001c0001t0001g0230a0001c0001t0002g0106others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+2351C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285929 | ||||||
| chr2:85285945
|
A | C | 3 | a0001c0001t0001g0230a0002c0002t0002g0058a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525+2367A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285945 | ||||||
| chr2:85286038
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.525+2460A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286038 | ||||||
| chr2:85286041
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.525+2463A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286041 | ||||||
| chr2:85286115
|
C | T | 55 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0091others(52): Show | 55 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.525+2537C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286115 | ||||||
| chr2:85286191
|
C | CA | 17 | a0001c0001t0001g0133a0001c0001t0001g0149a0001c0001t0002g0098others(14): Show | 17 | HG01952.hp1 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.525+2632dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85286191 | |||||
| chr2:85286191
|
CA | C | 5 | a0001c0001t0002g0191a0001c0001t0011g0116a0002c0002t0001g0061others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+2632delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85286191 | |||||
| chr2:85286363
|
C | A | 90 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(87): Show | 90 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.525+2785C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286363 | ||||||
| chr2:85286370
|
A | C | 84 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(81): Show | 84 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.525+2792A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286370 | ||||||
| chr2:85286371
|
C | A | 81 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(78): Show | 81 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.525+2793C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286371 | ||||||
| chr2:85286373
|
A | C | 47 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0096others(44): Show | 47 | HG00741.hp1 HG01891.hp2 HG01952.hp1 others(44): Show |
intron_variant | MODIFIER | c.525+2795A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286373 | ||||||
| chr2:85286374
|
A | AC | 10 | a0001c0001t0001g0149a0001c0001t0002g0106a0002c0002t0001g0057others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+2796_525+2797i others(3): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286374 | ||||||
| chr2:85286379
|
A | G | 3 | a0001c0001t0001g0230a0002c0002t0002g0058a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525+2801A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286379 | ||||||
| chr2:85286387
|
C | A | 3 | a0001c0001t0001g0230a0002c0002t0002g0058a0007c0011t0002g0231 | 3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525+2809C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286387 | ||||||
| chr2:85286582
|
G | A | 1 | a0002c0002t0003g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.525+3004G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286582 | ||||||
| chr2:85286599
|
G | C | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(2): Show | 5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+3021G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286599 | ||||||
| chr2:85286681
|
G | C | 77 | a0001c0001t0001g0031a0001c0001t0001g0088a0001c0001t0001g0090others(74): Show | 77 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.525+3103G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286681 | ||||||
| chr2:85286804
|
A | T | 1 | a0004c0004t0002g0124 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.525+3226A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286804 | ||||||
| chr2:85286935
|
C | T | 4 | a0001c0001t0001g0225a0001c0001t0005g0001a0001c0001t0006g0003others(1): Show | 4 | HG00741.hp2 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+3357C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286935 | ||||||
| chr2:85287001
|
A | G | 25 | a0001c0001t0001g0099a0001c0001t0001g0121a0001c0001t0001g0135others(22): Show | 25 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.525+3423A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287001 | ||||||
| chr2:85287059
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+3481G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287059 | ||||||
| chr2:85287110
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.525+3532C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287110 | ||||||
| chr2:85287139
|
C | T | 9 | a0001c0001t0001g0091a0001c0001t0001g0102a0001c0001t0001g0140others(6): Show | 9 | HG00597.hp2 HG02080.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+3561C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287139 | ||||||
| chr2:85287207
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0223 | 2 | HG02129.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.525+3629C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287207 | ||||||
| chr2:85287228
|
T | A | 1 | a0002c0002t0001g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.525+3650T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287228 | ||||||
| chr2:85287453
|
A | G | 22 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0149others(19): Show | 22 | HG02056.hp2 HG02165.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.525+3875A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287453 | ||||||
| chr2:85287594
|
A | G | 52 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0096others(49): Show | 52 | HG00741.hp1 HG01167.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.525+4016A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287594 | ||||||
| chr2:85287809
|
G | A | 29 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0110others(26): Show | 29 | HG00741.hp1 HG01167.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.525+4231G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287809 | ||||||
| chr2:85288020
|
T | C | 5 | a0003c0003t0002g0082a0003c0003t0002g0086a0005c0005t0001g0115others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+4442T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288020 | ||||||
| chr2:85288415
|
G | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(2): Show | 5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+4837G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288415 | ||||||
| chr2:85288620
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.525+5042T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288620 | ||||||
| chr2:85288653
|
G | A | 1 | a0002c0002t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.525+5075G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288653 | ||||||
| chr2:85288870
|
G | A | 1 | a0002c0002t0001g0056 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.525+5292G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288870 | ||||||
| chr2:85288967
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.525+5389G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288967 | ||||||
| chr2:85289094
|
C | A | 10 | a0001c0001t0001g0170a0001c0001t0001g0171a0002c0002t0001g0050others(7): Show | 10 | HG01106.hp1 HG01175.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+5516C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289094 | ||||||
| chr2:85289194
|
A | G | 19 | a0001c0001t0001g0088a0001c0001t0001g0122a0001c0001t0001g0206others(16): Show | 19 | HG02056.hp2 HG02165.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.525+5616A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289194 | ||||||
| chr2:85289221
|
A | AGT | 25 | a0001c0001t0001g0121a0001c0001t0001g0129a0001c0001t0001g0135others(22): Show | 25 | HG00621.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.525+5674_525+5675d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | |||||
| chr2:85289221
|
A | AGTGT | 49 | a0001c0001t0001g0076a0001c0001t0001g0091a0001c0001t0001g0092others(46): Show | 49 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.525+5672_525+5675d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | |||||
| chr2:85289221
|
A | AGTGTGT | 9 | a0001c0001t0001g0230a0001c0001t0002g0134a0001c0001t0002g0167others(6): Show | 9 | HG01243.hp1 HG02080.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+5670_525+5675d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | |||||
| chr2:85289221
|
A | AGTGTGTG others(1): Show |
4 | a0001c0001t0002g0191a0002c0002t0001g0061a0002c0002t0002g0062others(1): Show | 4 | HG00735.hp1 HG01884.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+5668_525+5675d others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | |||||
| chr2:85289221
|
A | AGTGTGTG others(5): Show |
5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0208others(2): Show | 5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+5664_525+5675d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | |||||
| chr2:85289221
|
AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+5662_525+5675d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | |||||
| chr2:85289457
|
G | T | 2 | a0001c0001t0002g0181a0002c0002t0001g0118 | 2 | NA18959.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.525+5879G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289457 | ||||||
| chr2:85289667
|
G | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.525+6089G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289667 | ||||||
| chr2:85289916
|
C | T | 21 | a0001c0001t0001g0099a0001c0001t0001g0121a0001c0001t0001g0135others(18): Show | 21 | HG00741.hp2 HG01106.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.525+6338C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289916 | ||||||
| chr2:85289918
|
C | T | 1 | a0013c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.525+6340C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289918 | ||||||
| chr2:85289965
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.525+6387C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289965 | ||||||
| chr2:85289967
|
C | G | 78 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0088others(75): Show | 78 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.525+6389C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289967 | ||||||
| chr2:85289976
|
G | GT | 15 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0103others(12): Show | 15 | HG01106.hp1 HG01168.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.525+6413dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289976 | |||||
| chr2:85289976
|
GT | G | 102 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0001g0088others(99): Show | 102 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.525+6413delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289976 | |||||
| chr2:85290071
|
G | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0222a0001c0001t0002g0134others(4): Show | 7 | HG02080.hp1 HG02258.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+6493G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290071 | ||||||
| chr2:85290077
|
A | G | 23 | a0001c0001t0001g0099a0001c0001t0001g0121a0001c0001t0001g0135others(20): Show | 23 | HG00741.hp2 HG01106.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.525+6499A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290077 | ||||||
| chr2:85290169
|
C | T | 89 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(86): Show | 89 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.525+6591C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290169 | ||||||
| chr2:85290263
|
G | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0137others(19): Show | 22 | HG01074.hp1 HG01106.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.525+6685G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290263 | ||||||
| chr2:85290372
|
C | T | 3 | a0002c0002t0001g0069a0002c0002t0001g0081a0002c0002t0004g0085 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.525+6794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290372 | ||||||
| chr2:85290400
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.525+6822T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290400 | ||||||
| chr2:85290430
|
T | A | 31 | a0001c0001t0001g0014a0001c0001t0001g0120a0001c0001t0001g0137others(28): Show | 31 | HG01074.hp1 HG01106.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.525+6852T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290430 | ||||||
| chr2:85290467
|
T | C | 68 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0096others(65): Show | 68 | HG00597.hp2 HG00738.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.525+6889T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290467 | ||||||
| chr2:85290627
|
A | G | 68 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0101others(65): Show | 68 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.525+7049A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290627 | ||||||
| chr2:85290646
|
G | A | 63 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0101others(60): Show | 63 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.525+7068G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290646 | ||||||
| chr2:85290660
|
A | G | 28 | a0001c0001t0001g0107a0001c0001t0001g0149a0001c0001t0001g0161others(25): Show | 28 | HG01074.hp2 HG01109.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.525+7082A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290660 | ||||||
| chr2:85290668
|
C | T | 11 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0179others(8): Show | 11 | HG02129.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+7090C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290668 | ||||||
| chr2:85290691
|
T | G | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.525+7113T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290691 | ||||||
| chr2:85290706
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0011g0116 | 2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.525+7128C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290706 | ||||||
| chr2:85290783
|
G | A | 15 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0170others(12): Show | 15 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.525+7205G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290783 | ||||||
| chr2:85291042
|
C | A | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+7464C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291042 | ||||||
| chr2:85291094
|
T | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0206a0001c0001t0001g0208others(3): Show | 6 | HG02257.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+7516T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291094 | ||||||
| chr2:85291141
|
A | G | 1 | a0001c0001t0005g0001 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.525+7563A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291141 | ||||||
| chr2:85291151
|
C | T | 4 | a0002c0002t0001g0034a0002c0002t0001g0069a0002c0002t0001g0081others(1): Show | 4 | HG02895.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+7573C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291151 | ||||||
| chr2:85291360
|
T | C | 25 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0120others(22): Show | 25 | HG00280.hp2 HG01074.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.525+7782T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291360 | ||||||
| chr2:85291431
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.525+7853A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291431 | ||||||
| chr2:85291493
|
C | T | 1 | a0002c0002t0002g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.525+7915C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291493 | ||||||
| chr2:85291560
|
A | AGTTTTG | 2 | a0001c0001t0001g0183a0003c0003t0002g0036 | 2 | HG02451.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.525+8012_525+8017d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291560 | |||||
| chr2:85291560
|
AGTTTTG | A | 64 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0090others(61): Show | 64 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.525+8012_525+8017d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291560 | |||||
| chr2:85291560
|
AGTTTTGG others(5): Show |
A | 19 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0098others(16): Show | 19 | HG00735.hp1 HG00735.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.525+8006_525+8017d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291560 | |||||
| chr2:85291591
|
G | T | 14 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0098others(11): Show | 14 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+8013G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291591 | ||||||
| chr2:85291725
|
T | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.525+8147T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291725 | ||||||
| chr2:85291954
|
T | C | 15 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0098others(12): Show | 15 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.525+8376T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291954 | ||||||
| chr2:85291982
|
TGGTCATA others(330): Show |
T | 210 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(207): Show | 210 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(207): Show |
intron_variant | MODIFIER | c.525+8421_525+8757d others(2): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291982 | |||||
| chr2:85291993
|
A | AT | 5 | a0001c0001t0001g0212a0001c0001t0002g0166a0002c0002t0001g0173others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+8460dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291993 | |||||
| chr2:85291993
|
A | ATTTTTT | 6 | a0001c0001t0002g0147a0001c0001t0005g0002a0002c0002t0001g0050others(3): Show | 6 | HG01258.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+8455_525+8460d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291993 | |||||
| chr2:85292580
|
C | T | 3 | a0001c0001t0005g0004a0005c0005t0001g0115a0005c0005t0009g0192 | 3 | HG01168.hp1 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.525+9002C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85292580 | ||||||
| chr2:85292717
|
C | A | 6 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+9139C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85292717 | ||||||
| chr2:85293065
|
C | T | 13 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0111others(10): Show | 13 | HG01071.hp1 HG01261.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-9419C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293065 | ||||||
| chr2:85293149
|
A | G | 3 | a0001c0001t0002g0162a0001c0001t0002g0211a0007c0011t0002g0231 | 3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.526-9335A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293149 | ||||||
| chr2:85293415
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.526-9069C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293415 | ||||||
| chr2:85293811
|
A | G | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526-8673A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293811 | ||||||
| chr2:85293922
|
C | T | 2 | a0001c0001t0002g0185a0002c0002t0002g0011 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.526-8562C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293922 | ||||||
| chr2:85293965
|
A | C | 40 | a0001c0001t0001g0190a0001c0001t0001g0218a0001c0001t0001g0230others(37): Show | 40 | HG00280.hp2 HG01168.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.526-8519A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293965 | ||||||
| chr2:85293965
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.526-8519A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293965 | ||||||
| chr2:85293982
|
C | A | 151 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(148): Show | 151 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.526-8502C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293982 | ||||||
| chr2:85294026
|
A | AT | 15 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0002g0125others(12): Show | 15 | HG00738.hp1 HG01175.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.526-8430dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTT | 6 | a0001c0001t0002g0162a0002c0002t0001g0069a0002c0002t0008g0059others(3): Show | 6 | HG02559.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-8435_526-8430d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT | 15 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0001g0139others(12): Show | 15 | HG01261.hp2 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.526-8436_526-8430d others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT others(1): Show |
29 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0091others(26): Show | 29 | HG01074.hp1 HG01109.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.526-8437_526-8430d others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT others(2): Show |
36 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0110others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.526-8438_526-8430d others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT others(3): Show |
12 | a0001c0001t0001g0111a0001c0001t0001g0144a0001c0001t0001g0183others(9): Show | 12 | HG01256.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.526-8439_526-8430d others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0090a0001c0001t0001g0135a0001c0001t0001g0210others(1): Show | 4 | HG02135.hp2 HG03225.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-8440_526-8430d others(13): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0201a0002c0002t0001g0064 | 2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.526-8442_526-8430d others(15): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT others(8): Show |
1 | a0002c0002t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.526-8444_526-8430d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294026
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0219 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.526-8447_526-8430d others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | |||||
| chr2:85294045
|
T | TTTTTTTC | 14 | a0001c0001t0001g0109a0001c0001t0001g0145a0001c0001t0001g0154others(11): Show | 14 | HG00621.hp1 HG01257.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.526-8433_526-8432i others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294045 | |||||
| chr2:85294045
|
T | TTTTTTTT others(1): Show |
43 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0092others(40): Show | 43 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.526-8432_526-8431i others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294045 | |||||
| chr2:85294045
|
T | TTTTTTTT others(2): Show |
5 | a0001c0001t0001g0180a0001c0001t0001g0182a0002c0002t0001g0038others(2): Show | 5 | HG00738.hp2 HG01071.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-8431_526-8430i others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294045 | |||||
| chr2:85294046
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.526-8438T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294046 | ||||||
| chr2:85294048
|
T | C | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-8436T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294048 | ||||||
| chr2:85294071
|
CTGTCGCC others(8): Show |
C | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-8412_526-8398d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294071 | ||||||
| chr2:85294073
|
G | C | 160 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(157): Show | 160 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.526-8411G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294073 | ||||||
| chr2:85294092
|
A | G | 1 | a0002c0002t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.526-8392A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294092 | ||||||
| chr2:85294100
|
G | A | 4 | a0001c0001t0002g0138a0001c0001t0002g0141a0001c0001t0005g0002others(1): Show | 4 | HG01074.hp2 HG01243.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-8384G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294100 | ||||||
| chr2:85294129
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.526-8355C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294129 | ||||||
| chr2:85294130
|
G | A | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526-8354G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294130 | ||||||
| chr2:85294132
|
A | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-8352A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294132 | ||||||
| chr2:85294142
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.526-8342T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294142 | ||||||
| chr2:85294145
|
G | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-8339G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294145 | ||||||
| chr2:85294282
|
C | T | 2 | a0001c0001t0002g0098a0002c0002t0001g0045 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-8202C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294282 | ||||||
| chr2:85294316
|
G | C | 2 | a0001c0016t0001g0186a0005c0005t0001g0115 | 2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.526-8168G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294316 | ||||||
| chr2:85294340
|
A | G | 2 | a0001c0001t0007g0114a0002c0002t0007g0006 | 2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.526-8144A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294340 | ||||||
| chr2:85294400
|
G | A | 155 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(152): Show | 155 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.526-8084G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294400 | ||||||
| chr2:85294400
|
G | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0120others(2): Show | 5 | HG01074.hp1 HG01175.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-8084G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294400 | ||||||
| chr2:85294789
|
T | C | 161 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(158): Show | 161 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.526-7695T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294789 | ||||||
| chr2:85295040
|
T | A | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-7444T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295040 | ||||||
| chr2:85295070
|
C | G | 26 | a0001c0001t0001g0212a0001c0001t0002g0104a0001c0001t0002g0138others(23): Show | 26 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.526-7414C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295070 | ||||||
| chr2:85295111
|
C | A | 1 | a0002c0002t0003g0078 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.526-7373C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295111 | ||||||
| chr2:85295119
|
A | G | 1 | a0006c0006t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.526-7365A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295119 | ||||||
| chr2:85295262
|
C | T | 2 | a0001c0001t0002g0098a0002c0002t0001g0045 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-7222C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295262 | ||||||
| chr2:85295387
|
A | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-7097A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295387 | ||||||
| chr2:85295495
|
C | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0148a0002c0002t0003g0071 | 3 | HG00639.hp2 HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.526-6989C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295495 | ||||||
| chr2:85295775
|
C | CT | 26 | a0001c0001t0001g0076a0001c0001t0001g0121a0001c0001t0001g0170others(23): Show | 26 | HG00741.hp1 HG01167.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.526-6687dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85295775 | |||||
| chr2:85295775
|
C | CTT | 133 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(130): Show | 133 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(130): Show |
intron_variant | MODIFIER | c.526-6688_526-6687d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85295775 | |||||
| chr2:85295775
|
C | CTTT | 30 | a0001c0001t0001g0095a0001c0001t0001g0099a0001c0001t0001g0122others(27): Show | 30 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.526-6689_526-6687d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85295775 | |||||
| chr2:85295803
|
C | A | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6681C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295803 | ||||||
| chr2:85295885
|
C | T | 2 | a0001c0001t0002g0098a0002c0002t0001g0045 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-6599C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295885 | ||||||
| chr2:85296041
|
A | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-6443A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296041 | ||||||
| chr2:85296097
|
G | A | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6387G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296097 | ||||||
| chr2:85296153
|
A | G | 160 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(157): Show | 160 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.526-6331A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296153 | ||||||
| chr2:85296182
|
A | G | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6302A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296182 | ||||||
| chr2:85296353
|
G | A | 160 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(157): Show | 160 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.526-6131G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296353 | ||||||
| chr2:85296418
|
T | G | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6066T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296418 | ||||||
| chr2:85296558
|
G | C | 2 | a0001c0001t0002g0098a0002c0002t0001g0045 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-5926G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296558 | ||||||
| chr2:85297246
|
A | G | 12 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0111others(9): Show | 12 | HG01071.hp1 HG01261.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-5238A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297246 | ||||||
| chr2:85297280
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526-5204C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297280 | ||||||
| chr2:85297322
|
G | A | 2 | a0001c0001t0002g0165a0002c0002t0004g0072 | 2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.526-5162G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297322 | ||||||
| chr2:85297367
|
G | A | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-5117G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297367 | ||||||
| chr2:85297545
|
G | T | 5 | a0001c0001t0001g0208a0002c0002t0001g0007a0002c0002t0001g0012others(2): Show | 5 | HG02145.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-4939G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297545 | ||||||
| chr2:85297551
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526-4933C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297551 | ||||||
| chr2:85297635
|
G | A | 1 | a0002c0002t0001g0061 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526-4849G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297635 | ||||||
| chr2:85297699
|
C | T | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-4785C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297699 | ||||||
| chr2:85297726
|
A | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-4758A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297726 | ||||||
| chr2:85297753
|
C | T | 155 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(152): Show | 155 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.526-4731C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297753 | ||||||
| chr2:85297895
|
T | C | 1 | a0002c0002t0001g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.526-4589T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297895 | ||||||
| chr2:85297901
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.526-4583G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297901 | ||||||
| chr2:85297912
|
C | T | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-4572C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297912 | ||||||
| chr2:85297996
|
C | T | 6 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-4488C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297996 | ||||||
| chr2:85298026
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.526-4458C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298026 | ||||||
| chr2:85298083
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.526-4401G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298083 | ||||||
| chr2:85298191
|
C | CAAAA | 6 | a0001c0001t0001g0107a0001c0001t0002g0125a0001c0001t0002g0136others(3): Show | 6 | HG01109.hp1 HG01168.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-4281_526-4278d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298191
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0120a0001c0001t0001g0156 | 2 | HG01074.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.526-4287_526-4278d others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298191
|
C | CAAAAAAA others(4): Show |
44 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0096others(41): Show | 44 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.526-4288_526-4278d others(13): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298191
|
C | CAAAAAAA others(5): Show |
49 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(46): Show | 49 | HG00621.hp2 HG01109.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.526-4289_526-4278d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298191
|
C | CAAAAAAA others(6): Show |
77 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0092others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.526-4290_526-4278d others(15): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298191
|
C | CAAAAAAA others(7): Show |
16 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0154others(13): Show | 16 | HG01106.hp2 HG01934.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.526-4291_526-4278d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298191
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0002g0191a0001c0001t0002g0202a0004c0004t0002g0142others(1): Show | 4 | HG00735.hp2 HG01884.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-4292_526-4278d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298191
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0002g0106a0004c0004t0002g0123a0009c0014t0002g0164 | 3 | HG02148.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.526-4278_526-4277i others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | |||||
| chr2:85298216
|
G | A | 152 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(149): Show | 152 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.526-4268G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298216 | ||||||
| chr2:85298218
|
G | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-4266G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298218 | ||||||
| chr2:85298221
|
C | T | 4 | a0001c0001t0002g0098a0001c0001t0007g0114a0002c0002t0001g0045others(1): Show | 4 | HG01256.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-4263C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298221 | ||||||
| chr2:85298223
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.526-4261G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298223 | ||||||
| chr2:85298350
|
G | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0229 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526-4134G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298350 | ||||||
| chr2:85298367
|
C | T | 187 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(184): Show | 187 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.526-4117C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298367 | ||||||
| chr2:85298481
|
C | CA | 22 | a0001c0001t0001g0088a0001c0001t0001g0144a0001c0001t0001g0156others(19): Show | 22 | HG01168.hp2 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-3982dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | |||||
| chr2:85298481
|
C | CAA | 20 | a0001c0001t0001g0107a0001c0001t0002g0125a0001c0001t0002g0136others(17): Show | 20 | HG00280.hp2 HG01168.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.526-3983_526-3982d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | |||||
| chr2:85298481
|
C | CAAA | 6 | a0001c0001t0001g0218a0001c0001t0001g0230a0002c0002t0001g0030others(3): Show | 6 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-3984_526-3982d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | |||||
| chr2:85298481
|
CA | C | 59 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0092others(56): Show | 59 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.526-3982delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | |||||
| chr2:85298499
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.526-3985A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298499 | ||||||
| chr2:85298500
|
AAAG | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(2): Show | 5 | HG00735.hp1 HG00735.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-3983_526-3981d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298500 | ||||||
| chr2:85298587
|
A | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-3897A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298587 | ||||||
| chr2:85298699
|
GGC | G | 19 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0002g0125others(16): Show | 19 | HG00280.hp2 HG01975.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.526-3784_526-3783d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298699 | ||||||
| chr2:85298875
|
C | G | 1 | a0010c0015t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.526-3609C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298875 | ||||||
| chr2:85298907
|
C | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0137a0001c0001t0001g0216others(2): Show | 5 | HG02135.hp1 NA18951.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-3577C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298907 | ||||||
| chr2:85298918
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.526-3566C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298918 | ||||||
| chr2:85299111
|
A | G | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.526-3373A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299111 | ||||||
| chr2:85299276
|
G | A | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-3208G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299276 | ||||||
| chr2:85299386
|
CTA | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0222a0001c0001t0006g0003 | 3 | HG01516.hp1 HG02258.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.526-3097_526-3096d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299386 | ||||||
| chr2:85299455
|
G | A | 6 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(3): Show | 6 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-3029G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299455 | ||||||
| chr2:85299492
|
CA | C | 48 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0090others(45): Show | 48 | HG00621.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.526-2991delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299492 | ||||||
| chr2:85299576
|
G | A | 1 | a0005c0005t0009g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.526-2908G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299576 | ||||||
| chr2:85299683
|
A | G | 22 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0002g0125others(19): Show | 22 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-2801A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299683 | ||||||
| chr2:85299790
|
T | C | 187 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(184): Show | 187 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.526-2694T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299790 | ||||||
| chr2:85299846
|
G | A | 1 | a0006c0006t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.526-2638G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299846 | ||||||
| chr2:85299860
|
A | AAC | 5 | a0001c0001t0002g0147a0002c0002t0002g0028a0002c0002t0002g0046others(2): Show | 5 | HG00738.hp1 HG01168.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2581_526-2580d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACAC | 4 | a0001c0001t0001g0151a0001c0001t0001g0212a0004c0004t0002g0123others(1): Show | 4 | HG00735.hp2 HG01109.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-2583_526-2580d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(1): Show |
5 | a0001c0001t0001g0121a0002c0002t0002g0018a0002c0002t0002g0066others(2): Show | 5 | HG02723.hp1 HG03491.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-2587_526-2580d others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(3): Show |
1 | a0002c0002t0001g0064 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.526-2589_526-2580d others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(5): Show |
4 | a0001c0001t0001g0219a0001c0001t0002g0103a0002c0002t0001g0040others(1): Show | 4 | HG01071.hp1 HG01346.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-2591_526-2580d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(7): Show |
8 | a0001c0001t0001g0160a0001c0001t0001g0179a0001c0001t0001g0209others(5): Show | 8 | HG01256.hp1 HG01891.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.526-2593_526-2580d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(9): Show |
5 | a0001c0001t0001g0135a0001c0001t0001g0201a0002c0002t0001g0032others(2): Show | 5 | HG01261.hp1 HG02135.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2595_526-2580d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(11): Show |
14 | a0001c0001t0001g0096a0001c0001t0001g0130a0001c0001t0001g0139others(11): Show | 14 | HG00621.hp1 HG00738.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.526-2597_526-2580d others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(13): Show |
11 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(8): Show | 11 | HG00280.hp1 HG01257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.526-2599_526-2580d others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(15): Show |
19 | a0001c0001t0001g0014a0001c0001t0001g0090a0001c0001t0001g0091others(16): Show | 19 | HG00597.hp1 HG00597.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.526-2601_526-2580d others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(17): Show |
28 | a0001c0001t0001g0109a0001c0001t0001g0131a0001c0001t0001g0145others(25): Show | 28 | HG00280.hp2 HG00741.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.526-2603_526-2580d others(26): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(19): Show |
24 | a0001c0001t0001g0076a0001c0001t0001g0102a0001c0001t0001g0107others(21): Show | 24 | HG00621.hp2 HG00639.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-2605_526-2580d others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(21): Show |
11 | a0001c0001t0001g0092a0001c0001t0001g0133a0001c0001t0001g0153others(8): Show | 11 | HG01175.hp1 HG01516.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-2607_526-2580d others(30): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(23): Show |
13 | a0001c0001t0001g0015a0001c0001t0001g0097a0001c0001t0001g0117others(10): Show | 13 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-2609_526-2580d others(32): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(25): Show |
11 | a0001c0001t0001g0113a0001c0001t0001g0152a0001c0001t0001g0178others(8): Show | 11 | HG01981.hp1 HG02056.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-2611_526-2580d others(34): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(27): Show |
5 | a0001c0001t0001g0101a0001c0001t0001g0216a0001c0001t0002g0127others(2): Show | 5 | HG06807.hp1 NA18906.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-2613_526-2580d others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(29): Show |
4 | a0001c0001t0001g0112a0001c0001t0002g0175a0002c0002t0001g0089others(1): Show | 4 | HG01109.hp1 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-2615_526-2580d others(38): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(33): Show |
2 | a0001c0001t0001g0198a0002c0002t0002g0058 | 2 | HG02717.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.526-2619_526-2580d others(42): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | AACACACA others(37): Show |
2 | a0002c0002t0001g0052a0002c0002t0002g0017 | 2 | HG03017.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.526-2623_526-2580d others(46): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.526-2624_526-2623i others(19): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | ||||||
| chr2:85299860
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0002g0159 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.526-2624_526-2623i others(21): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | ||||||
| chr2:85299860
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.526-2624_526-2623i others(23): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | ||||||
| chr2:85299860
|
A | ACACACAC others(22): Show |
5 | a0001c0001t0001g0105a0001c0001t0001g0227a0001c0001t0002g0174others(2): Show | 5 | HG02083.hp2 HG03139.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-2624_526-2623i others(31): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | ||||||
| chr2:85299860
|
A | ACACACAC others(26): Show |
2 | a0001c0001t0001g0144a0001c0001t0002g0119 | 2 | NA18967.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.526-2624_526-2623i others(35): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | ||||||
| chr2:85299860
|
A | ACACACAC others(28): Show |
1 | a0001c0001t0002g0167 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-2624_526-2623i others(37): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | ||||||
| chr2:85299860
|
AAC | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(2): Show | 5 | HG01106.hp1 HG01358.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2581_526-2580d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
AACAC | A | 3 | a0001c0001t0002g0191a0001c0001t0002g0202a0009c0014t0002g0164 | 3 | HG01884.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.526-2583_526-2580d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
AACACACA others(5): Show |
A | 1 | a0005c0005t0009g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.526-2591_526-2580d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
AACACACA others(7): Show |
A | 5 | a0001c0016t0001g0186a0002c0002t0002g0043a0002c0002t0004g0085others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2593_526-2580d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299860
|
AACACACA others(9): Show |
A | 13 | a0001c0001t0001g0088a0001c0001t0001g0190a0001c0001t0002g0067others(10): Show | 13 | HG01168.hp1 HG01261.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-2595_526-2580d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | |||||
| chr2:85299949
|
C | T | 1 | a0008c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.526-2535C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299949 | ||||||
| chr2:85299955
|
G | A | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-2529G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299955 | ||||||
| chr2:85299973
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.526-2511C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299973 | ||||||
| chr2:85300166
|
A | G | 6 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0189others(3): Show | 6 | HG01167.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-2318A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300166 | ||||||
| chr2:85300261
|
T | C | 1 | a0003c0003t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526-2223T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300261 | ||||||
| chr2:85300328
|
T | C | 23 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0002g0125others(20): Show | 23 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.526-2156T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300328 | ||||||
| chr2:85300434
|
A | T | 22 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0002g0125others(19): Show | 22 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-2050A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300434 | ||||||
| chr2:85300463
|
G | T | 32 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0218others(29): Show | 32 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.526-2021G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300463 | ||||||
| chr2:85300578
|
C | T | 23 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0002g0125others(20): Show | 23 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.526-1906C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300578 | ||||||
| chr2:85300649
|
G | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0222a0001c0001t0006g0003 | 3 | HG01516.hp1 HG02258.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.526-1835G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300649 | ||||||
| chr2:85300738
|
G | T | 12 | a0001c0001t0001g0088a0001c0001t0001g0190a0001c0001t0002g0067others(9): Show | 12 | HG01261.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-1746G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300738 | ||||||
| chr2:85300783
|
C | CT | 13 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(10): Show | 13 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-1687dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85300783 | |||||
| chr2:85300851
|
C | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1633C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300851 | ||||||
| chr2:85300946
|
A | C | 1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.526-1538A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300946 | ||||||
| chr2:85300999
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0187 | 2 | HG02080.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.526-1485C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300999 | ||||||
| chr2:85301086
|
C | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1398C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301086 | ||||||
| chr2:85301123
|
ACTTAT | A | 4 | a0001c0001t0002g0098a0001c0001t0007g0114a0002c0002t0001g0045others(1): Show | 4 | HG01256.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-1355_526-1351d others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85301123 | |||||
| chr2:85301128
|
T | C | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1356T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301128 | ||||||
| chr2:85301132
|
A | T | 1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1352A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301132 | ||||||
| chr2:85301146
|
T | C | 10 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-1338T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301146 | ||||||
| chr2:85301172
|
A | G | 1 | a0001c0001t0002g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.526-1312A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301172 | ||||||
| chr2:85301184
|
T | A | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.526-1300T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301184 | ||||||
| chr2:85301261
|
G | A | 9 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(6): Show | 9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-1223G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301261 | ||||||
| chr2:85301520
|
A | G | 10 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-964A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301520 | ||||||
| chr2:85301572
|
T | TTTTC | 10 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-910_526-907dup others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85301572 | |||||
| chr2:85301681
|
A | C | 1 | a0011c0017t0001g0220 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.526-803A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301681 | ||||||
| chr2:85301719
|
G | A | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.526-765G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301719 | ||||||
| chr2:85301784
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.526-700A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301784 | ||||||
| chr2:85301861
|
C | T | 1 | a0001c0001t0007g0114 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.526-623C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301861 | ||||||
| chr2:85301896
|
C | T | 1 | a0001c0001t0006g0005 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.526-588C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301896 | ||||||
| chr2:85301897
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.526-587G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301897 | ||||||
| chr2:85301967
|
A | C | 2 | a0002c0002t0001g0009a0002c0002t0001g0087 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.526-517A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301967 | ||||||
| chr2:85302144
|
C | CA | 9 | a0001c0001t0001g0120a0001c0001t0001g0151a0001c0001t0001g0155others(6): Show | 9 | HG01074.hp1 HG01109.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-330dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85302144 | |||||
| chr2:85302658
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.658+42C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302658 | ||||||
| chr2:85302717
|
C | T | 2 | a0001c0001t0002g0185a0002c0002t0002g0011 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.658+101C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302717 | ||||||
| chr2:85302858
|
A | G | 156 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(153): Show | 156 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.658+242A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302858 | ||||||
| chr2:85302904
|
T | C | 22 | a0001c0001t0001g0218a0001c0001t0001g0230a0001c0001t0002g0125others(19): Show | 22 | HG00280.hp2 HG01243.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.658+288T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302904 | ||||||
| chr2:85302942
|
T | C | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.658+326T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302942 | ||||||
| chr2:85302943
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.658+327G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302943 | ||||||
| chr2:85302994
|
C | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.658+378C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302994 | ||||||
| chr2:85303270
|
C | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.659-625C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303270 | ||||||
| chr2:85303276
|
G | A | 30 | a0001c0001t0001g0088a0001c0001t0001g0161a0001c0001t0001g0163others(27): Show | 30 | HG00735.hp1 HG00735.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.659-619G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303276 | ||||||
| chr2:85303295
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.659-600G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303295 | ||||||
| chr2:85303304
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.659-591G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303304 | ||||||
| chr2:85303438
|
A | G | 209 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(206): Show | 209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.659-457A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303438 | ||||||
| chr2:85303540
|
G | A | 3 | a0001c0001t0002g0162a0001c0001t0002g0211a0007c0011t0002g0231 | 3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.659-355G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303540 | ||||||
| chr2:85303553
|
T | C | 10 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(7): Show | 10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.659-342T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303553 | ||||||
| chr2:85303673
|
G | A | 1 | a0002c0002t0001g0056 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.659-222G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303673 | ||||||
| chr2:85304128
|
A | G | 15 | a0001c0001t0001g0088a0001c0001t0001g0190a0001c0001t0002g0067others(12): Show | 15 | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.762-127A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 6/11 | chr2 | 85304128 | ||||||
| chr2:85304373
|
T | C | 2 | a0002c0002t0001g0118a0002c0002t0003g0080 | 2 | HG02132.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.845+35T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304373 | ||||||
| chr2:85304445
|
C | G | 2 | a0002c0002t0002g0018a0002c0002t0002g0066 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.845+107C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304445 | ||||||
| chr2:85304456
|
C | A | 73 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0092others(70): Show | 73 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.845+118C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304456 | ||||||
| chr2:85304667
|
T | C | 6 | a0001c0001t0002g0138a0001c0001t0002g0141a0001c0001t0002g0166others(3): Show | 6 | HG01074.hp2 HG01243.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.845+329T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304667 | ||||||
| chr2:85304684
|
C | A | 212 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(209): Show | 212 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(209): Show |
intron_variant | MODIFIER | c.845+346C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304684 | ||||||
| chr2:85304795
|
T | C | 16 | a0001c0001t0001g0088a0001c0001t0001g0190a0001c0001t0002g0067others(13): Show | 16 | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.845+457T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304795 | ||||||
| chr2:85304803
|
G | A | 2 | a0001c0001t0007g0114a0002c0002t0007g0006 | 2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.846-457G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304803 | ||||||
| chr2:85304808
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.846-452G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304808 | ||||||
| chr2:85304988
|
C | T | 2 | a0001c0001t0007g0114a0002c0002t0007g0006 | 2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.846-272C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304988 | ||||||
| chr2:85304999
|
C | A | 3 | a0001c0001t0002g0162a0001c0001t0002g0211a0007c0011t0002g0231 | 3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.846-261C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304999 | ||||||
| chr2:85305082
|
C | G | 213 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(210): Show | 213 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.846-178C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85305082 | ||||||
| chr2:85305147
|
T | C | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.846-113T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85305147 | ||||||
| chr2:85305457
|
G | A | 1 | a0004c0004t0002g0123 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.989+54G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305457 | ||||||
| chr2:85305462
|
C | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0226others(1): Show | 4 | HG01346.hp1 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.989+59C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305462 | ||||||
| chr2:85305478
|
A | C | 1 | a0006c0006t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.989+75A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305478 | ||||||
| chr2:85305689
|
G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.989+286G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305689 | ||||||
| chr2:85305745
|
G | C | 2 | a0001c0001t0002g0098a0002c0002t0008g0059 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.989+342G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305745 | ||||||
| chr2:85305862
|
C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.990-344C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305862 | ||||||
| chr2:85305909
|
C | T | 1 | a0002c0002t0003g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.990-297C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305909 | ||||||
| chr2:85306039
|
G | A | 1 | a0006c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.990-167G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85306039 | ||||||
| chr2:85306104
|
G | A | 18 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(15): Show | 18 | HG01071.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.990-102G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85306104 | ||||||
| chr2:85306448
|
C | G | 18 | a0001c0001t0001g0088a0001c0001t0001g0190a0001c0001t0002g0067others(15): Show | 18 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.1150-4C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 9/11 | chr2 | 85306448 | ||||||
| chr2:85306719
|
C | T | 13 | a0001c0001t0001g0088a0001c0001t0001g0190a0001c0001t0002g0067others(10): Show | 13 | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1257+160C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306719 | ||||||
| chr2:85306734
|
G | A | 5 | a0001c0001t0002g0185a0002c0002t0002g0011a0002c0002t0002g0016others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+175G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306734 | ||||||
| chr2:85306864
|
CTG | C | 2 | a0002c0002t0001g0009a0002c0002t0001g0087 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1257+309_1257+310d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 85306864 | |||||
| chr2:85306881
|
G | T | 5 | a0001c0001t0002g0191a0001c0001t0002g0202a0002c0002t0004g0085others(2): Show | 5 | HG01884.hp1 HG02257.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+322G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306881 | ||||||
| chr2:85306900
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0002g0134 | 2 | NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1257+341G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306900 | ||||||
| chr2:85306916
|
G | A | 21 | a0001c0001t0001g0099a0001c0001t0001g0145a0001c0001t0001g0218others(18): Show | 21 | HG00280.hp2 HG01167.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1257+357G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306916 | ||||||
| chr2:85307080
|
G | T | 15 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(12): Show | 15 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1257+521G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307080 | ||||||
| chr2:85307119
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1258-523A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307119 | ||||||
| chr2:85307173
|
T | TAACCC | 148 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0031others(145): Show | 148 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1258-467_1258-463d others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 85307173 | |||||
| chr2:85307192
|
C | T | 5 | a0001c0001t0002g0067a0001c0001t0002g0157a0001c0001t0005g0001others(2): Show | 5 | HG01261.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-450C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307192 | ||||||
| chr2:85307214
|
G | A | 3 | a0001c0016t0001g0186a0005c0005t0001g0115a0005c0005t0009g0192 | 3 | HG02615.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1258-428G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307214 | ||||||
| chr2:85307243
|
A | G | 8 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(5): Show | 8 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1258-399A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307243 | ||||||
| chr2:85307269
|
T | C | 44 | a0001c0001t0001g0088a0001c0001t0001g0161a0001c0001t0001g0163others(41): Show | 44 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-373T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307269 | ||||||
| chr2:85307390
|
G | C | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1258-252G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307390 | ||||||
| chr2:85307406
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1258-236T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307406 | ||||||
| chr2:85307444
|
G | A | 9 | a0001c0001t0002g0134a0001c0001t0002g0147a0001c0001t0002g0165others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1258-198G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307444 | ||||||
| chr2:85307446
|
G | A | 28 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(25): Show | 28 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1258-196G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307446 | ||||||
| chr2:85307451
|
T | C | 44 | a0001c0001t0001g0088a0001c0001t0001g0161a0001c0001t0001g0163others(41): Show | 44 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-191T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307451 | ||||||
| chr2:85307574
|
C | T | 3 | a0001c0001t0002g0162a0001c0001t0002g0211a0007c0011t0002g0231 | 3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1258-68C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307574 | ||||||
| chr2:85307820
|
G | A | 3 | a0001c0001t0002g0162a0001c0001t0002g0211a0007c0011t0002g0231 | 3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1333+103G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85307820 | ||||||
| chr2:85307827
|
G | A | 21 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0002g0106others(18): Show | 21 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1333+110G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85307827 | ||||||
| chr2:85307887
|
G | C | 1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1333+170G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85307887 | ||||||
| chr2:85308064
|
C | T | 11 | a0001c0001t0002g0134a0001c0001t0002g0147a0001c0001t0002g0165others(8): Show | 11 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1333+347C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308064 | ||||||
| chr2:85308099
|
C | T | 3 | a0001c0001t0002g0191a0001c0001t0002g0202a0009c0014t0002g0164 | 3 | HG01884.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1333+382C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308099 | ||||||
| chr2:85308163
|
GCA | G | 2 | a0001c0001t0007g0114a0002c0002t0007g0006 | 2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1333+448_1333+449d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308163 | |||||
| chr2:85308178
|
A | T | 7 | a0001c0001t0001g0149a0001c0001t0001g0208a0002c0002t0001g0007others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1333+461A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308178 | ||||||
| chr2:85308180
|
C | T | 1 | a0006c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1333+463C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308180 | ||||||
| chr2:85308181
|
A | G | 39 | a0001c0001t0001g0088a0001c0001t0001g0161a0001c0001t0001g0163others(36): Show | 39 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1333+464A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308181 | ||||||
| chr2:85308197
|
T | C | 14 | a0001c0001t0001g0088a0001c0001t0001g0190a0001c0001t0002g0191others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333+480T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308197 | ||||||
| chr2:85308246
|
T | C | 7 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(4): Show | 7 | HG01257.hp2 HG01934.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1333+529T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308246 | ||||||
| chr2:85308290
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1333+573A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308290 | ||||||
| chr2:85308314
|
C | T | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1333+597C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308314 | ||||||
| chr2:85308376
|
C | CCATTCTC others(101): Show |
1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1334-652_1334-651i others(110): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308376 | |||||
| chr2:85308376
|
C | CCATTCTC others(81): Show |
10 | a0001c0001t0002g0134a0001c0001t0002g0147a0001c0001t0002g0165others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1334-652_1334-651i others(90): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308376 | |||||
| chr2:85308382
|
A | ACCTTCCC others(29): Show |
1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(38): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | |||||
| chr2:85308382
|
A | ACCTTCCC others(76): Show |
58 | a0001c0001t0001g0031a0001c0001t0001g0090a0001c0001t0001g0091others(55): Show | 58 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(85): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | |||||
| chr2:85308382
|
A | ACCTTCCC others(96): Show |
3 | a0001c0001t0001g0144a0001c0001t0001g0151a0002c0002t0004g0085 | 3 | HG01109.hp2 NA18522.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(105): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | |||||
| chr2:85308382
|
A | ACCTTCCC others(317): Show |
1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(326): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | |||||
| chr2:85308382
|
A | ACCTTCCC others(77): Show |
2 | a0002c0002t0001g0022a0002c0002t0001g0023 | 2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1334-587_1334-586i others(86): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | |||||
| chr2:85308382
|
A | T | 13 | a0001c0001t0001g0122a0001c0001t0001g0130a0001c0001t0002g0134others(10): Show | 13 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1334-647A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308382 | ||||||
| chr2:85308385
|
T | TTCCCTCC others(108): Show |
2 | a0001c0001t0002g0158a0001c0001t0002g0159 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(117): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(341): Show |
2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(350): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(81): Show |
1 | a0003c0003t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(90): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(61): Show |
5 | a0001c0001t0002g0067a0001c0001t0002g0157a0001c0001t0005g0001others(2): Show | 5 | HG01261.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(70): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(133): Show |
1 | a0003c0003t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(142): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(77): Show |
29 | a0001c0001t0001g0099a0001c0001t0001g0145a0001c0001t0001g0177others(26): Show | 29 | HG00280.hp2 HG01074.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(86): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(175): Show |
3 | a0001c0001t0001g0088a0001c0001t0001g0190a0013c0009t0001g0019 | 3 | HG02886.hp2 HG02895.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(184): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(357): Show |
2 | a0002c0002t0001g0069a0002c0002t0001g0081 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(366): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308385
|
T | TTCCCTCC others(57): Show |
7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0189others(4): Show | 7 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(66): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | |||||
| chr2:85308401
|
T | TTCCCTCC others(68): Show |
1 | a0005c0005t0009g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1334-613_1334-612i others(77): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308401 | |||||
| chr2:85308401
|
T | TTCCCTCC others(73): Show |
1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(82): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308401 | |||||
| chr2:85308409
|
C | CTTTCCCC others(73): Show |
2 | a0001c0001t0002g0185a0006c0006t0010g0233 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(82): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308409 | |||||
| chr2:85308409
|
C | CTTTCCCC others(73): Show |
3 | a0001c0001t0002g0119a0001c0001t0002g0127a0005c0012t0002g0184 | 3 | NA18951.hp1 NA19011.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(82): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308409 | |||||
| chr2:85308414
|
C | CCCCTCCC others(163): Show |
2 | a0001c0001t0002g0202a0009c0014t0002g0164 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(172): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308414 | |||||
| chr2:85308414
|
C | CCCCTCCC others(309): Show |
1 | a0001c0001t0002g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(318): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308414 | |||||
| chr2:85308417
|
T | C | 134 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0001g0091others(131): Show | 134 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.1334-612T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308417 | ||||||
| chr2:85308417
|
T | TTCCCTCC others(96): Show |
1 | a0010c0015t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1334-601_1334-600i others(105): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308417 | |||||
| chr2:85308417
|
T | TTCCCTCC others(161): Show |
1 | a0001c0001t0002g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1334-587_1334-586i others(170): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308417 | |||||
| chr2:85308417
|
T | TTCCCTCC others(33): Show |
7 | a0001c0001t0001g0230a0002c0002t0001g0009a0002c0002t0001g0030others(4): Show | 7 | HG02109.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334-586_1334-585i others(42): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308417 | |||||
| chr2:85308433
|
C | CTCCCTCC others(9): Show |
1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1334-586_1334-571d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308433 | |||||
| chr2:85308442
|
TTTCTCTT others(7): Show |
T | 1 | a0002c0002t0002g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1334-586_1334-573d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308442 | ||||||
| chr2:85308444
|
T | C | 2 | a0001c0016t0001g0186a0005c0005t0001g0115 | 2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1334-585T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308444 | ||||||
| chr2:85308447
|
C | G | 142 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0088others(139): Show | 142 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.1334-582C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308447 | ||||||
| chr2:85308447
|
C | T | 2 | a0001c0016t0001g0186a0005c0005t0001g0115 | 2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1334-582C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308447 | ||||||
| chr2:85308449
|
T | C | 2 | a0001c0016t0001g0186a0005c0005t0001g0115 | 2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1334-580T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308449 | ||||||
| chr2:85308456
|
CCT | C | 92 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0090others(89): Show | 92 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.1334-568_1334-567d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308456 | |||||
| chr2:85308457
|
C | CTCCCTCC others(161): Show |
1 | a0005c0005t0001g0115 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1334-570_1334-569i others(170): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | |||||
| chr2:85308457
|
C | CTCCCTCC others(15): Show |
1 | a0001c0016t0001g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1334-570_1334-569i others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | |||||
| chr2:85308457
|
C | CTT | 14 | a0001c0001t0001g0230a0001c0001t0002g0185a0002c0002t0001g0009others(11): Show | 14 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1334-571_1334-570i others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | |||||
| chr2:85308457
|
C | CTTTCTCT others(27): Show |
1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1334-571_1334-570i others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | |||||
| chr2:85308483
|
T | C | 11 | a0001c0001t0001g0090a0001c0001t0001g0149a0001c0001t0001g0193others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1334-546T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308483 | ||||||
| chr2:85308491
|
C | T | 11 | a0001c0001t0001g0090a0001c0001t0001g0149a0001c0001t0001g0193others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1334-538C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308491 | ||||||
| chr2:85308493
|
TC | T | 25 | a0001c0001t0001g0088a0001c0001t0001g0179a0001c0001t0001g0201others(22): Show | 25 | HG00639.hp1 HG00741.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1334-529delC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308493 | |||||
| chr2:85308793
|
G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1334-236G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308793 | ||||||
| chr2:85308903
|
G | A | 2 | a0001c0001t0001g0140a0002c0002t0003g0075 | 2 | HG00597.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1334-126G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308903 | ||||||
| chr2:85308919
|
G | A | 2 | a0002c0002t0008g0059a0005c0005t0009g0192 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1334-110G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308919 | ||||||
| chr2:85308982
|
T | C | 5 | a0001c0001t0002g0098a0001c0001t0002g0119a0001c0001t0002g0127others(2): Show | 5 | HG02647.hp1 HG03098.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-47T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308982 | ||||||
| chr2:85309005
|
CTCTT | C | 2 | a0001c0001t0007g0114a0002c0002t0007g0006 | 2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1334-19_1334-16del others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85309005 |