Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6934 |
|---|---|
| ensemblid | ENSG00000148737.18 |
| hgncid | 11641 |
| symbol | TCF7L2 |
| name | transcription factor 7 like 2 |
| refseq_nuc | NM_001367943.1 |
| refseq_prot | NP_001354872.1 |
| ensembl_nuc | ENST00000355995.9 |
| ensembl_prot | ENSP00000348274.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 112950247 |
| end | 113167678 |
| strand | + |
| ver | v1.2 |
| region | chr10:112950247-113167678 |
| region5000 | chr10:112945247-113172678 |
| regionname0 | TCF7L2_chr10_112950247_113167678 |
| regionname5000 | TCF7L2_chr10_112945247_113172678 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 619 | 175 | 79 | 47 | 20 | 9 | 18 | 10 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002 | 0/0 | 619 | 13 | 0 | 2 | 8 | 0 | 3 | 5 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0003 | 0/0 | 619 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0004 | 0/0 | 619 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0005 | 0/0 | 619 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0006 | 0/0 | 619 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0007 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0008 | 0/0 | 619 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0009 | 0/0 | 619 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1860 | 166 | 73 | 45 | 20 | 9 | 17 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0002 | 0/0 | 1860 | 13 | 0 | 2 | 8 | 0 | 3 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0003 | 0/0 | 1860 | 5 | 4 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0004 | 0/0 | 1860 | 4 | 3 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0005 | 0/0 | 1860 | 3 | 3 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0006 | 0/0 | 1860 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0007 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0009 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0010 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0011 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0012 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| c0013 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| 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 | 2218 | 56 | 18 | 10 | 20 | 0 | 8 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0002 | 0/0 | 2217 | 23 | 8 | 10 | 1 | 4 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0003 | 0/0 | 2218 | 11 | 1 | 7 | 2 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0004 | 0/0 | 2218 | 10 | 9 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0005 | 1/0 | 2217 | 10 | 1 | 4 | 0 | 1 | 3 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0006 | 0/0 | 2217 | 10 | 9 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0007 | 0/0 | 2218 | 7 | 0 | 1 | 3 | 0 | 3 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0008 | 0/0 | 2217 | 6 | 6 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0009 | 0/0 | 2218 | 5 | 1 | 2 | 0 | 2 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0010 | 0/0 | 2216 | 5 | 3 | 1 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0011 | 0/0 | 2218 | 5 | 4 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0012 | 0/1 | 2217 | 5 | 0 | 2 | 0 | 1 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0013 | 0/0 | 2217 | 5 | 4 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0014 | 0/0 | 2217 | 3 | 3 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0015 | 0/0 | 2217 | 3 | 1 | 0 | 0 | 0 | 2 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0016 | 0/0 | 2218 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0017 | 0/0 | 2218 | 2 | 0 | 2 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0018 | 0/0 | 2218 | 2 | 0 | 0 | 1 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0019 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0020 | 0/0 | 2218 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0021 | 0/0 | 2218 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0022 | 0/0 | 2218 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0023 | 0/0 | 2218 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0024 | 0/0 | 2218 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0025 | 0/0 | 2218 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0026 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0027 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0028 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0029 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0030 | 0/0 | 2216 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0031 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0032 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0033 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0034 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0035 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0036 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0037 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0038 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0039 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0040 | 0/0 | 2217 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0041 | 0/0 | 2218 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0042 | 0/0 | 2218 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0043 | 0/0 | 2218 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0044 | 0/0 | 2218 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0045 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0046 | 0/0 | 2216 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| t0047 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| 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 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1860 | 166 | 73 | 45 | 20 | 9 | 17 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0004 | 0/0 | 1860 | 4 | 3 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0005 | 0/0 | 1860 | 3 | 3 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0011 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0013 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002c0002 | 0/0 | 1860 | 13 | 0 | 2 | 8 | 0 | 3 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0003c0003 | 0/0 | 1860 | 5 | 4 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0004c0006 | 0/0 | 1860 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0005c0010 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0006c0012 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0007c0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0008c0009 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0009c0007 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4077 | 47 | 16 | 10 | 15 | 0 | 6 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0002 | 0/0 | 4076 | 21 | 7 | 10 | 1 | 3 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0003 | 0/0 | 4077 | 8 | 1 | 6 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0004 | 0/0 | 4077 | 9 | 9 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0005 | 1/0 | 4076 | 9 | 1 | 3 | 0 | 1 | 3 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0006 | 0/0 | 4076 | 9 | 8 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0007 | 0/0 | 4077 | 4 | 0 | 1 | 1 | 0 | 2 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0008 | 0/0 | 4076 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0009 | 0/0 | 4077 | 5 | 1 | 2 | 0 | 2 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0010 | 0/0 | 4075 | 4 | 3 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0011 | 0/0 | 4077 | 4 | 3 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0012 | 0/1 | 4076 | 5 | 0 | 2 | 0 | 1 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0013 | 0/0 | 4076 | 3 | 3 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0014 | 0/0 | 4076 | 3 | 3 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0015 | 0/0 | 4076 | 3 | 1 | 0 | 0 | 0 | 2 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0016 | 0/0 | 4077 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0017 | 0/0 | 4077 | 2 | 0 | 2 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0018 | 0/0 | 4077 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0022 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0023 | 0/0 | 4077 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0024 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0025 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0026 | 0/0 | 4078 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0028 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0029 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0030 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0031 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0033 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0034 | 0/0 | 4076 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0036 | 0/0 | 4076 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0037 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0038 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0039 | 0/0 | 4076 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0040 | 0/0 | 4076 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0041 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0042 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0043 | 0/0 | 4077 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0044 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0045 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0046 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0001t0047 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0004t0008 | 0/0 | 4076 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0004t0013 | 0/0 | 4076 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0005t0006 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0005t0019 | 0/0 | 4076 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0011t0035 | 0/0 | 4076 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0001c0013t0027 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002c0002t0001 | 0/0 | 4077 | 6 | 0 | 0 | 4 | 0 | 2 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002c0002t0003 | 0/0 | 4077 | 2 | 0 | 1 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002c0002t0005 | 0/0 | 4076 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002c0002t0007 | 0/0 | 4077 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002c0002t0010 | 0/0 | 4075 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0002c0002t0018 | 0/0 | 4077 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0003c0003t0004 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0003c0003t0011 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0003c0003t0020 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0003c0003t0021 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0003c0003t0032 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0004c0006t0001 | 0/0 | 4077 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0005c0010t0003 | 0/0 | 4077 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0006c0012t0007 | 0/0 | 4077 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0007c0008t0002 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0008c0009t0002 | 0/0 | 4076 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| a0009c0007t0001 | 0/0 | 4077 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | copy fasta | chr10 | 112945247 | 113172678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0009g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0010g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0010g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0011g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0012g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0012g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0012g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0013g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0013g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0015g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0015g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0016g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0016g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0017g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0017g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0018g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0022g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0023g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0024g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0025g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0026g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0028g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0029g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0030g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0031g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0033g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0034g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0036g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0037g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0038g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0039g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0040g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0041g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0042g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0043g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0044g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0045g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0046g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0001t0047g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0004t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0004t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0004t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0004t0013g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0005t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0005t0019g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0005t0019g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0011t0035g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0001c0013t0027g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0010g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0002c0002t0018g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0003c0003t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0003c0003t0011g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0003c0003t0020g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0003c0003t0021g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0003c0003t0032g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0004c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0004c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0005c0010t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0006c0012t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0007c0008t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0008c0009t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| a0009c0007t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0009 | g0073 | EUR | GBR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0065 | EUR | GBR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00140 | hp1 | a0008 | c0009 | t0002 | g0105 | EUR | GBR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | GBR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0045 | EUR | FIN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00280 | hp2 | a0001 | c0001 | t0012 | g0178 | EUR | FIN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | FIN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00323 | hp2 | a0001 | c0001 | t0043 | g0168 | EUR | FIN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CHS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0085 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00741 | hp1 | a0001 | c0001 | t0012 | g0169 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01070 | hp2 | a0001 | c0001 | t0025 | g0035 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01071 | hp1 | a0001 | c0001 | t0017 | g0052 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01081 | hp1 | a0001 | c0001 | t0011 | g0175 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01081 | hp2 | a0002 | c0002 | t0005 | g0043 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01099 | hp2 | a0001 | c0013 | t0027 | g0037 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0081 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0072 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01109 | hp1 | a0003 | c0003 | t0004 | g0084 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01109 | hp2 | a0001 | c0004 | t0013 | g0147 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01175 | hp2 | a0001 | c0001 | t0044 | g0070 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0188 | AMR | PUR | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01255 | hp1 | a0001 | c0001 | t0040 | g0164 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01358 | hp1 | a0001 | c0001 | t0009 | g0057 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01358 | hp2 | a0001 | c0001 | t0022 | g0050 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0111 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01496 | hp2 | a0001 | c0001 | t0034 | g0187 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01943 | hp1 | a0001 | c0001 | t0017 | g0071 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01978 | hp2 | a0002 | c0002 | t0003 | g0171 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02040 | hp1 | a0002 | c0002 | t0007 | g0198 | EAS | KHV | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02040 | hp2 | a0005 | c0010 | t0003 | g0167 | EAS | KHV | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0151 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02145 | hp2 | a0001 | c0001 | t0026 | g0124 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02165 | hp1 | a0001 | c0001 | t0016 | g0023 | EAS | CDX | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0032 | EAS | CDX | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02257 | hp1 | a0001 | c0001 | t0046 | g0152 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02257 | hp2 | a0004 | c0006 | t0001 | g0039 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02280 | hp1 | a0003 | c0003 | t0020 | g0135 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0103 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02293 | hp1 | a0001 | c0001 | t0041 | g0180 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02300 | hp1 | a0001 | c0001 | t0012 | g0183 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0159 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0083 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02630 | hp1 | a0004 | c0006 | t0001 | g0053 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02647 | hp2 | a0001 | c0001 | t0029 | g0114 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02717 | hp2 | a0003 | c0003 | t0032 | g0011 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02723 | hp1 | a0001 | c0001 | t0042 | g0177 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0165 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0199 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02809 | hp1 | a0001 | c0001 | t0015 | g0008 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0093 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02895 | hp2 | a0001 | c0004 | t0013 | g0145 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02896 | hp2 | a0001 | c0005 | t0019 | g0002 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0092 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02897 | hp2 | a0001 | c0005 | t0019 | g0001 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02922 | hp1 | a0001 | c0001 | t0024 | g0121 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0144 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02965 | hp1 | a0001 | c0001 | t0033 | g0003 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02970 | hp2 | a0007 | c0008 | t0002 | g0015 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03017 | hp1 | a0001 | c0001 | t0023 | g0027 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03017 | hp2 | a0001 | c0011 | t0035 | g0110 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03041 | hp1 | a0001 | c0004 | t0008 | g0146 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03041 | hp2 | a0001 | c0001 | t0031 | g0010 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03098 | hp1 | a0003 | c0003 | t0011 | g0009 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0098 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03139 | hp1 | a0001 | c0001 | t0037 | g0160 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0055 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03195 | hp2 | a0001 | c0001 | t0047 | g0150 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0184 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03516 | hp1 | a0001 | c0001 | t0030 | g0004 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | GWD | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0020 | SAS | PJL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03831 | hp1 | a0001 | c0001 | t0018 | g0069 | SAS | BEB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03831 | hp2 | a0002 | c0002 | t0010 | g0109 | SAS | BEB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0033 | SAS | BEB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03942 | hp2 | a0001 | c0001 | t0036 | g0116 | SAS | BEB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0192 | SAS | STU | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0189 | SAS | STU | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG04199 | hp1 | a0001 | c0001 | t0015 | g0112 | SAS | STU | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0064 | SAS | STU | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG04228 | hp1 | a0006 | c0012 | t0007 | g0026 | SAS | STU | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG04228 | hp2 | a0001 | c0001 | t0015 | g0091 | SAS | STU | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18522 | hp1 | a0003 | c0003 | t0021 | g0120 | AFR | YRI | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0176 | AFR | YRI | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | YRI | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18906 | hp2 | a0001 | c0005 | t0006 | g0138 | AFR | YRI | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18964 | hp1 | a0002 | c0002 | t0007 | g0030 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA18964 | hp2 | a0001 | c0001 | t0016 | g0024 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19010 | hp2 | a0002 | c0002 | t0018 | g0022 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | LWK | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0148 | AFR | LWK | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | LWK | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19063 | hp1 | a0009 | c0007 | t0001 | g0025 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19066 | hp2 | a0001 | c0001 | t0039 | g0166 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19070 | hp1 | a0002 | c0002 | t0003 | g0162 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ASW | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0140 | AFR | ASW | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0122 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0067 | AMR | CLM | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02109 | hp2 | a0001 | c0001 | t0045 | g0156 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0185 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0127 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0153 | AFR | ACB | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03471 | hp1 | a0001 | c0001 | t0028 | g0014 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA20300 | hp2 | a0001 | c0001 | t0038 | g0106 | AFR | USA | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0119 | AFR | LWK | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0080 | AFR | LWK | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0012 | g0154 | REF | REF | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0077 | REF | REF | TCF7L2_chr10_112945247_113172678 | TCF7L2 | chr10 | 112945247 | 113172678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:113151123
|
C | T | 1 | a0005 | 1 | HG02040.hp2 | missense_variant&splice_region_variant | MODERATE | c.1001C>T | p.Ser334Leu | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 9/15 | 1511/4076 | 1001/1860 | 334/619 | chr10 | 113151123 | ||
| chr10:113165610
|
C | A | 1 | a0002 | 13 | HG00597.hp1 HG00597.hp2 HG01081.hp2 others(10): Show |
missense_variant | MODERATE | c.1498C>A | p.Pro500Thr | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 2008/4076 | 1498/1860 | 500/619 | chr10 | 113165610 | ||
| chr10:113165646
|
C | G | 1 | a0006 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1534C>G | p.Pro512Ala | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 2044/4076 | 1534/1860 | 512/619 | chr10 | 113165646 | ||
| chr10:113165647
|
C | A | 1 | a0004 | 2 | HG02257.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.1535C>A | p.Pro512His | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 2045/4076 | 1535/1860 | 512/619 | chr10 | 113165647 | ||
| chr10:113165682
|
G | A | 1 | a0009 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1570G>A | p.Ala524Thr | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 2080/4076 | 1570/1860 | 524/619 | chr10 | 113165682 | ||
| chr10:113165773
|
C | T | 1 | a0008 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1661C>T | p.Ala554Val | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 2171/4076 | 1661/1860 | 554/619 | chr10 | 113165773 | ||
| chr10:113165847
|
G | A | 1 | a0007 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1735G>A | p.Ala579Thr | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 2245/4076 | 1735/1860 | 579/619 | chr10 | 113165847 | ||
| chr10:113165916
|
T | C | 1 | a0003 | 5 | HG01109.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.1804T>C | p.Ser602Pro | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 2314/4076 | 1804/1860 | 602/619 | chr10 | 113165916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:112950766
|
C | T | 1 | a0001c0005 | 3 | HG02896.hp2 HG02897.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.10C>T | p.Leu4Leu | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 520/4076 | 10/1860 | 4/619 | chr10 | 112950766 | ||
| chr10:112950801
|
C | T | 1 | a0001c0004 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.45C>T | p.Asn15Asn | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 555/4076 | 45/1860 | 15/619 | chr10 | 112950801 | ||
| chr10:112951574
|
C | T | 1 | a0001c0013 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.348C>T | p.Leu116Leu | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/15 | 858/4076 | 348/1860 | 116/619 | chr10 | 112951574 | ||
| chr10:113151070
|
A | G | 2 | a0001c0011a0006c0012 | 2 | HG03017.hp2 HG04228.hp1 |
synonymous_variant | LOW | c.948A>G | p.Thr316Thr | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 9/15 | 1458/4076 | 948/1860 | 316/619 | chr10 | 113151070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:112950260
|
G | T | 6 | a0001c0001t0008a0001c0001t0013a0001c0001t0046others(3): Show | 13 | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-497G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 497 | chr10 | 112950260 | |||||
| chr10:112950284
|
G | T | 1 | a0001c0001t0045 | 1 | HG02109.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-473G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | chr10 | 112950284 | ||||||
| chr10:112950299
|
T | G | 1 | a0001c0001t0016 | 2 | HG02165.hp1 NA18964.hp2 |
5_prime_UTR_variant | MODIFIER | c.-458T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 458 | chr10 | 112950299 | |||||
| chr10:112950403
|
TC | T | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(35): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
5_prime_UTR_variant | MODIFIER | c.-345delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 345 | INFO_REALIGN_3_PRIME | chr10 | 112950403 | ||||
| chr10:112950409
|
C | G | 1 | a0001c0001t0044 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-348C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 348 | chr10 | 112950409 | |||||
| chr10:112950449
|
G | GT | 14 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(11): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-294dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 293 | INFO_REALIGN_3_PRIME | chr10 | 112950449 | ||||
| chr10:112950463
|
T | A | 1 | a0003c0003t0020 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-294T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 294 | chr10 | 112950463 | |||||
| chr10:112950464
|
A | C | 1 | a0003c0003t0020 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-293A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 293 | chr10 | 112950464 | |||||
| chr10:112950470
|
C | T | 1 | a0003c0003t0020 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 287 | chr10 | 112950470 | |||||
| chr10:112950666
|
G | T | 1 | a0001c0005t0019 | 2 | HG02896.hp2 HG02897.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | chr10 | 112950666 | ||||||
| chr10:112950673
|
C | G | 1 | a0003c0003t0020 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 84 | chr10 | 112950673 | |||||
| chr10:112950674
|
A | C | 1 | a0003c0003t0020 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-83A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/15 | 83 | chr10 | 112950674 | |||||
| chr10:113165991
|
C | A | 1 | a0001c0001t0028 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 19 | chr10 | 113165991 | |||||
| chr10:113165999
|
T | C | 21 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(18): Show | 47 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*27T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 27 | chr10 | 113165999 | |||||
| chr10:113166036
|
C | T | 1 | a0001c0001t0033 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 64 | chr10 | 113166036 | |||||
| chr10:113166217
|
G | C | 1 | a0001c0001t0029 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 245 | chr10 | 113166217 | |||||
| chr10:113166451
|
C | CT | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*494dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 495 | INFO_REALIGN_3_PRIME | chr10 | 113166451 | ||||
| chr10:113166554
|
T | G | 1 | a0001c0001t0047 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*582T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 582 | chr10 | 113166554 | |||||
| chr10:113166571
|
T | C | 1 | a0001c0001t0022 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 599 | chr10 | 113166571 | |||||
| chr10:113166574
|
G | C | 3 | a0001c0001t0017a0001c0001t0034a0001c0001t0041 | 4 | HG01071.hp1 HG01496.hp2 HG01943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*602G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 602 | chr10 | 113166574 | |||||
| chr10:113166614
|
G | C | 3 | a0001c0001t0018a0001c0011t0035a0002c0002t0018 | 3 | HG03017.hp2 HG03831.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*642G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 642 | chr10 | 113166614 | |||||
| chr10:113166696
|
T | C | 3 | a0001c0001t0009a0001c0001t0023a0001c0001t0036 | 7 | HG00099.hp1 HG00280.hp1 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*724T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 724 | chr10 | 113166696 | |||||
| chr10:113166988
|
T | C | 2 | a0001c0001t0031a0001c0001t0042 | 2 | HG02723.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1016T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1016 | chr10 | 113166988 | |||||
| chr10:113167031
|
C | T | 6 | a0001c0001t0007a0001c0001t0015a0001c0001t0022others(3): Show | 12 | HG00735.hp2 HG01358.hp2 HG02040.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1059C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1059 | chr10 | 113167031 | |||||
| chr10:113167032
|
G | A | 1 | a0001c0001t0039 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1060G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1060 | chr10 | 113167032 | |||||
| chr10:113167043
|
C | T | 1 | a0001c0001t0025 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1071 | chr10 | 113167043 | |||||
| chr10:113167074
|
C | G | 3 | a0001c0001t0024a0003c0003t0021a0003c0003t0032 | 3 | HG02717.hp2 HG02922.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1102C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1102 | chr10 | 113167074 | |||||
| chr10:113167151
|
A | G | 1 | a0001c0001t0023 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1179A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1179 | chr10 | 113167151 | |||||
| chr10:113167361
|
C | A | 2 | a0001c0001t0040a0001c0001t0043 | 2 | HG00323.hp2 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1389C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1389 | chr10 | 113167361 | |||||
| chr10:113167456
|
C | T | 1 | a0001c0001t0037 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1484C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 15/15 | 1484 | chr10 | 113167456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:112951110
|
AC | A | 34 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0002g0161others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.190-89delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 112951110 | |||||
| chr10:112951117
|
C | T | 12 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0193others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-90C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 1/14 | chr10 | 112951117 | ||||||
| chr10:112951394
|
G | A | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.257-89G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 2/14 | chr10 | 112951394 | ||||||
| chr10:112951635
|
C | A | 12 | a0001c0001t0002g0006a0001c0001t0002g0012a0001c0001t0006g0005others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+28C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112951635 | ||||||
| chr10:112951656
|
C | A | 1 | a0007c0008t0002g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.381+49C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112951656 | ||||||
| chr10:112951744
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.381+137G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112951744 | ||||||
| chr10:112951893
|
A | AG | 29 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0003g0163others(26): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.381+294dupG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112951893 | |||||
| chr10:112951913
|
C | CT | 120 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.381+309dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112951913 | |||||
| chr10:112951918
|
C | T | 120 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.381+311C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112951918 | ||||||
| chr10:112951996
|
C | T | 120 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.381+389C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112951996 | ||||||
| chr10:112952009
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | NA19063.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.381+402T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952009 | ||||||
| chr10:112952081
|
C | T | 1 | a0002c0002t0001g0090 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.381+474C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952081 | ||||||
| chr10:112952124
|
G | A | 14 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0003g0163others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.381+517G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952124 | ||||||
| chr10:112952182
|
C | T | 1 | a0001c0001t0014g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+575C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952182 | ||||||
| chr10:112952224
|
A | G | 120 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.381+617A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952224 | ||||||
| chr10:112952262
|
C | T | 2 | a0001c0001t0006g0188a0001c0001t0034g0187 | 2 | HG01243.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.381+655C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952262 | ||||||
| chr10:112952395
|
C | G | 120 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.381+788C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952395 | ||||||
| chr10:112952491
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.381+884G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952491 | ||||||
| chr10:112952537
|
G | A | 1 | a0001c0001t0015g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.381+930G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952537 | ||||||
| chr10:112952548
|
C | T | 3 | a0001c0001t0013g0151a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02145.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.381+941C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952548 | ||||||
| chr10:112952560
|
T | C | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.381+953T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952560 | ||||||
| chr10:112952752
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.381+1145C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952752 | ||||||
| chr10:112952789
|
A | T | 24 | a0001c0001t0002g0161a0001c0001t0002g0173a0001c0001t0003g0163others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.381+1182A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952789 | ||||||
| chr10:112952835
|
G | C | 96 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(93): Show | 96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.381+1228G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952835 | ||||||
| chr10:112952838
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0089a0002c0002t0001g0088 | 3 | HG00438.hp2 HG00597.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.381+1231C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952838 | ||||||
| chr10:112952976
|
G | T | 1 | a0001c0001t0003g0174 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.381+1369G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112952976 | ||||||
| chr10:112953216
|
A | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+1609A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112953216 | ||||||
| chr10:112953251
|
C | A | 1 | a0001c0001t0034g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.381+1644C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112953251 | ||||||
| chr10:112953297
|
G | A | 1 | a0001c0001t0034g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.381+1690G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112953297 | ||||||
| chr10:112953675
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.381+2068G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112953675 | ||||||
| chr10:112953708
|
G | A | 1 | a0001c0001t0007g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.381+2101G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112953708 | ||||||
| chr10:112954191
|
GT | G | 94 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.381+2589delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112954191 | |||||
| chr10:112954250
|
C | T | 1 | a0001c0001t0034g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.381+2643C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112954250 | ||||||
| chr10:112954379
|
TAGAG | T | 2 | a0001c0001t0006g0188a0001c0001t0034g0187 | 2 | HG01243.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.381+2775_381+2778d others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112954379 | |||||
| chr10:112954728
|
G | T | 5 | a0001c0001t0001g0086a0001c0001t0002g0173a0001c0001t0003g0172others(2): Show | 5 | HG01978.hp2 HG01981.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+3121G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112954728 | ||||||
| chr10:112954729
|
T | G | 96 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(93): Show | 96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.381+3122T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112954729 | ||||||
| chr10:112954938
|
C | G | 1 | a0001c0001t0034g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.381+3331C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112954938 | ||||||
| chr10:112954962
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.381+3355C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112954962 | ||||||
| chr10:112954966
|
C | T | 94 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.381+3359C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112954966 | ||||||
| chr10:112955101
|
C | T | 4 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0145others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+3494C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955101 | ||||||
| chr10:112955102
|
C | A | 4 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0145others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+3495C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955102 | ||||||
| chr10:112955111
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.381+3504C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955111 | ||||||
| chr10:112955158
|
C | A | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(10): Show | 13 | HG02132.hp1 HG02165.hp1 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+3551C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955158 | ||||||
| chr10:112955241
|
A | G | 7 | a0001c0001t0002g0094a0001c0001t0002g0142a0001c0001t0006g0149others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+3634A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955241 | ||||||
| chr10:112955421
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.381+3814A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955421 | ||||||
| chr10:112955641
|
C | T | 1 | a0001c0001t0007g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+4034C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955641 | ||||||
| chr10:112955707
|
A | T | 2 | a0001c0001t0014g0083a0003c0003t0004g0084 | 2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.381+4100A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955707 | ||||||
| chr10:112955772
|
A | G | 96 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(93): Show | 96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.381+4165A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955772 | ||||||
| chr10:112955839
|
G | A | 115 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.381+4232G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955839 | ||||||
| chr10:112955930
|
C | T | 94 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.381+4323C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955930 | ||||||
| chr10:112955985
|
G | C | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+4378G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112955985 | ||||||
| chr10:112956171
|
A | G | 20 | a0001c0001t0002g0161a0001c0001t0003g0163a0001c0001t0003g0170others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.381+4564A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112956171 | ||||||
| chr10:112956344
|
CT | C | 85 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.381+4760delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112956344 | |||||
| chr10:112956344
|
CTT | C | 9 | a0001c0001t0001g0031a0001c0001t0002g0161a0001c0001t0007g0020others(6): Show | 9 | HG00280.hp2 HG02165.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+4759_381+4760d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112956344 | |||||
| chr10:112956367
|
T | A | 11 | a0001c0001t0001g0190a0001c0001t0002g0096a0001c0001t0002g0142others(8): Show | 11 | HG01081.hp1 HG01255.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.381+4760T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112956367 | ||||||
| chr10:112956367
|
T | TA | 73 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(70): Show | 73 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.381+4763dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112956367 | |||||
| chr10:112956367
|
T | TTA | 8 | a0001c0001t0002g0094a0001c0001t0004g0141a0001c0001t0006g0140others(5): Show | 8 | HG00597.hp1 HG01109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+4760_381+4761i others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112956367 | ||||||
| chr10:112956997
|
G | T | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.381+5390G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112956997 | ||||||
| chr10:112957142
|
C | T | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098 | 3 | HG03130.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.381+5535C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112957142 | ||||||
| chr10:112957190
|
C | CT | 32 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.381+5609dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112957190 | |||||
| chr10:112957190
|
CT | C | 27 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(24): Show | 27 | HG01070.hp2 HG01099.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+5609delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112957190 | |||||
| chr10:112957190
|
CTT | C | 70 | a0001c0001t0001g0101a0001c0001t0001g0123a0001c0001t0001g0125others(67): Show | 70 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.381+5608_381+5609d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112957190 | |||||
| chr10:112957190
|
CTTT | C | 16 | a0001c0001t0001g0099a0001c0001t0002g0006a0001c0001t0002g0012others(13): Show | 16 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.381+5607_381+5609d others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112957190 | |||||
| chr10:112957190
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.381+5599_381+5609d others(13): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112957190 | |||||
| chr10:112957355
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.381+5748T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112957355 | ||||||
| chr10:112957430
|
A | G | 94 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.381+5823A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112957430 | ||||||
| chr10:112957431
|
A | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+5824A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112957431 | ||||||
| chr10:112957535
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.381+5928T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112957535 | ||||||
| chr10:112957659
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG01943.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.381+6052T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112957659 | ||||||
| chr10:112957712
|
C | G | 88 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(85): Show | 88 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.381+6105C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112957712 | ||||||
| chr10:112958122
|
C | G | 1 | a0001c0001t0042g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.382-6434C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112958122 | ||||||
| chr10:112958909
|
G | T | 3 | a0001c0001t0013g0151a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02145.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.382-5647G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112958909 | ||||||
| chr10:112959099
|
A | G | 5 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098others(2): Show | 5 | HG02559.hp1 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5457A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112959099 | ||||||
| chr10:112959133
|
C | T | 6 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0006g0157others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-5423C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112959133 | ||||||
| chr10:112959170
|
C | CT | 94 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0129others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.382-5375dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112959170 | |||||
| chr10:112959613
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.382-4943G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112959613 | ||||||
| chr10:112959622
|
A | T | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.382-4934A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112959622 | ||||||
| chr10:112959735
|
C | T | 1 | a0001c0001t0034g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.382-4821C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112959735 | ||||||
| chr10:112959982
|
GT | G | 112 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(109): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.382-4563delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112959982 | |||||
| chr10:112960150
|
T | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382-4406T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112960150 | ||||||
| chr10:112960181
|
G | A | 2 | a0001c0001t0006g0188a0001c0001t0034g0187 | 2 | HG01243.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.382-4375G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112960181 | ||||||
| chr10:112960235
|
A | G | 85 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(82): Show | 85 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.382-4321A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112960235 | ||||||
| chr10:112960691
|
G | GT | 98 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.382-3852dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112960691 | |||||
| chr10:112960717
|
C | T | 2 | a0001c0001t0011g0176a0001c0001t0042g0177 | 2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-3839C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112960717 | ||||||
| chr10:112961044
|
T | A | 3 | a0001c0001t0013g0151a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02145.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.382-3512T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961044 | ||||||
| chr10:112961117
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.382-3439G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961117 | ||||||
| chr10:112961123
|
C | T | 33 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.382-3433C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961123 | ||||||
| chr10:112961170
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-3386C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961170 | ||||||
| chr10:112961227
|
C | G | 1 | a0001c0001t0004g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.382-3329C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961227 | ||||||
| chr10:112961254
|
A | AC | 25 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0040others(22): Show | 25 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.382-3289dupC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACC | 12 | a0001c0001t0001g0061a0001c0001t0001g0074a0001c0001t0001g0086others(9): Show | 12 | HG01978.hp2 HG01981.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-3290_382-3289d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCC | 19 | a0001c0001t0002g0006a0001c0001t0002g0100a0001c0001t0002g0107others(16): Show | 19 | HG00741.hp1 HG01346.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.382-3300_382-3299i others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC | 15 | a0001c0001t0001g0193a0001c0001t0002g0096a0001c0001t0002g0113others(12): Show | 15 | HG00741.hp2 HG01175.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.382-3300_382-3299i others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(1): Show |
12 | a0001c0001t0001g0131a0001c0001t0001g0190a0001c0001t0001g0194others(9): Show | 12 | HG00642.hp1 HG01515.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.382-3300_382-3299i others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(3): Show |
10 | a0001c0001t0001g0195a0001c0001t0002g0012a0001c0001t0005g0033others(7): Show | 10 | HG00438.hp1 HG01081.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-3300_382-3299i others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(4): Show |
9 | a0001c0001t0001g0123a0001c0001t0001g0196a0001c0001t0001g0197others(6): Show | 9 | HG01123.hp1 HG02280.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-3300_382-3299i others(13): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(5): Show |
3 | a0001c0005t0006g0138a0001c0005t0019g0001a0001c0005t0019g0002 | 3 | HG02896.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.382-3300_382-3299i others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(6): Show |
6 | a0001c0001t0001g0101a0001c0001t0001g0125a0001c0001t0004g0126others(3): Show | 6 | HG02040.hp1 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-3300_382-3299i others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(8): Show |
2 | a0001c0001t0004g0132a0001c0001t0010g0127 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.382-3300_382-3299i others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(9): Show |
1 | a0001c0001t0001g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382-3300_382-3299i others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
A | ACCGCCCC others(11): Show |
2 | a0001c0001t0004g0133a0007c0008t0002g0015 | 2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.382-3300_382-3299i others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961254
|
AC | A | 21 | a0001c0001t0001g0041a0001c0001t0002g0102a0001c0001t0002g0161others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-3289delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961254 | |||||
| chr10:112961256
|
C | CA | 2 | a0001c0001t0001g0079a0001c0001t0004g0076 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.382-3300_382-3299i others(3): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961256 | ||||||
| chr10:112961259
|
C | G | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382-3297C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961259 | ||||||
| chr10:112961261
|
C | G | 8 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0139others(5): Show | 8 | HG02559.hp1 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-3295C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961261 | ||||||
| chr10:112961263
|
C | A | 1 | a0001c0001t0012g0169 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.382-3293C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961263 | ||||||
| chr10:112961263
|
C | G | 2 | a0001c0001t0001g0058a0001c0001t0009g0057 | 2 | HG01358.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.382-3293C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961263 | ||||||
| chr10:112961264
|
C | A | 20 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0163others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.382-3292C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961264 | ||||||
| chr10:112961266
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382-3290C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961266 | ||||||
| chr10:112961267
|
C | G | 20 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0163others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.382-3289C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961267 | ||||||
| chr10:112961346
|
G | A | 95 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(92): Show | 95 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.382-3210G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961346 | ||||||
| chr10:112961475
|
A | G | 7 | a0001c0001t0002g0094a0001c0001t0006g0136a0001c0001t0006g0137others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-3081A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961475 | ||||||
| chr10:112961478
|
A | G | 127 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.382-3078A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961478 | ||||||
| chr10:112961645
|
A | G | 154 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0046others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.382-2911A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961645 | ||||||
| chr10:112961704
|
G | A | 21 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG01256.hp1 HG01258.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.382-2852G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961704 | ||||||
| chr10:112961809
|
G | C | 117 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0046others(114): Show | 117 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.382-2747G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961809 | ||||||
| chr10:112961847
|
C | T | 1 | a0002c0002t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382-2709C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961847 | ||||||
| chr10:112961876
|
C | T | 2 | a0001c0001t0004g0075a0001c0001t0029g0114 | 2 | HG02647.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.382-2680C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961876 | ||||||
| chr10:112961893
|
A | ATG | 37 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(34): Show | 37 | HG00140.hp1 HG01081.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.382-2646_382-2645d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961893 | |||||
| chr10:112961893
|
ATG | A | 3 | a0001c0001t0016g0023a0001c0001t0023g0027a0001c0001t0034g0187 | 3 | HG01496.hp2 HG02165.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.382-2646_382-2645d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961893 | |||||
| chr10:112961908
|
TGTGA | T | 4 | a0001c0001t0002g0094a0001c0001t0006g0136a0001c0001t0006g0137others(1): Show | 4 | HG03130.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2646_382-2643d others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961908 | |||||
| chr10:112961910
|
T | A | 3 | a0001c0001t0013g0151a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02145.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.382-2646T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961910 | ||||||
| chr10:112961910
|
TGA | T | 7 | a0001c0001t0004g0016a0001c0001t0004g0097a0001c0001t0008g0092others(4): Show | 7 | HG01884.hp2 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-2631_382-2630d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112961910 | |||||
| chr10:112961912
|
A | T | 93 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(90): Show | 93 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.382-2644A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961912 | ||||||
| chr10:112961914
|
A | T | 8 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0139others(5): Show | 8 | HG01109.hp2 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-2642A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112961914 | ||||||
| chr10:112962015
|
A | G | 13 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(10): Show | 13 | HG00140.hp1 HG01256.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.382-2541A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962015 | ||||||
| chr10:112962115
|
G | T | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.382-2441G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962115 | ||||||
| chr10:112962123
|
T | C | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.382-2433T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962123 | ||||||
| chr10:112962204
|
A | G | 1 | a0001c0004t0013g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.382-2352A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962204 | ||||||
| chr10:112962235
|
G | C | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.382-2321G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962235 | ||||||
| chr10:112962367
|
C | G | 3 | a0001c0001t0013g0151a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02145.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.382-2189C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962367 | ||||||
| chr10:112962375
|
CT | C | 141 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(138): Show | 141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.382-2178delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112962375 | |||||
| chr10:112962475
|
T | A | 8 | a0001c0001t0002g0158a0001c0001t0006g0136a0001c0001t0006g0137others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-2081T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962475 | ||||||
| chr10:112962521
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.382-2035C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962521 | ||||||
| chr10:112962656
|
C | T | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.382-1900C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962656 | ||||||
| chr10:112962694
|
G | A | 12 | a0001c0001t0002g0006a0001c0001t0002g0012a0001c0001t0002g0095others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-1862G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962694 | ||||||
| chr10:112962791
|
G | A | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382-1765G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962791 | ||||||
| chr10:112962853
|
C | T | 8 | a0001c0001t0002g0158a0001c0001t0006g0136a0001c0001t0006g0137others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-1703C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962853 | ||||||
| chr10:112962857
|
C | A | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.382-1699C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962857 | ||||||
| chr10:112962862
|
G | A | 120 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 120 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.382-1694G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962862 | ||||||
| chr10:112962901
|
C | T | 8 | a0001c0001t0002g0158a0001c0001t0006g0136a0001c0001t0006g0137others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-1655C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112962901 | ||||||
| chr10:112963154
|
T | A | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.382-1402T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963154 | ||||||
| chr10:112963176
|
A | G | 12 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-1380A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963176 | ||||||
| chr10:112963195
|
G | C | 105 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(102): Show | 105 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.382-1361G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963195 | ||||||
| chr10:112963221
|
AT | A | 6 | a0001c0001t0006g0149a0001c0001t0006g0188a0001c0001t0010g0127others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-1327delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112963221 | |||||
| chr10:112963543
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.382-1013C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963543 | ||||||
| chr10:112963624
|
A | G | 1 | a0001c0001t0005g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.382-932A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963624 | ||||||
| chr10:112963759
|
T | C | 1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.382-797T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963759 | ||||||
| chr10:112963800
|
T | C | 120 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(117): Show | 120 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.382-756T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963800 | ||||||
| chr10:112963891
|
C | T | 44 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.382-665C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112963891 | ||||||
| chr10:112963936
|
T | TA | 2 | a0001c0001t0016g0023a0001c0001t0016g0024 | 2 | HG02165.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.382-619dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112963936 | |||||
| chr10:112964086
|
A | C | 1 | a0001c0001t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.382-470A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112964086 | ||||||
| chr10:112964098
|
A | G | 122 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(119): Show | 122 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.382-458A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112964098 | ||||||
| chr10:112964227
|
C | T | 3 | a0001c0001t0014g0083a0003c0003t0004g0084a0004c0006t0001g0053 | 3 | HG01109.hp1 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.382-329C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112964227 | ||||||
| chr10:112964341
|
AAAAAACA others(5): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-197_382-186del others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr10 | 112964341 | |||||
| chr10:112964408
|
G | A | 1 | a0001c0013t0027g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.382-148G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 3/14 | chr10 | 112964408 | ||||||
| chr10:112964633
|
C | T | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.450+9C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964633 | ||||||
| chr10:112964711
|
GATA | G | 8 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+90_450+92delAA others(1): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964711 | |||||
| chr10:112964714
|
A | G | 112 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.450+90A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964714 | ||||||
| chr10:112964739
|
A | ATGATGG | 2 | a0001c0001t0016g0023a0001c0001t0016g0024 | 2 | HG02165.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.450+117_450+118ins others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964739 | |||||
| chr10:112964739
|
A | ATGATGGT others(2): Show |
9 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0139others(6): Show | 9 | HG01109.hp2 HG02723.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.450+117_450+118ins others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964739 | |||||
| chr10:112964739
|
A | G | 12 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0002g0094others(9): Show | 12 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.450+115A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964739 | ||||||
| chr10:112964739
|
ATGGTGG | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0195 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.450+130_450+135del others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964739 | |||||
| chr10:112964742
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0004g0126others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+118G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964742 | ||||||
| chr10:112964742
|
G | GTGGTGGT others(11): Show |
8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0058others(5): Show | 8 | HG00140.hp1 HG00741.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+151_450+168dup others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964742 | |||||
| chr10:112964742
|
G | GTGGTGGT others(29): Show |
1 | a0001c0001t0001g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.450+133_450+168dup others(36): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964742 | |||||
| chr10:112964745
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0004g0126others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+121G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964745 | ||||||
| chr10:112964745
|
G | GTGGTGGT others(26): Show |
9 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0190others(6): Show | 9 | HG00597.hp1 HG00735.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.450+154_450+186dup others(33): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964745 | |||||
| chr10:112964745
|
G | GTGGTGGT others(29): Show |
1 | a0002c0002t0018g0022 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.450+135_450+136ins others(36): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964745 | |||||
| chr10:112964760
|
ATGG | A | 17 | a0001c0001t0001g0129a0001c0001t0002g0006a0001c0001t0002g0012others(14): Show | 17 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.450+151_450+153del others(3): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964760 | |||||
| chr10:112964769
|
GTGGTGGT others(2): Show |
G | 4 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0148others(1): Show | 4 | HG03130.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+154_450+162del others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964769 | |||||
| chr10:112964775
|
G | A | 1 | a0001c0001t0013g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.450+151G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964775 | ||||||
| chr10:112964778
|
A | ATGGTGGT others(11): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0012g0154 | 3 | HG00642.hp2 HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.450+169_450+186dup others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964778 | |||||
| chr10:112964778
|
A | G | 6 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0004g0126others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+154A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964778 | ||||||
| chr10:112964784
|
G | A | 5 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0004g0126others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+160G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964784 | ||||||
| chr10:112964790
|
G | A | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.450+166G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964790 | ||||||
| chr10:112964793
|
A | G | 5 | a0001c0001t0001g0059a0001c0001t0001g0125a0001c0001t0004g0126others(2): Show | 5 | HG00408.hp1 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+169A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964793 | ||||||
| chr10:112964793
|
ATGG | A | 2 | a0001c0001t0011g0176a0003c0003t0011g0009 | 2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.450+188_450+190del others(3): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964793 | |||||
| chr10:112964796
|
G | GTGGTGGT others(23): Show |
11 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0078others(8): Show | 11 | HG01070.hp2 HG01358.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+186_450+187ins others(30): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964796 | |||||
| chr10:112964801
|
GGTGGTGG others(4): Show |
G | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.450+179_450+189del others(11): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964801 | |||||
| chr10:112964807
|
GGT | G | 3 | a0001c0001t0002g0006a0001c0001t0002g0012a0001c0001t0030g0004 | 3 | HG01884.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.450+185_450+186del others(2): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964807 | |||||
| chr10:112964808
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0005g0122a0001c0001t0011g0175others(1): Show | 4 | HG01081.hp1 HG01123.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+184G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964808 | ||||||
| chr10:112964808
|
GTGGT | G | 2 | a0001c0001t0033g0003a0001c0001t0042g0177 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.450+185_450+188del others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964808 | ||||||
| chr10:112964809
|
T | TGATGGTG others(27): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(4): Show | 7 | HG00408.hp2 HG01099.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+186_450+187ins others(34): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964809 | |||||
| chr10:112964809
|
T | TGATGGTG others(28): Show |
4 | a0001c0001t0007g0189a0001c0001t0023g0027a0002c0002t0001g0028others(1): Show | 4 | HG02040.hp1 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+186_450+187ins others(35): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964809 | |||||
| chr10:112964810
|
G | T | 5 | a0001c0001t0008g0139a0001c0001t0010g0127a0001c0001t0013g0151others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+186G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964810 | ||||||
| chr10:112964810
|
GGT | G | 14 | a0001c0001t0001g0129a0001c0001t0002g0095a0001c0001t0002g0173others(11): Show | 14 | HG01978.hp2 HG01981.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.450+188_450+189del others(2): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964810 | |||||
| chr10:112964811
|
G | A | 11 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(8): Show | 11 | HG00280.hp2 HG00738.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+187G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964811 | ||||||
| chr10:112964811
|
GT | G | 10 | a0001c0001t0001g0131a0001c0001t0004g0134a0001c0001t0008g0139others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.450+188delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964811 | ||||||
| chr10:112964812
|
T | G | 39 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(36): Show | 39 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.450+188T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964812 | ||||||
| chr10:112964812
|
T | TGGTGGTG others(43): Show |
1 | a0001c0001t0005g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.450+190_450+191ins others(50): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964812 | |||||
| chr10:112964812
|
TG | T | 17 | a0001c0001t0002g0158a0001c0001t0006g0136a0001c0001t0006g0137others(14): Show | 17 | HG01109.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.450+197delG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964812 | |||||
| chr10:112964813
|
G | GATGGTGG others(22): Show |
4 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+189_450+190ins others(29): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964813 | ||||||
| chr10:112964813
|
G | GGTGATGG others(55): Show |
1 | a0001c0001t0001g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.450+190_450+191ins others(62): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964813 | |||||
| chr10:112964813
|
G | GGTGGTGG others(37): Show |
2 | a0001c0001t0011g0175a0001c0001t0011g0184 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.450+190_450+191ins others(44): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964813 | |||||
| chr10:112964813
|
G | GGTGGTGG others(22): Show |
1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.450+190_450+191ins others(29): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964813 | |||||
| chr10:112964813
|
G | GGTGGTGG others(25): Show |
11 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(8): Show | 11 | HG00280.hp2 HG00738.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+190_450+191ins others(32): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112964813 | |||||
| chr10:112964815
|
G | T | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.450+191G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964815 | ||||||
| chr10:112964819
|
G | C | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0002g0155others(5): Show | 8 | HG00140.hp1 HG00741.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+195G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964819 | ||||||
| chr10:112964820
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.450+196G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964820 | ||||||
| chr10:112964837
|
A | C | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+213A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964837 | ||||||
| chr10:112964904
|
A | C | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+280A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964904 | ||||||
| chr10:112964911
|
G | C | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+287G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112964911 | ||||||
| chr10:112965047
|
T | C | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+423T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965047 | ||||||
| chr10:112965049
|
A | T | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+425A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965049 | ||||||
| chr10:112965051
|
G | A | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+427G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965051 | ||||||
| chr10:112965185
|
A | G | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.450+561A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965185 | ||||||
| chr10:112965320
|
G | A | 12 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(9): Show | 12 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.450+696G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965320 | ||||||
| chr10:112965329
|
C | G | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.450+705C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965329 | ||||||
| chr10:112965490
|
G | A | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+866G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965490 | ||||||
| chr10:112965505
|
G | T | 5 | a0001c0001t0008g0139a0001c0001t0010g0127a0001c0001t0013g0151others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+881G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965505 | ||||||
| chr10:112965607
|
T | A | 2 | a0001c0001t0001g0074a0001c0005t0006g0138 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.450+983T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965607 | ||||||
| chr10:112965615
|
CTGTGTGT others(7): Show |
C | 2 | a0001c0001t0007g0085a0009c0007t0001g0025 | 2 | HG00735.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.450+1003_450+1016d others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965615 | |||||
| chr10:112965615
|
CTGTGTGT others(9): Show |
C | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.450+1003_450+1018d others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965615 | |||||
| chr10:112965615
|
CTGTGTGT others(11): Show |
C | 2 | a0001c0001t0001g0191a0001c0001t0001g0195 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.450+1003_450+1020d others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965615 | |||||
| chr10:112965619
|
GTGTGTGT others(3): Show |
G | 16 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 16 | HG00140.hp1 HG00741.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.450+1003_450+1012d others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965619 | |||||
| chr10:112965629
|
A | ATG | 3 | a0001c0001t0006g0140a0001c0001t0011g0175a0001c0001t0016g0024 | 3 | HG01081.hp1 NA18964.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.450+1052_450+1053d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0004g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.450+1044_450+1053d others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
ATG | A | 17 | a0001c0001t0001g0074a0001c0001t0001g0082a0001c0001t0002g0006others(14): Show | 17 | HG01071.hp1 HG01099.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.450+1052_450+1053d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
ATGTG | A | 23 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0056others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.450+1050_450+1053d others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
ATGTGTG | A | 54 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0041others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.450+1048_450+1053d others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
ATGTGTGT others(1): Show |
A | 11 | a0001c0001t0002g0104a0001c0001t0002g0117a0001c0001t0002g0128others(8): Show | 11 | HG00323.hp1 HG01433.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+1046_450+1053d others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
ATGTGTGT others(3): Show |
A | 28 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0001g0099others(25): Show | 28 | HG00323.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.450+1044_450+1053d others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0002g0107a0001c0001t0002g0108 | 2 | HG01346.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.450+1042_450+1053d others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965629
|
ATGTGTGT others(7): Show |
A | 5 | a0001c0001t0008g0139a0001c0001t0010g0127a0001c0001t0013g0151others(2): Show | 5 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+1040_450+1053d others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112965629 | |||||
| chr10:112965637
|
G | A | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.450+1013G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965637 | ||||||
| chr10:112965639
|
G | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 16 | HG00140.hp1 HG00741.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.450+1015G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965639 | ||||||
| chr10:112965643
|
G | A | 2 | a0001c0001t0007g0085a0009c0007t0001g0025 | 2 | HG00735.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.450+1019G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965643 | ||||||
| chr10:112965645
|
G | A | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.450+1021G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965645 | ||||||
| chr10:112965647
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0195 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.450+1023G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965647 | ||||||
| chr10:112965850
|
A | C | 24 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0123others(21): Show | 24 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.450+1226A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965850 | ||||||
| chr10:112965898
|
G | T | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.450+1274G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965898 | ||||||
| chr10:112965994
|
T | C | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.450+1370T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112965994 | ||||||
| chr10:112966060
|
A | T | 2 | a0001c0001t0001g0074a0001c0005t0006g0138 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.450+1436A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966060 | ||||||
| chr10:112966078
|
G | A | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098 | 3 | HG03130.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.450+1454G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966078 | ||||||
| chr10:112966115
|
C | T | 3 | a0001c0001t0002g0104a0001c0001t0002g0117a0001c0001t0036g0116 | 3 | HG00323.hp1 HG01515.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.450+1491C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966115 | ||||||
| chr10:112966167
|
C | T | 109 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.450+1543C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966167 | ||||||
| chr10:112966177
|
A | AATATACA others(19): Show |
1 | a0001c0001t0001g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.450+1558_450+1559i others(28): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966177 | |||||
| chr10:112966177
|
A | AATATATA others(21): Show |
1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.450+1559_450+1560i others(30): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966177 | |||||
| chr10:112966177
|
A | AATATATA others(23): Show |
1 | a0001c0001t0004g0126 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.450+1559_450+1560i others(32): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966177 | |||||
| chr10:112966177
|
A | AATATATA others(29): Show |
2 | a0001c0001t0001g0125a0001c0001t0026g0124 | 2 | HG02145.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450+1559_450+1560i others(38): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966177 | |||||
| chr10:112966184
|
T | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0123a0001c0001t0001g0125others(3): Show | 6 | HG00438.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+1560T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966184 | ||||||
| chr10:112966184
|
T | TTATATA | 6 | a0001c0001t0001g0129a0001c0001t0002g0158a0001c0001t0011g0159others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+1582_450+1587d others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(5): Show |
3 | a0001c0001t0006g0137a0001c0001t0028g0014a0002c0002t0007g0198 | 3 | HG02040.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.450+1576_450+1587d others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0101a0001c0001t0006g0136a0001c0001t0010g0098 | 3 | HG03130.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.450+1574_450+1587d others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(11): Show |
3 | a0001c0001t0002g0142a0001c0001t0006g0149a0001c0001t0031g0010 | 3 | HG03041.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.450+1570_450+1587d others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+1568_450+1587d others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(15): Show |
1 | a0001c0001t0002g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.450+1566_450+1587d others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(17): Show |
3 | a0001c0001t0001g0099a0001c0001t0006g0007a0003c0003t0011g0009 | 3 | HG02572.hp2 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.450+1564_450+1587d others(26): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0033g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.450+1562_450+1587d others(28): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(23): Show |
3 | a0001c0001t0002g0006a0001c0001t0045g0156a0001c0004t0008g0146 | 3 | HG02109.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.450+1587_450+1588i others(32): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(25): Show |
3 | a0001c0001t0006g0140a0001c0001t0008g0092a0001c0001t0008g0093 | 3 | HG02895.hp1 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.450+1587_450+1588i others(34): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(27): Show |
3 | a0001c0001t0002g0095a0001c0001t0042g0177a0001c0004t0013g0147 | 3 | HG01109.hp2 HG02258.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.450+1587_450+1588i others(36): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(29): Show |
7 | a0001c0001t0006g0005a0001c0001t0006g0013a0001c0001t0013g0103others(4): Show | 7 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+1587_450+1588i others(38): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(31): Show |
2 | a0001c0001t0002g0094a0001c0001t0004g0132 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.450+1587_450+1588i others(40): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(33): Show |
1 | a0001c0001t0013g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450+1587_450+1588i others(42): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(37): Show |
1 | a0001c0001t0029g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.450+1587_450+1588i others(46): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(7): Show |
17 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(14): Show | 17 | HG00408.hp2 HG00735.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.450+1569_450+1570i others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(9): Show |
15 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.450+1569_450+1570i others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(11): Show |
5 | a0001c0001t0001g0194a0001c0001t0002g0155a0001c0001t0023g0027others(2): Show | 5 | HG02683.hp1 HG02735.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+1569_450+1570i others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(15): Show |
2 | a0001c0001t0001g0017a0001c0001t0005g0033 | 2 | HG03942.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.450+1569_450+1570i others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(17): Show |
2 | a0001c0001t0004g0075a0001c0001t0022g0050 | 2 | HG01358.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.450+1569_450+1570i others(26): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0001g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.450+1569_450+1570i others(28): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.450+1569_450+1570i others(36): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATTT others(9): Show |
1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.450+1565_450+1566i others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
T | TTATATTT others(35): Show |
1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.450+1565_450+1566i others(44): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
TTA | T | 56 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0038others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.450+1586_450+1587d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966184
|
TTATA | T | 34 | a0001c0001t0001g0051a0001c0001t0001g0062a0001c0001t0001g0063others(31): Show | 34 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.450+1584_450+1587d others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966184 | |||||
| chr10:112966186
|
A | T | 2 | a0001c0001t0011g0175a0001c0001t0011g0184 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.450+1562A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966186 | ||||||
| chr10:112966190
|
A | T | 8 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+1566A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966190 | ||||||
| chr10:112966208
|
A | ATATATAT others(23): Show |
1 | a0001c0004t0013g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.450+1587_450+1588i others(32): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966208 | |||||
| chr10:112966209
|
T | TATATATA others(6): Show |
1 | a0001c0001t0002g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.450+1587_450+1588i others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(20): Show |
1 | a0001c0001t0011g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.450+1587_450+1588i others(29): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(24): Show |
1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.450+1587_450+1588i others(33): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(26): Show |
1 | a0001c0001t0005g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.450+1587_450+1588i others(35): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(28): Show |
1 | a0001c0001t0011g0184 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.450+1587_450+1588i others(37): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(30): Show |
1 | a0005c0010t0003g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.450+1587_450+1588i others(39): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(34): Show |
2 | a0001c0001t0003g0179a0001c0001t0012g0178 | 2 | HG00280.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.450+1587_450+1588i others(43): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(36): Show |
1 | a0001c0001t0041g0180 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.450+1587_450+1588i others(45): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966209
|
T | TATATATA others(40): Show |
1 | a0001c0001t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.450+1587_450+1588i others(49): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112966209 | |||||
| chr10:112966244
|
G | T | 10 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.450+1620G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966244 | ||||||
| chr10:112966294
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.450+1670A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966294 | ||||||
| chr10:112966418
|
T | A | 109 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.450+1794T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966418 | ||||||
| chr10:112966429
|
A | T | 1 | a0002c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.450+1805A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966429 | ||||||
| chr10:112966443
|
C | T | 3 | a0001c0001t0003g0179a0001c0001t0004g0126a0001c0001t0012g0178 | 3 | HG00280.hp2 HG01256.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.450+1819C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966443 | ||||||
| chr10:112966458
|
G | A | 2 | a0001c0001t0001g0074a0001c0005t0006g0138 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.450+1834G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966458 | ||||||
| chr10:112966770
|
T | C | 8 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0013g0103others(5): Show | 8 | HG01109.hp2 HG02280.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2146T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966770 | ||||||
| chr10:112966830
|
C | G | 5 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0008g0148others(2): Show | 5 | HG02809.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+2206C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112966830 | ||||||
| chr10:112967049
|
G | GC | 121 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(118): Show | 121 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.450+2425_450+2426i others(3): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967049 | ||||||
| chr10:112967084
|
G | A | 44 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.450+2460G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967084 | ||||||
| chr10:112967145
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450+2521C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967145 | ||||||
| chr10:112967190
|
C | G | 1 | a0001c0001t0029g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.450+2566C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967190 | ||||||
| chr10:112967308
|
C | T | 44 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(41): Show | 44 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.450+2684C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967308 | ||||||
| chr10:112967460
|
T | C | 2 | a0002c0002t0001g0021a0002c0002t0001g0028 | 2 | HG02683.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.450+2836T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967460 | ||||||
| chr10:112967540
|
C | CT | 2 | a0001c0001t0002g0094a0001c0001t0004g0132 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.450+2917dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112967540 | |||||
| chr10:112967605
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.450+2981A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967605 | ||||||
| chr10:112967629
|
T | C | 1 | a0001c0001t0017g0052 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.450+3005T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967629 | ||||||
| chr10:112967635
|
G | GT | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.450+3027dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112967635 | |||||
| chr10:112967635
|
G | GTT | 5 | a0001c0001t0005g0199a0001c0001t0007g0189a0001c0001t0015g0008others(2): Show | 5 | HG01109.hp2 HG02738.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+3026_450+3027d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112967635 | |||||
| chr10:112967657
|
G | T | 5 | a0001c0001t0001g0129a0001c0001t0002g0158a0001c0001t0004g0076others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+3033G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967657 | ||||||
| chr10:112967721
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+3097C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967721 | ||||||
| chr10:112967815
|
A | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+3191A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112967815 | ||||||
| chr10:112968179
|
C | T | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+3555C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112968179 | ||||||
| chr10:112968328
|
A | G | 1 | a0002c0002t0018g0022 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.450+3704A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112968328 | ||||||
| chr10:112968381
|
C | A | 8 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+3757C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112968381 | ||||||
| chr10:112968955
|
C | T | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.450+4331C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112968955 | ||||||
| chr10:112969382
|
CT | C | 3 | a0001c0001t0013g0151a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02145.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.450+4759delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969382 | ||||||
| chr10:112969385
|
C | A | 3 | a0001c0001t0013g0151a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02145.hp1 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.450+4761C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969385 | ||||||
| chr10:112969465
|
G | T | 3 | a0001c0001t0002g0095a0001c0005t0019g0001a0001c0005t0019g0002 | 3 | HG02258.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.450+4841G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969465 | ||||||
| chr10:112969632
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.450+5008C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969632 | ||||||
| chr10:112969723
|
T | G | 22 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0002g0100others(19): Show | 22 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.450+5099T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969723 | ||||||
| chr10:112969744
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0014g0055 | 2 | HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.450+5120T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969744 | ||||||
| chr10:112969804
|
C | A | 109 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.450+5180C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969804 | ||||||
| chr10:112969937
|
A | G | 10 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.450+5313A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112969937 | ||||||
| chr10:112970166
|
T | TTG | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.450+5561_450+5562d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112970166 | |||||
| chr10:112970185
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.450+5561T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970185 | ||||||
| chr10:112970188
|
A | G | 8 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+5564A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970188 | ||||||
| chr10:112970344
|
C | T | 3 | a0001c0001t0002g0094a0001c0001t0002g0142a0001c0001t0004g0132 | 3 | HG02622.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.450+5720C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970344 | ||||||
| chr10:112970444
|
A | G | 2 | a0001c0001t0016g0023a0001c0001t0016g0024 | 2 | HG02165.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.450+5820A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970444 | ||||||
| chr10:112970634
|
C | T | 2 | a0001c0001t0045g0156a0006c0012t0007g0026 | 2 | HG02109.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.450+6010C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970634 | ||||||
| chr10:112970737
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+6113C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970737 | ||||||
| chr10:112970882
|
C | T | 1 | a0001c0001t0014g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.450+6258C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970882 | ||||||
| chr10:112970900
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.450+6276G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970900 | ||||||
| chr10:112970915
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.450+6291C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970915 | ||||||
| chr10:112970996
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.450+6372T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112970996 | ||||||
| chr10:112971038
|
A | G | 99 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(96): Show | 99 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.450+6414A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112971038 | ||||||
| chr10:112971222
|
T | C | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.450+6598T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112971222 | ||||||
| chr10:112971450
|
A | G | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.450+6826A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112971450 | ||||||
| chr10:112971601
|
C | T | 2 | a0001c0001t0002g0100a0001c0001t0002g0108 | 2 | HG01515.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.450+6977C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112971601 | ||||||
| chr10:112971724
|
C | T | 123 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(120): Show | 123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.450+7100C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112971724 | ||||||
| chr10:112971929
|
C | CT | 109 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.450+7314dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112971929 | |||||
| chr10:112972053
|
G | A | 2 | a0001c0001t0014g0153a0003c0003t0020g0135 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.450+7429G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112972053 | ||||||
| chr10:112972548
|
C | A | 109 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(106): Show | 109 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.450+7924C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112972548 | ||||||
| chr10:112972555
|
G | C | 41 | a0001c0001t0001g0129a0001c0001t0002g0006a0001c0001t0002g0012others(38): Show | 41 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.450+7931G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112972555 | ||||||
| chr10:112972593
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.450+7969C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112972593 | ||||||
| chr10:112973123
|
T | C | 143 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(140): Show | 143 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.450+8499T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112973123 | ||||||
| chr10:112973147
|
A | C | 131 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(128): Show | 131 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.450+8523A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112973147 | ||||||
| chr10:112973197
|
G | A | 1 | a0001c0001t0013g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.450+8573G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112973197 | ||||||
| chr10:112973474
|
C | T | 1 | a0001c0001t0004g0016 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.450+8850C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112973474 | ||||||
| chr10:112973578
|
G | GTTTA | 34 | a0001c0001t0001g0062a0001c0001t0001g0130a0001c0001t0001g0131others(31): Show | 34 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.450+8955_450+8958d others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112973578 | |||||
| chr10:112973697
|
C | T | 23 | a0001c0001t0001g0031a0001c0001t0001g0056a0001c0001t0002g0100others(20): Show | 23 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.450+9073C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112973697 | ||||||
| chr10:112973783
|
G | A | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+9159G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112973783 | ||||||
| chr10:112973885
|
C | T | 1 | a0001c0001t0005g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.450+9261C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112973885 | ||||||
| chr10:112974337
|
A | G | 26 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0048others(23): Show | 26 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+9713A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112974337 | ||||||
| chr10:112974734
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | NA19063.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.450+10110C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112974734 | ||||||
| chr10:112974739
|
G | A | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098 | 3 | HG03130.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.450+10115G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112974739 | ||||||
| chr10:112974842
|
A | C | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.450+10218A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112974842 | ||||||
| chr10:112974959
|
T | C | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+10335T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112974959 | ||||||
| chr10:112974984
|
C | CT | 138 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.450+10370dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112974984 | |||||
| chr10:112975076
|
A | G | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0004t0008g0144others(2): Show | 5 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+10452A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975076 | ||||||
| chr10:112975208
|
CAT | C | 3 | a0001c0001t0006g0188a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG01243.hp2 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.450+10587_450+1058 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112975208 | |||||
| chr10:112975306
|
G | C | 21 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(18): Show | 21 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.450+10682G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975306 | ||||||
| chr10:112975351
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.450+10727G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975351 | ||||||
| chr10:112975457
|
A | C | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+10833A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975457 | ||||||
| chr10:112975476
|
T | G | 2 | a0001c0001t0003g0179a0001c0001t0012g0178 | 2 | HG00280.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.450+10852T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975476 | ||||||
| chr10:112975516
|
C | G | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+10892C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975516 | ||||||
| chr10:112975538
|
G | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0079a0001c0001t0028g0014 | 3 | HG02896.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.450+10914G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975538 | ||||||
| chr10:112975683
|
T | C | 42 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0123others(39): Show | 42 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.450+11059T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975683 | ||||||
| chr10:112975762
|
G | A | 49 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.450+11138G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975762 | ||||||
| chr10:112975778
|
G | A | 1 | a0001c0001t0022g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.450+11154G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975778 | ||||||
| chr10:112975963
|
T | C | 6 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(3): Show | 6 | HG02145.hp2 HG02165.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+11339T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112975963 | ||||||
| chr10:112976393
|
G | C | 2 | a0001c0001t0002g0094a0001c0001t0004g0132 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.450+11769G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976393 | ||||||
| chr10:112976486
|
T | G | 1 | a0003c0003t0021g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.450+11862T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976486 | ||||||
| chr10:112976711
|
G | A | 49 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 49 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.450+12087G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976711 | ||||||
| chr10:112976855
|
T | C | 24 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0048others(21): Show | 24 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.450+12231T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976855 | ||||||
| chr10:112976897
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.450+12273G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976897 | ||||||
| chr10:112976911
|
T | G | 6 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+12287T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976911 | ||||||
| chr10:112976914
|
A | G | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0004t0008g0144others(2): Show | 5 | HG01109.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+12290A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976914 | ||||||
| chr10:112976923
|
T | G | 5 | a0001c0001t0004g0016a0001c0001t0004g0097a0001c0001t0024g0121others(2): Show | 5 | HG01884.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+12299T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976923 | ||||||
| chr10:112976975
|
CT | C | 60 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.450+12367delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112976975 | |||||
| chr10:112976991
|
T | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0123others(13): Show | 16 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.450+12367T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112976991 | ||||||
| chr10:112977037
|
C | T | 1 | a0001c0001t0006g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+12413C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977037 | ||||||
| chr10:112977179
|
G | A | 1 | a0001c0001t0007g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.450+12555G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977179 | ||||||
| chr10:112977211
|
G | A | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+12587G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977211 | ||||||
| chr10:112977291
|
C | T | 139 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.450+12667C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977291 | ||||||
| chr10:112977472
|
C | T | 1 | a0001c0001t0003g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.450+12848C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977472 | ||||||
| chr10:112977480
|
A | T | 1 | a0001c0001t0034g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.450+12856A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977480 | ||||||
| chr10:112977510
|
A | C | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.450+12886A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977510 | ||||||
| chr10:112977513
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+12889C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977513 | ||||||
| chr10:112977565
|
C | T | 7 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(4): Show | 7 | HG02145.hp2 HG02165.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+12941C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977565 | ||||||
| chr10:112977566
|
T | C | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.450+12942T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977566 | ||||||
| chr10:112977729
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+13105C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977729 | ||||||
| chr10:112977737
|
A | G | 1 | a0002c0002t0001g0088 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.450+13113A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977737 | ||||||
| chr10:112977771
|
G | A | 1 | a0001c0001t0004g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.450+13147G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977771 | ||||||
| chr10:112977815
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+13191G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977815 | ||||||
| chr10:112977845
|
C | A | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+13221C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112977845 | ||||||
| chr10:112978030
|
G | A | 26 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(23): Show | 26 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+13406G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112978030 | ||||||
| chr10:112978296
|
G | C | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.450+13672G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112978296 | ||||||
| chr10:112978297
|
T | G | 1 | a0001c0001t0011g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.450+13673T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112978297 | ||||||
| chr10:112978469
|
AT | A | 17 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0123others(14): Show | 17 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.450+13859delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112978469 | |||||
| chr10:112978528
|
C | T | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+13904C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112978528 | ||||||
| chr10:112978576
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.450+13952C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112978576 | ||||||
| chr10:112978597
|
G | A | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0133others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+13973G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112978597 | ||||||
| chr10:112978633
|
A | AT | 30 | a0001c0001t0001g0034a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00408.hp1 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.450+14028dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112978633 | |||||
| chr10:112978633
|
AT | A | 25 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(22): Show | 25 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.450+14028delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112978633 | |||||
| chr10:112978702
|
A | C | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+14078A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112978702 | ||||||
| chr10:112979150
|
A | G | 1 | a0001c0001t0029g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.450+14526A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979150 | ||||||
| chr10:112979212
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.450+14588G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979212 | ||||||
| chr10:112979258
|
C | A | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+14634C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979258 | ||||||
| chr10:112979280
|
G | GC | 16 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0123others(13): Show | 16 | HG02109.hp1 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.450+14656_450+1465 others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979280 | ||||||
| chr10:112979293
|
A | G | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+14669A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979293 | ||||||
| chr10:112979407
|
T | G | 1 | a0001c0001t0005g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.450+14783T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979407 | ||||||
| chr10:112979534
|
A | T | 3 | a0001c0001t0011g0175a0001c0001t0011g0184a0001c0001t0014g0055 | 3 | HG01081.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.450+14910A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979534 | ||||||
| chr10:112979756
|
AAAAAAAA others(2): Show |
A | 12 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(9): Show | 12 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.450+15154_450+1516 others(13): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112979756 | |||||
| chr10:112979764
|
A | T | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+15140A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979764 | ||||||
| chr10:112979765
|
T | A | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+15141T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979765 | ||||||
| chr10:112979765
|
T | TA | 24 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0048others(21): Show | 24 | HG00323.hp1 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.450+15149dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112979765 | |||||
| chr10:112979976
|
G | A | 1 | a0001c0001t0004g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.450+15352G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112979976 | ||||||
| chr10:112980228
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+15604C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980228 | ||||||
| chr10:112980538
|
C | T | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+15914C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980538 | ||||||
| chr10:112980662
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.450+16038C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980662 | ||||||
| chr10:112980721
|
G | A | 1 | a0001c0001t0007g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.450+16097G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980721 | ||||||
| chr10:112980750
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.450+16126C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980750 | ||||||
| chr10:112980785
|
C | T | 1 | a0001c0001t0006g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.450+16161C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980785 | ||||||
| chr10:112980858
|
C | T | 131 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.450+16234C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980858 | ||||||
| chr10:112980869
|
G | T | 27 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(24): Show | 27 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.450+16245G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980869 | ||||||
| chr10:112980913
|
A | G | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.450+16289A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980913 | ||||||
| chr10:112980986
|
G | A | 138 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.450+16362G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112980986 | ||||||
| chr10:112981061
|
A | G | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+16437A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112981061 | ||||||
| chr10:112981308
|
C | CA | 7 | a0001c0001t0002g0012a0001c0001t0002g0095a0001c0001t0006g0140others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+16697dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112981308 | |||||
| chr10:112981308
|
CA | C | 136 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.450+16697delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112981308 | |||||
| chr10:112981451
|
C | T | 1 | a0001c0001t0006g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+16827C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112981451 | ||||||
| chr10:112981916
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.450+17292C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112981916 | ||||||
| chr10:112981928
|
A | G | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.450+17304A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112981928 | ||||||
| chr10:112981951
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0123others(1): Show | 4 | HG02818.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+17327G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112981951 | ||||||
| chr10:112982025
|
T | A | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+17401T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982025 | ||||||
| chr10:112982227
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.450+17603T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982227 | ||||||
| chr10:112982234
|
T | A | 6 | a0001c0001t0006g0188a0001c0001t0008g0092a0001c0001t0008g0093others(3): Show | 6 | HG01109.hp2 HG01243.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+17610T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982234 | ||||||
| chr10:112982245
|
A | G | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.450+17621A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982245 | ||||||
| chr10:112982316
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.450+17692G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982316 | ||||||
| chr10:112982334
|
C | T | 2 | a0001c0001t0010g0185a0001c0001t0041g0180 | 2 | HG02293.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.450+17710C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982334 | ||||||
| chr10:112982347
|
G | A | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+17723G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982347 | ||||||
| chr10:112982382
|
C | G | 2 | a0001c0001t0038g0106a0008c0009t0002g0105 | 2 | HG00140.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.450+17758C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982382 | ||||||
| chr10:112982717
|
C | T | 3 | a0001c0001t0006g0188a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG01243.hp2 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.450+18093C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982717 | ||||||
| chr10:112982784
|
C | A | 1 | a0001c0001t0014g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.450+18160C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982784 | ||||||
| chr10:112982786
|
G | A | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.450+18162G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982786 | ||||||
| chr10:112982823
|
C | T | 7 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0006g0007others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+18199C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112982823 | ||||||
| chr10:112983069
|
C | T | 1 | a0001c0004t0008g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.450+18445C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983069 | ||||||
| chr10:112983076
|
G | A | 138 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.450+18452G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983076 | ||||||
| chr10:112983141
|
T | G | 26 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(23): Show | 26 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+18517T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983141 | ||||||
| chr10:112983260
|
A | G | 21 | a0001c0001t0002g0102a0001c0001t0002g0161a0001c0001t0003g0179others(18): Show | 21 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.450+18636A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983260 | ||||||
| chr10:112983308
|
A | G | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+18684A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983308 | ||||||
| chr10:112983332
|
A | G | 7 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(4): Show | 7 | HG02145.hp2 HG02165.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+18708A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983332 | ||||||
| chr10:112983412
|
T | G | 6 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+18788T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983412 | ||||||
| chr10:112983487
|
A | T | 2 | a0001c0001t0037g0160a0001c0004t0013g0145 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.450+18863A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983487 | ||||||
| chr10:112983491
|
A | T | 96 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0038others(93): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.450+18867A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983491 | ||||||
| chr10:112983495
|
T | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.450+18871T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983495 | ||||||
| chr10:112983499
|
T | A | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.450+18875T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983499 | ||||||
| chr10:112983739
|
T | C | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+19115T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983739 | ||||||
| chr10:112983819
|
G | A | 1 | a0001c0001t0009g0057 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.450+19195G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983819 | ||||||
| chr10:112983996
|
G | A | 3 | a0001c0001t0006g0188a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG01243.hp2 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.450+19372G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112983996 | ||||||
| chr10:112984202
|
A | G | 138 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.450+19578A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112984202 | ||||||
| chr10:112984301
|
T | C | 1 | a0001c0001t0005g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.450+19677T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112984301 | ||||||
| chr10:112984310
|
T | G | 11 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0129others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+19686T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112984310 | ||||||
| chr10:112984589
|
T | C | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+19965T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112984589 | ||||||
| chr10:112984694
|
T | G | 48 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.450+20070T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112984694 | ||||||
| chr10:112984778
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.450+20154G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112984778 | ||||||
| chr10:112985000
|
C | T | 1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.450+20376C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112985000 | ||||||
| chr10:112985097
|
GC | G | 4 | a0001c0001t0002g0128a0001c0001t0005g0065a0001c0001t0009g0080others(1): Show | 4 | HG00099.hp2 HG01106.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+20476delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985097 | |||||
| chr10:112985412
|
G | C | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+20788G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112985412 | ||||||
| chr10:112985415
|
AC | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG00408.hp2 HG02683.hp1 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+20796delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985415 | |||||
| chr10:112985482
|
C | CTA | 13 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0125others(10): Show | 13 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+20859_450+2086 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985482 | |||||
| chr10:112985604
|
C | T | 1 | a0001c0001t0025g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.450+20980C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112985604 | ||||||
| chr10:112985858
|
GT | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0194 | 2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.450+21237delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985858 | |||||
| chr10:112985860
|
T | TTG | 17 | a0001c0001t0001g0062a0001c0001t0001g0068a0001c0001t0001g0079others(14): Show | 17 | HG00735.hp2 HG01081.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.450+21267_450+2126 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
T | TTGTG | 11 | a0001c0001t0001g0125a0001c0001t0004g0097a0001c0001t0004g0126others(8): Show | 11 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+21265_450+2126 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
T | TTGTGTG | 6 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0006g0007others(3): Show | 6 | HG01496.hp2 HG02257.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+21263_450+2126 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0086others(7): Show | 10 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.450+21259_450+2126 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0001g0087a0001c0001t0003g0172a0001c0001t0009g0045 | 3 | HG00280.hp1 HG02523.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+21257_450+2126 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.450+21255_450+2126 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0040g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.450+21253_450+2126 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
TTG | T | 37 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0051others(34): Show | 37 | HG00642.hp1 HG00738.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.450+21267_450+2126 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112985860
|
TTGTG | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0004g0076others(4): Show | 7 | HG01243.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+21265_450+2126 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112985860 | |||||
| chr10:112986029
|
G | A | 46 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0099others(43): Show | 46 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.450+21405G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986029 | ||||||
| chr10:112986051
|
T | C | 9 | a0001c0001t0002g0094a0001c0001t0002g0142a0001c0001t0004g0132others(6): Show | 9 | HG01109.hp2 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.450+21427T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986051 | ||||||
| chr10:112986069
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+21445C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986069 | ||||||
| chr10:112986137
|
T | A | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.450+21513T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986137 | ||||||
| chr10:112986281
|
C | G | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.450+21657C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986281 | ||||||
| chr10:112986382
|
G | C | 1 | a0001c0001t0036g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.450+21758G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986382 | ||||||
| chr10:112986821
|
C | G | 111 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0034others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.450+22197C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986821 | ||||||
| chr10:112986915
|
T | C | 2 | a0001c0001t0010g0185a0001c0001t0041g0180 | 2 | HG02293.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.450+22291T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986915 | ||||||
| chr10:112986957
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.450+22333A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986957 | ||||||
| chr10:112986958
|
T | C | 5 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(2): Show | 5 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+22334T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112986958 | ||||||
| chr10:112987106
|
A | T | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.450+22482A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987106 | ||||||
| chr10:112987353
|
A | AATGAT | 3 | a0001c0001t0006g0188a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG01243.hp2 HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.450+22731_450+2273 others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112987353 | |||||
| chr10:112987415
|
G | GT | 45 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.450+22809dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112987415 | |||||
| chr10:112987415
|
GT | G | 47 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0078others(44): Show | 47 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.450+22809delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112987415 | |||||
| chr10:112987415
|
GTT | G | 8 | a0001c0001t0001g0129a0001c0001t0002g0012a0001c0001t0002g0094others(5): Show | 8 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+22808_450+2280 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112987415 | |||||
| chr10:112987433
|
T | C | 11 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0006g0005others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+22809T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987433 | ||||||
| chr10:112987502
|
G | A | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+22878G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987502 | ||||||
| chr10:112987518
|
G | A | 57 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.450+22894G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987518 | ||||||
| chr10:112987617
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.450+22993G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987617 | ||||||
| chr10:112987773
|
C | A | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+23149C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987773 | ||||||
| chr10:112987781
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.450+23157G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987781 | ||||||
| chr10:112987802
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+23178A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987802 | ||||||
| chr10:112987882
|
G | GC | 59 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.450+23258_450+2325 others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987882 | ||||||
| chr10:112987889
|
T | A | 1 | a0001c0001t0001g0036 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.450+23265T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987889 | ||||||
| chr10:112987945
|
G | A | 2 | a0001c0001t0002g0095a0001c0001t0006g0188 | 2 | HG01243.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.450+23321G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112987945 | ||||||
| chr10:112988101
|
C | CGT | 9 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(6): Show | 9 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.450+23490_450+2349 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112988101 | |||||
| chr10:112988252
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+23628C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988252 | ||||||
| chr10:112988270
|
A | T | 57 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(54): Show | 57 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.450+23646A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988270 | ||||||
| chr10:112988346
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0004g0075a0001c0001t0004g0133others(1): Show | 4 | HG02970.hp1 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+23722G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988346 | ||||||
| chr10:112988363
|
T | G | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.450+23739T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988363 | ||||||
| chr10:112988435
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.450+23811T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988435 | ||||||
| chr10:112988553
|
A | C | 3 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0147 | 3 | HG01109.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.450+23929A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988553 | ||||||
| chr10:112988738
|
C | T | 113 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.450+24114C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988738 | ||||||
| chr10:112988799
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.450+24175G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988799 | ||||||
| chr10:112988858
|
G | A | 113 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.450+24234G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988858 | ||||||
| chr10:112988909
|
G | A | 3 | a0001c0001t0005g0033a0001c0001t0016g0023a0004c0006t0001g0039 | 3 | HG02165.hp1 HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.450+24285G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988909 | ||||||
| chr10:112988959
|
G | A | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+24335G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112988959 | ||||||
| chr10:112989259
|
G | A | 7 | a0001c0001t0002g0104a0001c0001t0002g0113a0001c0001t0003g0182others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+24635G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989259 | ||||||
| chr10:112989359
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.450+24735A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989359 | ||||||
| chr10:112989384
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.450+24760C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989384 | ||||||
| chr10:112989426
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.450+24802C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989426 | ||||||
| chr10:112989477
|
G | GA | 21 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(18): Show | 21 | HG01243.hp2 HG02257.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.450+24862dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112989477 | |||||
| chr10:112989662
|
G | A | 11 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(8): Show | 11 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+25038G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989662 | ||||||
| chr10:112989664
|
T | C | 4 | a0001c0001t0004g0097a0001c0001t0013g0103a0001c0001t0024g0121others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+25040T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989664 | ||||||
| chr10:112989739
|
G | C | 4 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0014g0153others(1): Show | 4 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+25115G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989739 | ||||||
| chr10:112989825
|
G | A | 7 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(4): Show | 7 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+25201G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989825 | ||||||
| chr10:112989827
|
T | A | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.450+25203T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989827 | ||||||
| chr10:112989975
|
G | A | 25 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 25 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.450+25351G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112989975 | ||||||
| chr10:112990191
|
A | T | 3 | a0001c0001t0005g0033a0001c0001t0016g0023a0004c0006t0001g0039 | 3 | HG02165.hp1 HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.450+25567A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990191 | ||||||
| chr10:112990224
|
A | G | 2 | a0001c0001t0016g0023a0004c0006t0001g0039 | 2 | HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.450+25600A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990224 | ||||||
| chr10:112990366
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.450+25742G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990366 | ||||||
| chr10:112990398
|
C | T | 48 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(45): Show | 48 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.450+25774C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990398 | ||||||
| chr10:112990477
|
T | C | 26 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.450+25853T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990477 | ||||||
| chr10:112990505
|
G | A | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.450+25881G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990505 | ||||||
| chr10:112990510
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0125others(6): Show | 9 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.450+25886C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990510 | ||||||
| chr10:112990571
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+25947G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990571 | ||||||
| chr10:112990620
|
C | T | 5 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0004g0076others(2): Show | 5 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+25996C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990620 | ||||||
| chr10:112990621
|
G | A | 21 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(18): Show | 21 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.450+25997G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990621 | ||||||
| chr10:112990734
|
T | A | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.450+26110T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990734 | ||||||
| chr10:112990741
|
A | G | 25 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 25 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.450+26117A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990741 | ||||||
| chr10:112990747
|
C | T | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+26123C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990747 | ||||||
| chr10:112990753
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.450+26129A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990753 | ||||||
| chr10:112990771
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.450+26147T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112990771 | ||||||
| chr10:112991079
|
G | A | 2 | a0001c0001t0006g0149a0001c0001t0045g0156 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.450+26455G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991079 | ||||||
| chr10:112991369
|
G | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0002g0095others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+26745G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991369 | ||||||
| chr10:112991400
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.450+26776C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991400 | ||||||
| chr10:112991423
|
G | T | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.450+26799G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991423 | ||||||
| chr10:112991440
|
G | GGAGCTTG others(43): Show |
6 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(3): Show | 6 | HG02895.hp1 HG02897.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+26821_450+2687 others(54): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112991440 | |||||
| chr10:112991526
|
A | G | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.450+26902A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991526 | ||||||
| chr10:112991590
|
C | T | 2 | a0001c0001t0012g0165a0002c0002t0005g0043 | 2 | HG01081.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.450+26966C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991590 | ||||||
| chr10:112991636
|
C | G | 4 | a0001c0001t0008g0148a0001c0001t0011g0159a0001c0001t0037g0160others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+27012C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991636 | ||||||
| chr10:112991694
|
G | A | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+27070G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112991694 | ||||||
| chr10:112992068
|
C | T | 3 | a0001c0001t0002g0142a0001c0001t0006g0149a0001c0001t0045g0156 | 3 | HG02109.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.450+27444C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992068 | ||||||
| chr10:112992181
|
C | T | 5 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(2): Show | 5 | HG02622.hp2 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+27557C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992181 | ||||||
| chr10:112992227
|
G | A | 19 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(16): Show | 19 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+27603G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992227 | ||||||
| chr10:112992299
|
G | A | 11 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0006g0005others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+27675G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992299 | ||||||
| chr10:112992449
|
G | C | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.450+27825G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992449 | ||||||
| chr10:112992453
|
G | A | 4 | a0001c0001t0001g0123a0001c0001t0030g0004a0001c0001t0033g0003others(1): Show | 4 | HG02965.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+27829G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992453 | ||||||
| chr10:112992589
|
C | T | 3 | a0001c0001t0016g0023a0002c0002t0001g0200a0004c0006t0001g0039 | 3 | HG00597.hp1 HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.450+27965C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992589 | ||||||
| chr10:112992594
|
C | G | 1 | a0001c0001t0014g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.450+27970C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992594 | ||||||
| chr10:112992651
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0003g0181 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.450+28027C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992651 | ||||||
| chr10:112992721
|
C | G | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.450+28097C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992721 | ||||||
| chr10:112992734
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0195 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.450+28110C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992734 | ||||||
| chr10:112992744
|
T | C | 25 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 25 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.450+28120T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992744 | ||||||
| chr10:112992794
|
C | T | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.450+28170C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992794 | ||||||
| chr10:112992826
|
C | T | 19 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(16): Show | 19 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+28202C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992826 | ||||||
| chr10:112992915
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0005g0122a0001c0001t0018g0069 | 3 | HG01123.hp1 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.450+28291C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112992915 | ||||||
| chr10:112993045
|
G | A | 1 | a0001c0004t0008g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+28421G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112993045 | ||||||
| chr10:112993454
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+28830C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112993454 | ||||||
| chr10:112993500
|
T | C | 24 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.450+28876T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112993500 | ||||||
| chr10:112993852
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+29228C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112993852 | ||||||
| chr10:112993935
|
G | A | 1 | a0001c0001t0006g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+29311G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112993935 | ||||||
| chr10:112994035
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+29411G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994035 | ||||||
| chr10:112994041
|
C | T | 18 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(15): Show | 18 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.450+29417C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994041 | ||||||
| chr10:112994054
|
C | CA | 52 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.450+29445dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112994054 | |||||
| chr10:112994054
|
C | CAA | 8 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(5): Show | 8 | HG01243.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+29444_450+2944 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112994054 | |||||
| chr10:112994054
|
C | CAAAA | 6 | a0001c0001t0008g0148a0001c0001t0011g0159a0001c0001t0037g0160others(3): Show | 6 | HG02257.hp1 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+29442_450+2944 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112994054 | |||||
| chr10:112994095
|
T | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.450+29471T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994095 | ||||||
| chr10:112994312
|
T | C | 51 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(48): Show | 51 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.450+29688T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994312 | ||||||
| chr10:112994329
|
T | C | 64 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(61): Show | 64 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.450+29705T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994329 | ||||||
| chr10:112994651
|
C | T | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+30027C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994651 | ||||||
| chr10:112994842
|
G | A | 8 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+30218G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994842 | ||||||
| chr10:112994870
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0016g0024 | 2 | HG00408.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.450+30246C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112994870 | ||||||
| chr10:112995025
|
T | C | 49 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(46): Show | 49 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.450+30401T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995025 | ||||||
| chr10:112995094
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+30470T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995094 | ||||||
| chr10:112995199
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+30575C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995199 | ||||||
| chr10:112995403
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.450+30779A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995403 | ||||||
| chr10:112995737
|
G | T | 8 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+31113G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995737 | ||||||
| chr10:112995797
|
C | T | 1 | a0001c0001t0009g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.450+31173C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995797 | ||||||
| chr10:112995930
|
C | G | 3 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0005t0006g0138 | 3 | HG02109.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.450+31306C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995930 | ||||||
| chr10:112995930
|
C | T | 1 | a0001c0001t0022g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.450+31306C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995930 | ||||||
| chr10:112995970
|
C | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0006g0007 | 3 | HG02572.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.450+31346C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995970 | ||||||
| chr10:112995988
|
T | A | 1 | a0001c0001t0001g0078 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.450+31364T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112995988 | ||||||
| chr10:112996236
|
ACT | A | 4 | a0001c0001t0004g0097a0001c0001t0013g0103a0001c0001t0024g0121others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+31616_450+3161 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 112996236 | |||||
| chr10:112996282
|
A | T | 65 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(62): Show | 65 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.450+31658A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996282 | ||||||
| chr10:112996295
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.450+31671C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996295 | ||||||
| chr10:112996365
|
T | C | 1 | a0001c0001t0012g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.450+31741T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996365 | ||||||
| chr10:112996499
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+31875C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996499 | ||||||
| chr10:112996503
|
G | A | 3 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0147 | 3 | HG01109.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.450+31879G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996503 | ||||||
| chr10:112996526
|
G | C | 5 | a0001c0001t0001g0068a0001c0001t0004g0075a0001c0001t0006g0140others(2): Show | 5 | HG02280.hp1 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+31902G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996526 | ||||||
| chr10:112996673
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+32049T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996673 | ||||||
| chr10:112996688
|
G | T | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450+32064G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996688 | ||||||
| chr10:112996700
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.450+32076G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996700 | ||||||
| chr10:112996813
|
A | C | 2 | a0001c0001t0006g0149a0001c0001t0045g0156 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.450+32189A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996813 | ||||||
| chr10:112996935
|
A | G | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.450+32311A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112996935 | ||||||
| chr10:112997018
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+32394G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997018 | ||||||
| chr10:112997047
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+32423C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997047 | ||||||
| chr10:112997080
|
G | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+32456G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997080 | ||||||
| chr10:112997313
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.450+32689T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997313 | ||||||
| chr10:112997314
|
G | T | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.450+32690G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997314 | ||||||
| chr10:112997466
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.450+32842G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997466 | ||||||
| chr10:112997555
|
C | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0078others(5): Show | 8 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+32931C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997555 | ||||||
| chr10:112997639
|
G | C | 2 | a0001c0001t0016g0023a0004c0006t0001g0039 | 2 | HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.450+33015G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997639 | ||||||
| chr10:112997699
|
G | A | 7 | a0001c0001t0001g0129a0001c0001t0002g0012a0001c0001t0002g0155others(4): Show | 7 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+33075G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997699 | ||||||
| chr10:112997777
|
G | C | 1 | a0001c0001t0029g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.450+33153G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997777 | ||||||
| chr10:112997840
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.450+33216T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997840 | ||||||
| chr10:112997946
|
A | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+33322A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112997946 | ||||||
| chr10:112998197
|
C | G | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.450+33573C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112998197 | ||||||
| chr10:112998438
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.450+33814G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112998438 | ||||||
| chr10:112998590
|
C | T | 46 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.450+33966C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112998590 | ||||||
| chr10:112998702
|
G | A | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.450+34078G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112998702 | ||||||
| chr10:112998761
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0002g0012a0001c0001t0002g0155others(4): Show | 7 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+34137C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112998761 | ||||||
| chr10:112998766
|
C | T | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.450+34142C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112998766 | ||||||
| chr10:112998776
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.450+34152A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112998776 | ||||||
| chr10:112999020
|
G | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+34396G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999020 | ||||||
| chr10:112999136
|
C | G | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.450+34512C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999136 | ||||||
| chr10:112999352
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.450+34728G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999352 | ||||||
| chr10:112999425
|
T | C | 7 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(4): Show | 7 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+34801T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999425 | ||||||
| chr10:112999442
|
G | C | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.450+34818G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999442 | ||||||
| chr10:112999600
|
T | C | 2 | a0001c0001t0016g0023a0004c0006t0001g0039 | 2 | HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.450+34976T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999600 | ||||||
| chr10:112999686
|
G | A | 13 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+35062G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999686 | ||||||
| chr10:112999786
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0006g0007 | 3 | HG02572.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.450+35162G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 112999786 | ||||||
| chr10:113000123
|
A | G | 1 | a0001c0001t0013g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.450+35499A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113000123 | ||||||
| chr10:113000459
|
C | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0125others(4): Show | 7 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+35835C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113000459 | ||||||
| chr10:113000525
|
C | T | 13 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+35901C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113000525 | ||||||
| chr10:113000831
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+36207C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113000831 | ||||||
| chr10:113000895
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0006g0188 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.450+36271G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113000895 | ||||||
| chr10:113000918
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0002g0012a0001c0001t0002g0155others(4): Show | 7 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+36294C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113000918 | ||||||
| chr10:113000934
|
A | G | 4 | a0001c0001t0004g0097a0001c0001t0013g0103a0001c0001t0024g0121others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+36310A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113000934 | ||||||
| chr10:113001174
|
G | A | 21 | a0001c0001t0001g0068a0001c0001t0001g0099a0001c0001t0001g0101others(18): Show | 21 | HG02109.hp2 HG02145.hp2 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.450+36550G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001174 | ||||||
| chr10:113001184
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.450+36560G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001184 | ||||||
| chr10:113001228
|
G | A | 2 | a0001c0001t0005g0033a0001c0001t0006g0140 | 2 | HG03942.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.450+36604G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001228 | ||||||
| chr10:113001465
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.450+36841C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001465 | ||||||
| chr10:113001509
|
A | AT | 5 | a0001c0001t0005g0033a0001c0001t0006g0149a0001c0001t0016g0023others(2): Show | 5 | HG02109.hp2 HG02165.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+36896dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113001509 | |||||
| chr10:113001520
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.450+36896T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001520 | ||||||
| chr10:113001737
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.450+37113C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001737 | ||||||
| chr10:113001938
|
A | C | 119 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.450+37314A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001938 | ||||||
| chr10:113001960
|
G | A | 14 | a0001c0001t0001g0068a0001c0001t0001g0099a0001c0001t0001g0101others(11): Show | 14 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.450+37336G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113001960 | ||||||
| chr10:113002131
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.450+37507G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113002131 | ||||||
| chr10:113002237
|
G | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.450+37613G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113002237 | ||||||
| chr10:113002305
|
G | T | 119 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.450+37681G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113002305 | ||||||
| chr10:113002478
|
G | A | 118 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.451-37547G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113002478 | ||||||
| chr10:113002774
|
A | T | 2 | a0001c0001t0004g0075a0001c0001t0006g0013 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.451-37251A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113002774 | ||||||
| chr10:113002784
|
C | T | 5 | a0001c0001t0001g0066a0001c0001t0002g0142a0001c0004t0008g0144others(2): Show | 5 | HG01109.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-37241C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113002784 | ||||||
| chr10:113002796
|
A | G | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-37229A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113002796 | ||||||
| chr10:113003247
|
G | A | 1 | a0002c0002t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.451-36778G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113003247 | ||||||
| chr10:113003531
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0002g0006 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.451-36494C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113003531 | ||||||
| chr10:113003532
|
A | G | 1 | a0001c0001t0003g0163 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.451-36493A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113003532 | ||||||
| chr10:113003574
|
G | A | 2 | a0001c0001t0016g0023a0004c0006t0001g0039 | 2 | HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.451-36451G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113003574 | ||||||
| chr10:113003655
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0006g0007others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-36370A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113003655 | ||||||
| chr10:113003763
|
G | T | 2 | a0001c0001t0016g0023a0004c0006t0001g0039 | 2 | HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.451-36262G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113003763 | ||||||
| chr10:113003800
|
C | T | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-36225C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113003800 | ||||||
| chr10:113004074
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.451-35951C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113004074 | ||||||
| chr10:113004101
|
C | A | 2 | a0001c0001t0001g0061a0001c0001t0034g0187 | 2 | HG01496.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-35924C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113004101 | ||||||
| chr10:113004246
|
A | G | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.451-35779A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113004246 | ||||||
| chr10:113004262
|
G | A | 3 | a0001c0001t0002g0128a0001c0001t0005g0065a0001c0001t0009g0081 | 3 | HG00099.hp2 HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.451-35763G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113004262 | ||||||
| chr10:113004860
|
G | T | 3 | a0001c0001t0001g0086a0001c0001t0003g0172a0001c0001t0038g0106 | 3 | HG01981.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.451-35165G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113004860 | ||||||
| chr10:113004874
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-35151G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113004874 | ||||||
| chr10:113004902
|
G | A | 116 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0034others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.451-35123G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113004902 | ||||||
| chr10:113005046
|
C | T | 1 | a0001c0001t0011g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.451-34979C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005046 | ||||||
| chr10:113005179
|
G | A | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-34846G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005179 | ||||||
| chr10:113005200
|
C | G | 15 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(12): Show | 15 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.451-34825C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005200 | ||||||
| chr10:113005412
|
G | A | 118 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.451-34613G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005412 | ||||||
| chr10:113005467
|
T | C | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-34558T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005467 | ||||||
| chr10:113005614
|
A | C | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.451-34411A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005614 | ||||||
| chr10:113005631
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0002g0096 | 2 | HG01255.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.451-34394G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005631 | ||||||
| chr10:113005700
|
G | A | 2 | a0001c0001t0011g0175a0001c0001t0011g0184 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.451-34325G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005700 | ||||||
| chr10:113005701
|
G | T | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-34324G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005701 | ||||||
| chr10:113005710
|
G | T | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-34315G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005710 | ||||||
| chr10:113005988
|
C | A | 83 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(80): Show | 83 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.451-34037C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113005988 | ||||||
| chr10:113006159
|
C | T | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-33866C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113006159 | ||||||
| chr10:113006209
|
G | GA | 8 | a0001c0001t0002g0104a0001c0001t0002g0113a0001c0001t0003g0182others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-33814dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113006209 | |||||
| chr10:113006483
|
T | C | 1 | a0002c0002t0018g0022 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.451-33542T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113006483 | ||||||
| chr10:113006908
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.451-33117C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113006908 | ||||||
| chr10:113006958
|
C | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(25): Show | 28 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.451-33067C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113006958 | ||||||
| chr10:113007035
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.451-32990C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113007035 | ||||||
| chr10:113007230
|
C | T | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.451-32795C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113007230 | ||||||
| chr10:113007456
|
C | G | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-32569C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113007456 | ||||||
| chr10:113007657
|
T | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0006g0007 | 3 | HG02572.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-32368T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113007657 | ||||||
| chr10:113007701
|
C | G | 1 | a0001c0001t0013g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.451-32324C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113007701 | ||||||
| chr10:113007851
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.451-32174G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113007851 | ||||||
| chr10:113007990
|
C | T | 199 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.451-32035C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113007990 | ||||||
| chr10:113008012
|
G | A | 86 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(83): Show | 86 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.451-32013G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008012 | ||||||
| chr10:113008129
|
T | G | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451-31896T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008129 | ||||||
| chr10:113008262
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.451-31763C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008262 | ||||||
| chr10:113008332
|
C | T | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-31693C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008332 | ||||||
| chr10:113008550
|
G | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-31475G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008550 | ||||||
| chr10:113008695
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.451-31330G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008695 | ||||||
| chr10:113008850
|
A | G | 120 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(117): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.451-31175A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008850 | ||||||
| chr10:113008899
|
A | G | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-31126A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008899 | ||||||
| chr10:113008957
|
T | C | 2 | a0001c0001t0016g0023a0004c0006t0001g0039 | 2 | HG02165.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.451-31068T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113008957 | ||||||
| chr10:113009023
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-31002C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113009023 | ||||||
| chr10:113009024
|
G | A | 112 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.451-31001G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113009024 | ||||||
| chr10:113009254
|
C | T | 2 | a0001c0001t0008g0139a0001c0001t0010g0127 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.451-30771C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113009254 | ||||||
| chr10:113009647
|
T | G | 3 | a0001c0001t0001g0068a0001c0001t0004g0075a0001c0001t0006g0013 | 3 | HG02258.hp1 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.451-30378T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113009647 | ||||||
| chr10:113009679
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.451-30346G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113009679 | ||||||
| chr10:113010220
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-29805G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113010220 | ||||||
| chr10:113010387
|
C | T | 12 | a0001c0001t0001g0130a0001c0001t0002g0142a0001c0001t0004g0134others(9): Show | 12 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-29638C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113010387 | ||||||
| chr10:113010440
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-29585G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113010440 | ||||||
| chr10:113010885
|
G | A | 1 | a0001c0001t0017g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.451-29140G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113010885 | ||||||
| chr10:113010886
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0016g0024 | 2 | HG00408.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.451-29139T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113010886 | ||||||
| chr10:113011339
|
G | T | 11 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0008g0139others(8): Show | 11 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-28686G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113011339 | ||||||
| chr10:113011344
|
G | C | 2 | a0001c0001t0004g0016a0001c0001t0004g0133 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-28681G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113011344 | ||||||
| chr10:113011401
|
C | G | 2 | a0001c0001t0004g0075a0001c0001t0006g0013 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.451-28624C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113011401 | ||||||
| chr10:113011523
|
C | T | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-28502C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113011523 | ||||||
| chr10:113011524
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-28501C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113011524 | ||||||
| chr10:113011639
|
GTATTACT others(21): Show |
G | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.451-28376_451-2834 others(32): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113011639 | |||||
| chr10:113011906
|
G | A | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-28119G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113011906 | ||||||
| chr10:113012084
|
A | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(25): Show | 28 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.451-27941A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012084 | ||||||
| chr10:113012194
|
T | TG | 5 | a0001c0001t0001g0049a0001c0001t0001g0190a0001c0001t0001g0193others(2): Show | 5 | HG02735.hp1 HG02735.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-27827dupG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113012194 | |||||
| chr10:113012204
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0008g0139others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-27821G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012204 | ||||||
| chr10:113012413
|
G | A | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.451-27612G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012413 | ||||||
| chr10:113012494
|
C | CA | 119 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.451-27528dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113012494 | |||||
| chr10:113012547
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.451-27478C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012547 | ||||||
| chr10:113012670
|
G | A | 2 | a0001c0001t0003g0174a0001c0001t0010g0185 | 2 | HG02293.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.451-27355G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012670 | ||||||
| chr10:113012830
|
C | G | 2 | a0001c0001t0005g0033a0004c0006t0001g0039 | 2 | HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.451-27195C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012830 | ||||||
| chr10:113012911
|
C | T | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.451-27114C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012911 | ||||||
| chr10:113012961
|
G | C | 199 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.451-27064G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012961 | ||||||
| chr10:113012987
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-27038C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113012987 | ||||||
| chr10:113013114
|
G | GT | 12 | a0001c0001t0001g0038a0001c0001t0001g0195a0001c0001t0002g0102others(9): Show | 12 | HG00438.hp1 HG00738.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.451-26889dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113013114 | |||||
| chr10:113013114
|
GT | G | 27 | a0001c0001t0001g0041a0001c0001t0001g0061a0001c0001t0001g0125others(24): Show | 27 | HG00642.hp2 HG00735.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.451-26889delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113013114 | |||||
| chr10:113013114
|
GTT | G | 86 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.451-26890_451-2688 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113013114 | |||||
| chr10:113013114
|
GTTT | G | 5 | a0001c0001t0001g0062a0001c0001t0006g0007a0001c0001t0008g0092others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-26891_451-2688 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113013114 | |||||
| chr10:113013119
|
T | G | 1 | a0001c0001t0014g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.451-26906T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013119 | ||||||
| chr10:113013264
|
G | A | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.451-26761G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013264 | ||||||
| chr10:113013275
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.451-26750C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013275 | ||||||
| chr10:113013309
|
G | T | 29 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0047others(26): Show | 29 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.451-26716G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013309 | ||||||
| chr10:113013594
|
G | A | 1 | a0001c0001t0025g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.451-26431G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013594 | ||||||
| chr10:113013664
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.451-26361A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013664 | ||||||
| chr10:113013756
|
C | T | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.451-26269C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013756 | ||||||
| chr10:113013849
|
A | G | 24 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.451-26176A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013849 | ||||||
| chr10:113013990
|
T | A | 1 | a0001c0013t0027g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.451-26035T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113013990 | ||||||
| chr10:113014001
|
A | T | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-26024A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113014001 | ||||||
| chr10:113014167
|
C | T | 63 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(60): Show | 63 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.451-25858C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113014167 | ||||||
| chr10:113014168
|
A | G | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-25857A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113014168 | ||||||
| chr10:113014240
|
C | T | 1 | a0001c0001t0003g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.451-25785C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113014240 | ||||||
| chr10:113014554
|
A | AG | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.451-25469dupG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113014554 | |||||
| chr10:113014613
|
C | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0006g0005others(5): Show | 8 | HG02055.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-25412C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113014613 | ||||||
| chr10:113014674
|
A | C | 48 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(45): Show | 48 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.451-25351A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113014674 | ||||||
| chr10:113015070
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.451-24955C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015070 | ||||||
| chr10:113015384
|
C | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0197a0002c0002t0001g0021others(1): Show | 4 | HG02132.hp1 NA18964.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-24641C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015384 | ||||||
| chr10:113015446
|
C | CT | 6 | a0001c0001t0003g0186a0001c0001t0012g0165a0001c0001t0014g0083others(3): Show | 6 | HG00597.hp1 HG01346.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-24558dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113015446 | |||||
| chr10:113015446
|
CT | C | 100 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(97): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.451-24558delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113015446 | |||||
| chr10:113015476
|
G | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.451-24549G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015476 | ||||||
| chr10:113015624
|
C | T | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-24401C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015624 | ||||||
| chr10:113015653
|
T | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0004g0076others(2): Show | 5 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-24372T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015653 | ||||||
| chr10:113015855
|
G | A | 1 | a0008c0009t0002g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.451-24170G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015855 | ||||||
| chr10:113015952
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0004g0132a0001c0001t0005g0054 | 3 | HG02622.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.451-24073A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015952 | ||||||
| chr10:113015966
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.451-24059G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113015966 | ||||||
| chr10:113016063
|
AT | A | 85 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(82): Show | 85 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.451-23947delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113016063 | |||||
| chr10:113016614
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0016g0024 | 2 | HG00408.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.451-23411G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113016614 | ||||||
| chr10:113016698
|
G | A | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-23327G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113016698 | ||||||
| chr10:113017187
|
T | G | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-22838T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017187 | ||||||
| chr10:113017364
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0006g0007 | 3 | HG02572.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-22661G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017364 | ||||||
| chr10:113017379
|
CAGTGGTG others(1): Show |
C | 112 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.451-22643_451-2263 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113017379 | |||||
| chr10:113017637
|
C | T | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-22388C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017637 | ||||||
| chr10:113017638
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.451-22387G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017638 | ||||||
| chr10:113017873
|
G | C | 1 | a0001c0001t0023g0027 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.451-22152G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017873 | ||||||
| chr10:113017898
|
G | A | 8 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0008g0139others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-22127G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017898 | ||||||
| chr10:113017911
|
C | T | 111 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.451-22114C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017911 | ||||||
| chr10:113017965
|
A | G | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-22060A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113017965 | ||||||
| chr10:113018444
|
C | CT | 48 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(45): Show | 48 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.451-21556dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113018444 | |||||
| chr10:113018444
|
C | CTT | 62 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.451-21557_451-2155 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113018444 | |||||
| chr10:113018444
|
C | CTTT | 6 | a0001c0001t0001g0041a0001c0001t0002g0006a0001c0001t0002g0095others(3): Show | 6 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-21558_451-2155 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113018444 | |||||
| chr10:113018444
|
CT | C | 6 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0060others(3): Show | 6 | HG00323.hp2 HG01256.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-21556delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113018444 | |||||
| chr10:113018493
|
A | G | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-21532A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018493 | ||||||
| chr10:113018552
|
A | G | 3 | a0001c0001t0001g0087a0002c0002t0001g0088a0005c0010t0003g0167 | 3 | HG00597.hp2 HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.451-21473A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018552 | ||||||
| chr10:113018641
|
T | C | 1 | a0001c0001t0012g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.451-21384T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018641 | ||||||
| chr10:113018723
|
C | G | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-21302C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018723 | ||||||
| chr10:113018734
|
C | T | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.451-21291C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018734 | ||||||
| chr10:113018747
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-21278C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018747 | ||||||
| chr10:113018842
|
G | A | 3 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0147 | 3 | HG01109.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.451-21183G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018842 | ||||||
| chr10:113018980
|
C | A | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-21045C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113018980 | ||||||
| chr10:113019200
|
G | A | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.451-20825G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113019200 | ||||||
| chr10:113019219
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0078 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.451-20806G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113019219 | ||||||
| chr10:113019254
|
C | T | 12 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(9): Show | 12 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-20771C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113019254 | ||||||
| chr10:113019553
|
T | C | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-20472T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113019553 | ||||||
| chr10:113019652
|
CA | C | 13 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-20364delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113019652 | |||||
| chr10:113019779
|
G | A | 116 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.451-20246G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113019779 | ||||||
| chr10:113019798
|
ATT | A | 116 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.451-20215_451-2021 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113019798 | |||||
| chr10:113019896
|
C | T | 1 | a0002c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.451-20129C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113019896 | ||||||
| chr10:113020075
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.451-19950G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113020075 | ||||||
| chr10:113020565
|
T | C | 3 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0147 | 3 | HG01109.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.451-19460T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113020565 | ||||||
| chr10:113020874
|
A | C | 118 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.451-19151A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113020874 | ||||||
| chr10:113020891
|
G | A | 4 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-19134G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113020891 | ||||||
| chr10:113021014
|
C | A | 1 | a0001c0001t0005g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.451-19011C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021014 | ||||||
| chr10:113021064
|
G | T | 3 | a0001c0001t0002g0173a0001c0001t0041g0180a0002c0002t0003g0171 | 3 | HG01978.hp2 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.451-18961G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021064 | ||||||
| chr10:113021194
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.451-18831C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021194 | ||||||
| chr10:113021473
|
A | T | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-18552A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021473 | ||||||
| chr10:113021538
|
A | C | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-18487A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021538 | ||||||
| chr10:113021637
|
C | A | 6 | a0001c0001t0001g0068a0001c0001t0004g0075a0001c0001t0006g0013others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-18388C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021637 | ||||||
| chr10:113021641
|
C | A | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-18384C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021641 | ||||||
| chr10:113021643
|
A | C | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-18382A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021643 | ||||||
| chr10:113021939
|
T | C | 118 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(115): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.451-18086T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113021939 | ||||||
| chr10:113022063
|
T | A | 10 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-17962T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022063 | ||||||
| chr10:113022104
|
T | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(9): Show | 12 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-17921T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022104 | ||||||
| chr10:113022191
|
G | C | 21 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(18): Show | 21 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.451-17834G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022191 | ||||||
| chr10:113022333
|
A | T | 1 | a0001c0001t0012g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.451-17692A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022333 | ||||||
| chr10:113022352
|
A | G | 1 | a0001c0001t0009g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.451-17673A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022352 | ||||||
| chr10:113022528
|
T | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(9): Show | 12 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-17497T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022528 | ||||||
| chr10:113022531
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0002g0096 | 2 | HG01255.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.451-17494G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022531 | ||||||
| chr10:113022590
|
C | T | 1 | a0001c0001t0009g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.451-17435C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022590 | ||||||
| chr10:113022793
|
C | T | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.451-17232C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022793 | ||||||
| chr10:113022822
|
G | GCT | 41 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(38): Show | 41 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.451-17203_451-1720 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022822 | ||||||
| chr10:113022835
|
A | C | 4 | a0001c0001t0002g0142a0001c0004t0008g0144a0001c0004t0008g0146others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-17190A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022835 | ||||||
| chr10:113022967
|
T | A | 1 | a0001c0001t0009g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.451-17058T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113022967 | ||||||
| chr10:113023031
|
G | T | 24 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.451-16994G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023031 | ||||||
| chr10:113023044
|
T | C | 111 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.451-16981T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023044 | ||||||
| chr10:113023126
|
G | A | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.451-16899G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023126 | ||||||
| chr10:113023143
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-16882C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023143 | ||||||
| chr10:113023325
|
G | A | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.451-16700G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023325 | ||||||
| chr10:113023339
|
A | G | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.451-16686A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023339 | ||||||
| chr10:113023574
|
C | T | 113 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.451-16451C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023574 | ||||||
| chr10:113023644
|
C | G | 116 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.451-16381C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023644 | ||||||
| chr10:113023827
|
C | G | 111 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.451-16198C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023827 | ||||||
| chr10:113023877
|
C | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-16148C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113023877 | ||||||
| chr10:113024016
|
T | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(25): Show | 28 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.451-16009T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024016 | ||||||
| chr10:113024033
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-15992C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024033 | ||||||
| chr10:113024079
|
T | C | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-15946T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024079 | ||||||
| chr10:113024128
|
T | G | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-15897T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024128 | ||||||
| chr10:113024289
|
G | A | 1 | a0007c0008t0002g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.451-15736G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024289 | ||||||
| chr10:113024308
|
AAAAC | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0006g0007 | 3 | HG02572.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-15697_451-1569 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113024308 | |||||
| chr10:113024389
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.451-15636T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024389 | ||||||
| chr10:113024466
|
A | G | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.451-15559A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024466 | ||||||
| chr10:113024495
|
T | C | 5 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-15530T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024495 | ||||||
| chr10:113024548
|
C | T | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-15477C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024548 | ||||||
| chr10:113024616
|
C | CT | 24 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.451-15389dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113024616 | |||||
| chr10:113024616
|
CT | C | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0010g0098others(2): Show | 5 | HG02683.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-15389delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113024616 | |||||
| chr10:113024636
|
TG | T | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(25): Show | 28 | HG00280.hp2 HG01258.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.451-15388delG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024636 | ||||||
| chr10:113024637
|
G | T | 10 | a0001c0001t0001g0074a0001c0001t0001g0125a0001c0001t0002g0104others(7): Show | 10 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-15388G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024637 | ||||||
| chr10:113024688
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.451-15337C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024688 | ||||||
| chr10:113024776
|
C | A | 2 | a0001c0001t0003g0174a0001c0001t0010g0185 | 2 | HG02293.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.451-15249C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024776 | ||||||
| chr10:113024840
|
G | A | 1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.451-15185G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024840 | ||||||
| chr10:113024843
|
C | T | 10 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-15182C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024843 | ||||||
| chr10:113024913
|
A | G | 1 | a0001c0001t0012g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.451-15112A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024913 | ||||||
| chr10:113024975
|
C | G | 1 | a0001c0001t0003g0163 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.451-15050C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113024975 | ||||||
| chr10:113025023
|
G | A | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.451-15002G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025023 | ||||||
| chr10:113025167
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.451-14858C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025167 | ||||||
| chr10:113025218
|
AT | A | 102 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(99): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.451-14784delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113025218 | |||||
| chr10:113025300
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.451-14725G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025300 | ||||||
| chr10:113025411
|
G | A | 1 | a0002c0002t0003g0171 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.451-14614G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025411 | ||||||
| chr10:113025428
|
G | A | 1 | a0001c0001t0005g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.451-14597G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025428 | ||||||
| chr10:113025519
|
A | G | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-14506A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025519 | ||||||
| chr10:113025533
|
C | T | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-14492C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025533 | ||||||
| chr10:113025651
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-14374G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025651 | ||||||
| chr10:113025665
|
G | A | 46 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.451-14360G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025665 | ||||||
| chr10:113025670
|
C | T | 1 | a0001c0001t0006g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.451-14355C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025670 | ||||||
| chr10:113025753
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-14272T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025753 | ||||||
| chr10:113025816
|
T | G | 2 | a0001c0001t0001g0089a0001c0001t0002g0161 | 2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.451-14209T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025816 | ||||||
| chr10:113025880
|
A | AT | 26 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.451-14129dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113025880 | |||||
| chr10:113025918
|
C | T | 8 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0078others(5): Show | 8 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-14107C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113025918 | ||||||
| chr10:113026024
|
A | G | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.451-14001A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026024 | ||||||
| chr10:113026075
|
C | T | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-13950C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026075 | ||||||
| chr10:113026126
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0002g0006a0001c0001t0015g0008 | 3 | HG02809.hp1 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.451-13899A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026126 | ||||||
| chr10:113026142
|
G | A | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.451-13883G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026142 | ||||||
| chr10:113026165
|
C | T | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.451-13860C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026165 | ||||||
| chr10:113026180
|
A | G | 116 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.451-13845A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026180 | ||||||
| chr10:113026255
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-13770G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026255 | ||||||
| chr10:113026320
|
T | G | 1 | a0001c0001t0002g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.451-13705T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026320 | ||||||
| chr10:113026343
|
T | G | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-13682T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026343 | ||||||
| chr10:113026395
|
A | G | 116 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.451-13630A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113026395 | ||||||
| chr10:113027124
|
A | G | 3 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0147 | 3 | HG01109.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.451-12901A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027124 | ||||||
| chr10:113027165
|
G | A | 1 | a0002c0002t0005g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.451-12860G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027165 | ||||||
| chr10:113027253
|
T | C | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-12772T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027253 | ||||||
| chr10:113027293
|
G | A | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-12732G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027293 | ||||||
| chr10:113027331
|
A | G | 117 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.451-12694A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027331 | ||||||
| chr10:113027350
|
G | A | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.451-12675G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027350 | ||||||
| chr10:113027399
|
T | C | 1 | a0001c0001t0025g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.451-12626T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027399 | ||||||
| chr10:113027404
|
T | G | 3 | a0001c0001t0001g0086a0001c0001t0003g0172a0001c0001t0038g0106 | 3 | HG01981.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.451-12621T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027404 | ||||||
| chr10:113027525
|
A | G | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.451-12500A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027525 | ||||||
| chr10:113027783
|
C | A | 1 | a0004c0006t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-12242C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027783 | ||||||
| chr10:113027885
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451-12140G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027885 | ||||||
| chr10:113027967
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.451-12058G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113027967 | ||||||
| chr10:113028189
|
G | A | 1 | a0002c0002t0010g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.451-11836G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028189 | ||||||
| chr10:113028220
|
G | A | 1 | a0001c0001t0015g0008 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.451-11805G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028220 | ||||||
| chr10:113028352
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.451-11673G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028352 | ||||||
| chr10:113028431
|
T | TG | 17 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(14): Show | 17 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.451-11591dupG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113028431 | |||||
| chr10:113028564
|
A | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-11461A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028564 | ||||||
| chr10:113028577
|
G | T | 1 | a0001c0001t0011g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.451-11448G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028577 | ||||||
| chr10:113028579
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.451-11446G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028579 | ||||||
| chr10:113028580
|
C | A | 1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.451-11445C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028580 | ||||||
| chr10:113028677
|
C | T | 23 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(20): Show | 23 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.451-11348C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028677 | ||||||
| chr10:113028811
|
G | C | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.451-11214G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028811 | ||||||
| chr10:113028927
|
G | C | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-11098G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028927 | ||||||
| chr10:113028970
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-11055G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113028970 | ||||||
| chr10:113029056
|
T | C | 58 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(55): Show | 58 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.451-10969T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029056 | ||||||
| chr10:113029126
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0002g0006 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.451-10899T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029126 | ||||||
| chr10:113029260
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0006g0157 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.451-10765C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029260 | ||||||
| chr10:113029313
|
T | G | 1 | a0003c0003t0032g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.451-10712T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029313 | ||||||
| chr10:113029318
|
T | C | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.451-10707T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029318 | ||||||
| chr10:113029341
|
C | T | 10 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-10684C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029341 | ||||||
| chr10:113029511
|
T | C | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-10514T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029511 | ||||||
| chr10:113029524
|
C | CT | 14 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0066others(11): Show | 14 | HG00099.hp1 HG02132.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.451-10482dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113029524 | |||||
| chr10:113029524
|
CT | C | 10 | a0001c0001t0001g0131a0001c0001t0002g0095a0001c0001t0004g0016others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-10482delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113029524 | |||||
| chr10:113029636
|
C | T | 1 | a0002c0002t0003g0171 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.451-10389C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029636 | ||||||
| chr10:113029750
|
A | G | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.451-10275A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029750 | ||||||
| chr10:113029786
|
C | T | 1 | a0001c0001t0025g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.451-10239C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029786 | ||||||
| chr10:113029818
|
C | T | 1 | a0001c0001t0025g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.451-10207C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113029818 | ||||||
| chr10:113030162
|
A | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-9863A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113030162 | ||||||
| chr10:113030291
|
C | T | 1 | a0001c0001t0005g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.451-9734C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113030291 | ||||||
| chr10:113030314
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.451-9711G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113030314 | ||||||
| chr10:113030349
|
C | T | 4 | a0001c0001t0001g0044a0001c0001t0003g0179a0001c0001t0005g0072others(1): Show | 4 | HG00280.hp1 HG01106.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-9676C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113030349 | ||||||
| chr10:113030649
|
C | T | 2 | a0001c0001t0001g0018a0002c0002t0003g0162 | 2 | NA19063.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.451-9376C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113030649 | ||||||
| chr10:113030933
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-9092C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113030933 | ||||||
| chr10:113031049
|
C | T | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.451-8976C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031049 | ||||||
| chr10:113031052
|
A | G | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-8973A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031052 | ||||||
| chr10:113031457
|
GC | G | 2 | a0001c0001t0014g0153a0003c0003t0020g0135 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.451-8567delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031457 | ||||||
| chr10:113031480
|
CT | C | 65 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0034others(62): Show | 65 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.451-8526delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113031480 | |||||
| chr10:113031480
|
CTT | C | 12 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0078others(9): Show | 12 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-8527_451-8526d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113031480 | |||||
| chr10:113031612
|
C | T | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.451-8413C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031612 | ||||||
| chr10:113031624
|
A | G | 5 | a0001c0001t0001g0123a0001c0001t0009g0080a0001c0001t0030g0004others(2): Show | 5 | HG02965.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-8401A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031624 | ||||||
| chr10:113031629
|
A | G | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.451-8396A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031629 | ||||||
| chr10:113031662
|
A | G | 1 | a0001c0001t0002g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.451-8363A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031662 | ||||||
| chr10:113031703
|
G | T | 1 | a0001c0001t0005g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.451-8322G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031703 | ||||||
| chr10:113031707
|
C | G | 1 | a0001c0001t0008g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.451-8318C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031707 | ||||||
| chr10:113031731
|
C | T | 51 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(48): Show | 51 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.451-8294C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113031731 | ||||||
| chr10:113032012
|
G | C | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-8013G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032012 | ||||||
| chr10:113032036
|
G | C | 2 | a0001c0001t0006g0005a0007c0008t0002g0015 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.451-7989G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032036 | ||||||
| chr10:113032097
|
T | A | 1 | a0001c0001t0022g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.451-7928T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032097 | ||||||
| chr10:113032125
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-7900C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032125 | ||||||
| chr10:113032328
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.451-7697C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032328 | ||||||
| chr10:113032340
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-7685A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032340 | ||||||
| chr10:113032380
|
T | C | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.451-7645T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032380 | ||||||
| chr10:113032556
|
A | G | 8 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-7469A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032556 | ||||||
| chr10:113032591
|
G | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-7434G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032591 | ||||||
| chr10:113032709
|
C | T | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.451-7316C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032709 | ||||||
| chr10:113032759
|
C | G | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.451-7266C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032759 | ||||||
| chr10:113032773
|
G | A | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.451-7252G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032773 | ||||||
| chr10:113032808
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.451-7217G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032808 | ||||||
| chr10:113032960
|
A | G | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-7065A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113032960 | ||||||
| chr10:113033125
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.451-6900C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033125 | ||||||
| chr10:113033181
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-6844T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033181 | ||||||
| chr10:113033203
|
TTCC | T | 7 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-6811_451-6809d others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113033203 | |||||
| chr10:113033238
|
T | C | 2 | a0001c0001t0002g0108a0001c0001t0003g0181 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.451-6787T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033238 | ||||||
| chr10:113033339
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-6686A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033339 | ||||||
| chr10:113033405
|
C | T | 3 | a0001c0001t0005g0033a0002c0002t0003g0171a0004c0006t0001g0039 | 3 | HG01978.hp2 HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.451-6620C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033405 | ||||||
| chr10:113033432
|
T | C | 7 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-6593T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033432 | ||||||
| chr10:113033478
|
A | G | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.451-6547A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033478 | ||||||
| chr10:113033633
|
C | A | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.451-6392C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033633 | ||||||
| chr10:113033692
|
G | A | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.451-6333G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033692 | ||||||
| chr10:113033813
|
T | C | 2 | a0001c0001t0002g0143a0001c0001t0012g0169 | 2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.451-6212T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113033813 | ||||||
| chr10:113034019
|
T | C | 1 | a0001c0001t0034g0187 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.451-6006T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034019 | ||||||
| chr10:113034064
|
T | A | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.451-5961T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034064 | ||||||
| chr10:113034148
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.451-5877T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034148 | ||||||
| chr10:113034331
|
G | A | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451-5694G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034331 | ||||||
| chr10:113034370
|
G | A | 2 | a0001c0001t0003g0179a0001c0001t0009g0045 | 2 | HG00280.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.451-5655G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034370 | ||||||
| chr10:113034852
|
C | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0009g0080others(4): Show | 7 | HG02717.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.451-5173C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034852 | ||||||
| chr10:113034960
|
C | T | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.451-5065C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034960 | ||||||
| chr10:113034965
|
CTCCTTCC others(13): Show |
C | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-5046_451-5027d others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113034965 | |||||
| chr10:113034972
|
C | G | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451-5053C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113034972 | ||||||
| chr10:113035120
|
A | G | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.451-4905A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113035120 | ||||||
| chr10:113035169
|
C | A | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-4856C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113035169 | ||||||
| chr10:113035183
|
T | A | 1 | a0001c0001t0003g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.451-4842T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113035183 | ||||||
| chr10:113035331
|
C | G | 2 | a0001c0001t0004g0016a0001c0001t0004g0133 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-4694C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113035331 | ||||||
| chr10:113035497
|
G | C | 23 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(20): Show | 23 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.451-4528G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113035497 | ||||||
| chr10:113035587
|
A | C | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-4438A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113035587 | ||||||
| chr10:113035837
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.451-4188A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113035837 | ||||||
| chr10:113036115
|
CCAT | C | 58 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0038others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.451-3863_451-3861d others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036115 | |||||
| chr10:113036115
|
CCATCAT | C | 31 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0087others(28): Show | 31 | HG00323.hp2 HG00438.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.451-3866_451-3861d others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036115 | |||||
| chr10:113036115
|
CCATCATC others(2): Show |
C | 66 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.451-3869_451-3861d others(11): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036115 | |||||
| chr10:113036115
|
CCATCATC others(5): Show |
C | 16 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 16 | HG00642.hp2 HG00738.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-3872_451-3861d others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036115 | |||||
| chr10:113036115
|
CCATCATC others(8): Show |
C | 7 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0004g0126others(4): Show | 7 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.451-3875_451-3861d others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036115 | |||||
| chr10:113036115
|
CCATCATC others(11): Show |
C | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-3878_451-3861d others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036115 | |||||
| chr10:113036126
|
A | C | 1 | a0001c0001t0040g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.451-3899A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036126 | ||||||
| chr10:113036133
|
T | C | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451-3892T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036133 | ||||||
| chr10:113036244
|
G | A | 11 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0060others(8): Show | 11 | HG00438.hp1 HG00597.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.451-3781G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036244 | ||||||
| chr10:113036289
|
A | G | 112 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.451-3736A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036289 | ||||||
| chr10:113036354
|
G | C | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.451-3671G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036354 | ||||||
| chr10:113036358
|
A | G | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.451-3667A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036358 | ||||||
| chr10:113036506
|
C | T | 1 | a0001c0001t0025g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.451-3519C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036506 | ||||||
| chr10:113036575
|
T | C | 2 | a0001c0001t0011g0175a0001c0001t0011g0184 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.451-3450T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036575 | ||||||
| chr10:113036665
|
C | CTTCT | 12 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0125others(9): Show | 12 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.451-3337_451-3334d others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036665 | |||||
| chr10:113036665
|
C | CTTCTTTC others(1): Show |
14 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0078others(11): Show | 14 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-3341_451-3334d others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036665 | |||||
| chr10:113036665
|
C | CTTCTTTC others(5): Show |
26 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.451-3345_451-3334d others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036665 | |||||
| chr10:113036665
|
C | CTTCTTTC others(13): Show |
1 | a0001c0001t0046g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.451-3353_451-3334d others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036665 | |||||
| chr10:113036665
|
CTTCTTTC others(1): Show |
C | 3 | a0001c0001t0002g0094a0001c0001t0007g0032a0001c0001t0016g0023 | 3 | HG02165.hp1 HG02165.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.451-3341_451-3334d others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 113036665 | |||||
| chr10:113036749
|
A | G | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-3276A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036749 | ||||||
| chr10:113036823
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451-3202G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036823 | ||||||
| chr10:113036906
|
A | G | 1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.451-3119A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036906 | ||||||
| chr10:113036923
|
G | A | 1 | a0002c0002t0007g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.451-3102G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113036923 | ||||||
| chr10:113037205
|
A | G | 2 | a0001c0001t0005g0033a0004c0006t0001g0039 | 2 | HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.451-2820A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037205 | ||||||
| chr10:113037292
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0196a0001c0001t0018g0069 | 3 | HG02132.hp2 HG03831.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.451-2733G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037292 | ||||||
| chr10:113037571
|
A | T | 1 | a0001c0001t0002g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.451-2454A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037571 | ||||||
| chr10:113037595
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0028g0014 | 2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.451-2430T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037595 | ||||||
| chr10:113037608
|
T | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.451-2417T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037608 | ||||||
| chr10:113037681
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-2344C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037681 | ||||||
| chr10:113037712
|
C | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0194a0001c0001t0002g0118others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-2313C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037712 | ||||||
| chr10:113037741
|
G | A | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-2284G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037741 | ||||||
| chr10:113037850
|
G | A | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.451-2175G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113037850 | ||||||
| chr10:113038030
|
T | C | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.451-1995T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038030 | ||||||
| chr10:113038134
|
G | A | 53 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.451-1891G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038134 | ||||||
| chr10:113038207
|
C | T | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-1818C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038207 | ||||||
| chr10:113038217
|
C | T | 2 | a0001c0001t0001g0087a0005c0010t0003g0167 | 2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.451-1808C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038217 | ||||||
| chr10:113038288
|
G | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.451-1737G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038288 | ||||||
| chr10:113038541
|
C | G | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451-1484C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038541 | ||||||
| chr10:113038612
|
C | T | 1 | a0001c0001t0038g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.451-1413C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038612 | ||||||
| chr10:113038627
|
C | G | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.451-1398C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113038627 | ||||||
| chr10:113039106
|
T | A | 1 | a0001c0004t0008g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451-919T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039106 | ||||||
| chr10:113039134
|
T | A | 46 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(43): Show | 46 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.451-891T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039134 | ||||||
| chr10:113039135
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.451-890T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039135 | ||||||
| chr10:113039246
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-779G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039246 | ||||||
| chr10:113039257
|
G | C | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.451-768G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039257 | ||||||
| chr10:113039332
|
G | A | 10 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-693G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039332 | ||||||
| chr10:113039397
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0195 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.451-628T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039397 | ||||||
| chr10:113039413
|
A | G | 35 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(32): Show | 35 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.451-612A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039413 | ||||||
| chr10:113039552
|
C | T | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-473C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039552 | ||||||
| chr10:113039709
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.451-316C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039709 | ||||||
| chr10:113039887
|
T | A | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-138T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 4/14 | chr10 | 113039887 | ||||||
| chr10:113040681
|
C | CT | 3 | a0001c0001t0002g0173a0001c0001t0041g0180a0002c0002t0003g0171 | 3 | HG01978.hp2 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.552+558dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113040681 | |||||
| chr10:113041287
|
C | T | 1 | a0001c0001t0006g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.552+1161C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113041287 | ||||||
| chr10:113041680
|
T | C | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+1554T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113041680 | ||||||
| chr10:113041728
|
T | A | 1 | a0001c0001t0002g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.552+1602T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113041728 | ||||||
| chr10:113041729
|
A | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 19 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.552+1603A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113041729 | ||||||
| chr10:113041766
|
G | A | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.552+1640G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113041766 | ||||||
| chr10:113041905
|
A | G | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+1779A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113041905 | ||||||
| chr10:113042043
|
G | T | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+1917G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042043 | ||||||
| chr10:113042179
|
C | G | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.552+2053C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042179 | ||||||
| chr10:113042249
|
C | A | 2 | a0001c0001t0005g0033a0004c0006t0001g0039 | 2 | HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.552+2123C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042249 | ||||||
| chr10:113042302
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.552+2176C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042302 | ||||||
| chr10:113042431
|
G | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+2305G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042431 | ||||||
| chr10:113042476
|
A | G | 1 | a0002c0002t0003g0171 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.552+2350A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042476 | ||||||
| chr10:113042524
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0008g0148 | 3 | HG02572.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.552+2398T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042524 | ||||||
| chr10:113042538
|
G | A | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+2412G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042538 | ||||||
| chr10:113042679
|
G | A | 1 | a0001c0001t0009g0073 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.552+2553G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113042679 | ||||||
| chr10:113043146
|
A | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.552+3020A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043146 | ||||||
| chr10:113043286
|
T | G | 5 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0011g0175others(2): Show | 5 | HG01081.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+3160T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043286 | ||||||
| chr10:113043306
|
G | C | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.552+3180G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043306 | ||||||
| chr10:113043338
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.552+3212T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043338 | ||||||
| chr10:113043439
|
A | G | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+3313A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043439 | ||||||
| chr10:113043534
|
A | G | 9 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+3408A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043534 | ||||||
| chr10:113043548
|
A | T | 13 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.552+3422A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043548 | ||||||
| chr10:113043806
|
A | G | 2 | a0001c0001t0006g0005a0007c0008t0002g0015 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.552+3680A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043806 | ||||||
| chr10:113043875
|
G | A | 2 | a0001c0001t0014g0153a0003c0003t0020g0135 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.552+3749G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113043875 | ||||||
| chr10:113044003
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.552+3877G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044003 | ||||||
| chr10:113044040
|
G | A | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.552+3914G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044040 | ||||||
| chr10:113044383
|
A | G | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.552+4257A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044383 | ||||||
| chr10:113044467
|
G | T | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.552+4341G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044467 | ||||||
| chr10:113044587
|
G | T | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+4461G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044587 | ||||||
| chr10:113044589
|
G | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(6): Show | 9 | HG01258.hp1 HG01981.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+4463G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044589 | ||||||
| chr10:113044613
|
A | T | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+4487A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044613 | ||||||
| chr10:113044676
|
A | G | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+4550A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044676 | ||||||
| chr10:113044833
|
C | T | 6 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+4707C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044833 | ||||||
| chr10:113044864
|
G | A | 2 | a0001c0001t0011g0175a0001c0001t0011g0184 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.552+4738G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044864 | ||||||
| chr10:113044867
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0028g0014 | 2 | HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.552+4741G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044867 | ||||||
| chr10:113044895
|
G | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.552+4769G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113044895 | ||||||
| chr10:113045032
|
G | A | 1 | a0004c0006t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.552+4906G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045032 | ||||||
| chr10:113045034
|
G | A | 9 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+4908G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045034 | ||||||
| chr10:113045037
|
A | C | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+4911A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045037 | ||||||
| chr10:113045089
|
C | T | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+4963C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045089 | ||||||
| chr10:113045134
|
C | G | 1 | a0002c0002t0018g0022 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.552+5008C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045134 | ||||||
| chr10:113045196
|
C | G | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.552+5070C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045196 | ||||||
| chr10:113045197
|
C | T | 4 | a0001c0001t0004g0097a0001c0001t0013g0103a0001c0001t0024g0121others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+5071C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045197 | ||||||
| chr10:113045346
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+5220C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045346 | ||||||
| chr10:113045421
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0013g0151 | 3 | HG02109.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.552+5295G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045421 | ||||||
| chr10:113045661
|
C | T | 9 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+5535C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045661 | ||||||
| chr10:113045673
|
G | A | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.552+5547G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045673 | ||||||
| chr10:113045840
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.552+5714G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045840 | ||||||
| chr10:113045841
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.552+5715C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045841 | ||||||
| chr10:113045993
|
A | G | 6 | a0001c0001t0001g0068a0001c0001t0004g0075a0001c0001t0006g0013others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.552+5867A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113045993 | ||||||
| chr10:113046073
|
G | A | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+5947G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046073 | ||||||
| chr10:113046101
|
C | A | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.552+5975C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046101 | ||||||
| chr10:113046109
|
C | G | 1 | a0001c0001t0002g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.552+5983C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046109 | ||||||
| chr10:113046353
|
A | G | 1 | a0001c0001t0014g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.552+6227A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046353 | ||||||
| chr10:113046457
|
A | G | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+6331A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046457 | ||||||
| chr10:113046655
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.552+6529A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046655 | ||||||
| chr10:113046666
|
G | A | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+6540G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046666 | ||||||
| chr10:113046674
|
TA | T | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+6550delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113046674 | |||||
| chr10:113046681
|
G | T | 3 | a0001c0004t0008g0144a0001c0004t0008g0146a0001c0004t0013g0147 | 3 | HG01109.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.552+6555G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046681 | ||||||
| chr10:113046797
|
C | T | 1 | a0001c0001t0013g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.552+6671C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046797 | ||||||
| chr10:113046867
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.552+6741C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046867 | ||||||
| chr10:113046908
|
G | A | 1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.552+6782G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046908 | ||||||
| chr10:113046938
|
G | A | 22 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(19): Show | 22 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.552+6812G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113046938 | ||||||
| chr10:113047229
|
A | C | 2 | a0001c0001t0004g0075a0001c0001t0006g0013 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.552+7103A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047229 | ||||||
| chr10:113047272
|
C | G | 9 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0075others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+7146C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047272 | ||||||
| chr10:113047288
|
G | C | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.552+7162G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047288 | ||||||
| chr10:113047356
|
C | T | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+7230C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047356 | ||||||
| chr10:113047398
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.552+7272C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047398 | ||||||
| chr10:113047399
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0003g0182 | 2 | HG00735.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.552+7273G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047399 | ||||||
| chr10:113047462
|
G | T | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+7336G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047462 | ||||||
| chr10:113047908
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.552+7782C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047908 | ||||||
| chr10:113047918
|
G | A | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+7792G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113047918 | ||||||
| chr10:113048019
|
G | A | 1 | a0001c0001t0008g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.552+7893G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048019 | ||||||
| chr10:113048078
|
G | A | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098 | 3 | HG03130.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552+7952G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048078 | ||||||
| chr10:113048313
|
T | C | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.552+8187T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048313 | ||||||
| chr10:113048338
|
A | G | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+8212A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048338 | ||||||
| chr10:113048424
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.552+8298A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048424 | ||||||
| chr10:113048669
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.552+8543G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048669 | ||||||
| chr10:113048669
|
G | T | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+8543G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048669 | ||||||
| chr10:113048730
|
AGGC | A | 3 | a0001c0001t0005g0065a0001c0001t0009g0081a0001c0001t0034g0187 | 3 | HG00099.hp2 HG01106.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.552+8605_552+8607d others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048730 | ||||||
| chr10:113048768
|
G | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+8642G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048768 | ||||||
| chr10:113048940
|
G | C | 1 | a0001c0001t0042g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.552+8814G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113048940 | ||||||
| chr10:113049076
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+8950G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049076 | ||||||
| chr10:113049143
|
G | T | 51 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(48): Show | 51 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.552+9017G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049143 | ||||||
| chr10:113049348
|
C | T | 1 | a0002c0002t0005g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.552+9222C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049348 | ||||||
| chr10:113049390
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0005g0122 | 2 | HG01123.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.552+9264C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049390 | ||||||
| chr10:113049459
|
C | T | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+9333C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049459 | ||||||
| chr10:113049475
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.552+9349C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049475 | ||||||
| chr10:113049531
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.552+9405C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049531 | ||||||
| chr10:113049532
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.552+9406C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049532 | ||||||
| chr10:113049560
|
G | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+9434G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049560 | ||||||
| chr10:113049609
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.552+9483A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049609 | ||||||
| chr10:113049636
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.552+9510C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049636 | ||||||
| chr10:113049692
|
T | A | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+9566T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049692 | ||||||
| chr10:113049702
|
C | T | 2 | a0001c0001t0004g0016a0001c0001t0004g0133 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+9576C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049702 | ||||||
| chr10:113049812
|
A | T | 1 | a0001c0001t0009g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.552+9686A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049812 | ||||||
| chr10:113049850
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.552+9724C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049850 | ||||||
| chr10:113049917
|
G | T | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+9791G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049917 | ||||||
| chr10:113049948
|
G | A | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+9822G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113049948 | ||||||
| chr10:113050077
|
G | A | 8 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(5): Show | 8 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+9951G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113050077 | ||||||
| chr10:113050188
|
A | G | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+10062A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113050188 | ||||||
| chr10:113050391
|
G | C | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+10265G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113050391 | ||||||
| chr10:113050481
|
T | C | 114 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.552+10355T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113050481 | ||||||
| chr10:113050505
|
C | T | 5 | a0001c0001t0001g0123a0001c0001t0009g0080a0001c0001t0030g0004others(2): Show | 5 | HG02965.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+10379C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113050505 | ||||||
| chr10:113050761
|
C | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0190a0001c0001t0001g0193 | 3 | HG02735.hp2 NA18950.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.552+10635C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113050761 | ||||||
| chr10:113051025
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.552+10899C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051025 | ||||||
| chr10:113051072
|
T | C | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+10946T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051072 | ||||||
| chr10:113051203
|
C | CCA | 63 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.552+11116_552+1111 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
C | CCACA | 24 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0063others(21): Show | 24 | HG00140.hp1 HG00408.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.552+11114_552+1111 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
C | CCACACA | 15 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0079others(12): Show | 15 | HG00408.hp1 HG02647.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.552+11112_552+1111 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
C | CCACACAC others(1): Show |
5 | a0001c0001t0001g0125a0001c0001t0002g0107a0001c0001t0002g0118others(2): Show | 5 | HG00099.hp1 HG00642.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+11110_552+1111 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
C | CCACACAC others(3): Show |
3 | a0001c0001t0004g0126a0001c0001t0010g0127a0001c0001t0026g0124 | 3 | HG02145.hp2 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.552+11108_552+1111 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
C | CCACACAC others(7): Show |
2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+11104_552+1111 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
CCA | C | 6 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0006g0149others(3): Show | 6 | HG02970.hp2 HG03130.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.552+11116_552+1111 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
CCACA | C | 3 | a0001c0001t0005g0065a0001c0001t0009g0081a0001c0001t0045g0156 | 3 | HG00099.hp2 HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.552+11114_552+1111 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
CCACACAC others(1): Show |
C | 5 | a0001c0001t0001g0101a0001c0001t0002g0142a0001c0004t0008g0144others(2): Show | 5 | HG01109.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+11110_552+1111 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
CCACACAC others(3): Show |
C | 4 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0008g0139others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+11108_552+1111 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
CCACACAC others(5): Show |
C | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.552+11106_552+1111 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051203
|
CCACACAC others(13): Show |
C | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.552+11098_552+1111 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051203 | |||||
| chr10:113051238
|
CACACAG | C | 2 | a0001c0001t0001g0017a0002c0002t0003g0162 | 2 | NA19070.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.552+11118_552+1112 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051238 | |||||
| chr10:113051240
|
CACAG | C | 16 | a0001c0001t0001g0018a0001c0001t0001g0040a0001c0001t0001g0086others(13): Show | 16 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.552+11118_552+1112 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051240 | |||||
| chr10:113051242
|
CAG | C | 8 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0123others(5): Show | 8 | HG00735.hp1 HG01943.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+11118_552+1111 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051242 | |||||
| chr10:113051242
|
CAGACACA others(1): Show |
C | 3 | a0001c0001t0011g0175a0001c0001t0011g0184a0001c0001t0014g0055 | 3 | HG01081.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.552+11118_552+1112 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051242 | |||||
| chr10:113051244
|
G | C | 11 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0002g0094others(8): Show | 11 | HG00597.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.552+11118G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051244 | ||||||
| chr10:113051244
|
G | T | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.552+11118G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051244 | ||||||
| chr10:113051250
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(24): Show | 27 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.552+11124T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051250 | ||||||
| chr10:113051268
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.552+11142G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051268 | ||||||
| chr10:113051539
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.552+11413C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051539 | ||||||
| chr10:113051557
|
T | C | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.552+11431T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113051557 | ||||||
| chr10:113051994
|
CACTT | C | 2 | a0001c0001t0001g0131a0001c0001t0002g0006 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.552+11873_552+1187 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113051994 | |||||
| chr10:113052060
|
C | T | 1 | a0002c0002t0018g0022 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.552+11934C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052060 | ||||||
| chr10:113052082
|
T | C | 1 | a0001c0001t0012g0178 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.552+11956T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052082 | ||||||
| chr10:113052312
|
T | C | 101 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(98): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.552+12186T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052312 | ||||||
| chr10:113052444
|
A | G | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+12318A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052444 | ||||||
| chr10:113052564
|
A | G | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.552+12438A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052564 | ||||||
| chr10:113052631
|
T | C | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+12505T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052631 | ||||||
| chr10:113052861
|
A | G | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+12735A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052861 | ||||||
| chr10:113052879
|
T | A | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+12753T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052879 | ||||||
| chr10:113052968
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.552+12842G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113052968 | ||||||
| chr10:113053020
|
T | C | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+12894T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053020 | ||||||
| chr10:113053085
|
G | A | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.552+12959G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053085 | ||||||
| chr10:113053123
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.552+12997G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053123 | ||||||
| chr10:113053201
|
A | G | 4 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | HG00642.hp2 HG01243.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+13075A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053201 | ||||||
| chr10:113053282
|
C | T | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.552+13156C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053282 | ||||||
| chr10:113053288
|
C | T | 106 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.552+13162C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053288 | ||||||
| chr10:113053368
|
G | A | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.552+13242G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053368 | ||||||
| chr10:113053516
|
A | G | 2 | a0001c0001t0005g0033a0004c0006t0001g0039 | 2 | HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.552+13390A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053516 | ||||||
| chr10:113053662
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.552+13536C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113053662 | ||||||
| chr10:113053989
|
C | CACAT | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+13867_552+1387 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113053989 | |||||
| chr10:113054000
|
G | A | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+13874G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054000 | ||||||
| chr10:113054035
|
G | C | 1 | a0001c0001t0005g0033 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.552+13909G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054035 | ||||||
| chr10:113054212
|
T | C | 199 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.552+14086T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054212 | ||||||
| chr10:113054439
|
A | G | 6 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(3): Show | 6 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+14313A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054439 | ||||||
| chr10:113054693
|
A | G | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+14567A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054693 | ||||||
| chr10:113054728
|
T | A | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+14602T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054728 | ||||||
| chr10:113054731
|
T | A | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+14605T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054731 | ||||||
| chr10:113054766
|
T | C | 7 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+14640T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054766 | ||||||
| chr10:113054904
|
A | T | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+14778A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113054904 | ||||||
| chr10:113055038
|
T | G | 6 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+14912T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113055038 | ||||||
| chr10:113055128
|
A | G | 6 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+15002A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113055128 | ||||||
| chr10:113055207
|
C | A | 7 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+15081C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113055207 | ||||||
| chr10:113055329
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.552+15203C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113055329 | ||||||
| chr10:113055707
|
T | G | 10 | a0001c0001t0002g0102a0001c0001t0002g0117a0001c0001t0003g0186others(7): Show | 10 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+15581T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113055707 | ||||||
| chr10:113055854
|
A | C | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.552+15728A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113055854 | ||||||
| chr10:113056011
|
C | G | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.552+15885C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113056011 | ||||||
| chr10:113056165
|
A | G | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.552+16039A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113056165 | ||||||
| chr10:113056313
|
C | T | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+16187C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113056313 | ||||||
| chr10:113056507
|
GT | G | 8 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+16383delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113056507 | |||||
| chr10:113056571
|
T | C | 1 | a0002c0002t0001g0028 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.552+16445T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113056571 | ||||||
| chr10:113056746
|
G | C | 7 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0008g0139others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+16620G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113056746 | ||||||
| chr10:113056917
|
C | G | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+16791C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113056917 | ||||||
| chr10:113057039
|
T | C | 8 | a0001c0001t0001g0130a0001c0001t0002g0142a0001c0001t0004g0134others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+16913T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057039 | ||||||
| chr10:113057198
|
T | C | 2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.552+17072T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057198 | ||||||
| chr10:113057250
|
A | C | 36 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(33): Show | 36 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.552+17124A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057250 | ||||||
| chr10:113057391
|
G | A | 1 | a0002c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.552+17265G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057391 | ||||||
| chr10:113057430
|
C | T | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+17304C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057430 | ||||||
| chr10:113057477
|
A | G | 10 | a0001c0001t0001g0062a0001c0001t0001g0068a0001c0001t0004g0075others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+17351A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057477 | ||||||
| chr10:113057530
|
G | A | 2 | a0001c0001t0005g0033a0004c0006t0001g0039 | 2 | HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.552+17404G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057530 | ||||||
| chr10:113057768
|
T | C | 3 | a0001c0001t0002g0095a0001c0001t0004g0016a0001c0001t0004g0133 | 3 | HG01884.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.552+17642T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057768 | ||||||
| chr10:113057768
|
T | G | 110 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.552+17642T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057768 | ||||||
| chr10:113057901
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.552+17775G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113057901 | ||||||
| chr10:113058044
|
G | C | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+17918G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058044 | ||||||
| chr10:113058066
|
C | T | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.552+17940C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058066 | ||||||
| chr10:113058112
|
G | A | 2 | a0001c0001t0005g0033a0004c0006t0001g0039 | 2 | HG02257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.552+17986G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058112 | ||||||
| chr10:113058186
|
C | T | 2 | a0001c0001t0005g0064a0002c0002t0001g0192 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+18060C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058186 | ||||||
| chr10:113058283
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0008g0148 | 3 | HG02572.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.552+18157C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058283 | ||||||
| chr10:113058387
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.552+18261C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058387 | ||||||
| chr10:113058402
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+18276C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058402 | ||||||
| chr10:113058517
|
C | G | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+18391C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058517 | ||||||
| chr10:113058556
|
C | T | 1 | a0001c0001t0044g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.552+18430C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058556 | ||||||
| chr10:113058694
|
C | CTG | 7 | a0001c0001t0004g0132a0001c0001t0005g0054a0001c0001t0006g0136others(4): Show | 7 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+18583_552+1858 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113058694 | |||||
| chr10:113058711
|
C | T | 2 | a0001c0001t0012g0165a0002c0002t0005g0043 | 2 | HG01081.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.552+18585C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058711 | ||||||
| chr10:113058722
|
G | A | 4 | a0001c0001t0001g0086a0001c0001t0003g0172a0001c0001t0005g0199others(1): Show | 4 | HG01981.hp2 HG02738.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+18596G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058722 | ||||||
| chr10:113058725
|
G | A | 1 | a0001c0001t0005g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.552+18599G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058725 | ||||||
| chr10:113058995
|
G | A | 70 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0041others(67): Show | 70 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.552+18869G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113058995 | ||||||
| chr10:113059008
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.552+18882C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113059008 | ||||||
| chr10:113059013
|
G | A | 111 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0031others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.552+18887G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113059013 | ||||||
| chr10:113059318
|
G | T | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+19192G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113059318 | ||||||
| chr10:113059369
|
A | C | 3 | a0001c0001t0006g0149a0001c0001t0008g0092a0001c0001t0008g0093 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.552+19243A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113059369 | ||||||
| chr10:113059427
|
A | G | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+19301A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113059427 | ||||||
| chr10:113059906
|
G | T | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.552+19780G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113059906 | ||||||
| chr10:113060090
|
A | G | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+19964A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113060090 | ||||||
| chr10:113060432
|
T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(12): Show | 15 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.552+20306T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113060432 | ||||||
| chr10:113060593
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.552+20467C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113060593 | ||||||
| chr10:113060636
|
A | G | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+20510A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113060636 | ||||||
| chr10:113060657
|
C | T | 3 | a0001c0001t0006g0149a0001c0001t0008g0092a0001c0001t0008g0093 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.552+20531C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113060657 | ||||||
| chr10:113060745
|
G | A | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.552+20619G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113060745 | ||||||
| chr10:113061036
|
A | C | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+20910A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061036 | ||||||
| chr10:113061098
|
T | G | 1 | a0001c0004t0008g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.552+20972T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061098 | ||||||
| chr10:113061202
|
G | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.552+21076G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061202 | ||||||
| chr10:113061210
|
A | T | 1 | a0001c0001t0013g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.552+21084A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061210 | ||||||
| chr10:113061217
|
G | A | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.552+21091G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061217 | ||||||
| chr10:113061324
|
A | G | 3 | a0001c0001t0001g0130a0001c0001t0004g0134a0001c0001t0013g0151 | 3 | HG02109.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.552+21198A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061324 | ||||||
| chr10:113061341
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0028g0014a0004c0006t0001g0039 | 3 | HG02257.hp2 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.552+21215C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061341 | ||||||
| chr10:113061490
|
T | C | 108 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.552+21364T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061490 | ||||||
| chr10:113061655
|
G | A | 1 | a0003c0003t0032g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.552+21529G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061655 | ||||||
| chr10:113061740
|
C | T | 1 | a0001c0001t0011g0176 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.552+21614C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061740 | ||||||
| chr10:113061768
|
A | G | 15 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 15 | HG00642.hp2 HG00738.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.552+21642A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061768 | ||||||
| chr10:113061795
|
C | T | 81 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(78): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.552+21669C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061795 | ||||||
| chr10:113061831
|
A | G | 1 | a0002c0002t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.552+21705A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061831 | ||||||
| chr10:113061832
|
C | T | 7 | a0001c0001t0001g0068a0001c0001t0004g0075a0001c0001t0006g0013others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+21706C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113061832 | ||||||
| chr10:113062048
|
T | G | 104 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0040others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.552+21922T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062048 | ||||||
| chr10:113062190
|
C | T | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.552+22064C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062190 | ||||||
| chr10:113062385
|
C | T | 3 | a0001c0001t0006g0149a0001c0001t0008g0092a0001c0001t0008g0093 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.552+22259C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062385 | ||||||
| chr10:113062396
|
A | G | 1 | a0001c0001t0011g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.552+22270A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062396 | ||||||
| chr10:113062406
|
A | G | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.552+22280A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062406 | ||||||
| chr10:113062476
|
G | A | 1 | a0004c0006t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.552+22350G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062476 | ||||||
| chr10:113062540
|
C | T | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+22414C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062540 | ||||||
| chr10:113062704
|
C | T | 8 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0125others(5): Show | 8 | HG02145.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+22578C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062704 | ||||||
| chr10:113062842
|
T | C | 2 | a0001c0001t0005g0033a0001c0001t0005g0064 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+22716T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062842 | ||||||
| chr10:113062888
|
G | GT | 3 | a0001c0001t0005g0033a0001c0001t0005g0064a0002c0002t0001g0200 | 3 | HG00597.hp1 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+22766dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113062888 | |||||
| chr10:113062939
|
T | C | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.552+22813T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062939 | ||||||
| chr10:113062976
|
G | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(23): Show | 26 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.552+22850G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062976 | ||||||
| chr10:113062979
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.552+22853C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062979 | ||||||
| chr10:113062980
|
A | G | 104 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.552+22854A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113062980 | ||||||
| chr10:113063003
|
G | A | 1 | a0001c0001t0007g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552+22877G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113063003 | ||||||
| chr10:113063204
|
T | C | 3 | a0001c0001t0006g0149a0001c0001t0008g0092a0001c0001t0008g0093 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.552+23078T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113063204 | ||||||
| chr10:113063322
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0101 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.552+23196C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113063322 | ||||||
| chr10:113063603
|
C | T | 10 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0190others(7): Show | 10 | HG00438.hp1 HG01978.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.552+23477C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113063603 | ||||||
| chr10:113063667
|
A | G | 107 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.552+23541A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113063667 | ||||||
| chr10:113063722
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.552+23596G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113063722 | ||||||
| chr10:113063797
|
T | C | 3 | a0001c0001t0011g0159a0001c0001t0037g0160a0001c0004t0013g0145 | 3 | HG02572.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+23671T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113063797 | ||||||
| chr10:113063893
|
C | CGT | 63 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0038others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.552+23796_552+2379 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113063893 | |||||
| chr10:113063893
|
C | CGTGT | 60 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.552+23794_552+2379 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113063893 | |||||
| chr10:113063893
|
C | CGTGTGT | 17 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0056others(14): Show | 17 | HG00642.hp2 HG00738.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.552+23792_552+2379 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113063893 | |||||
| chr10:113063893
|
C | CGTGTGTG others(1): Show |
13 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0004g0075others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.552+23790_552+2379 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113063893 | |||||
| chr10:113063893
|
CGT | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0061others(24): Show | 27 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.552+23796_552+2379 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113063893 | |||||
| chr10:113063893
|
CGTGT | C | 9 | a0001c0001t0002g0104a0001c0001t0002g0113a0001c0001t0002g0115others(6): Show | 9 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+23794_552+2379 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113063893 | |||||
| chr10:113064015
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.552+23889G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064015 | ||||||
| chr10:113064071
|
C | T | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098 | 3 | HG03130.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552+23945C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064071 | ||||||
| chr10:113064177
|
C | G | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.552+24051C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064177 | ||||||
| chr10:113064289
|
G | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0064 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+24163G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064289 | ||||||
| chr10:113064465
|
T | G | 105 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0038others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.552+24339T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064465 | ||||||
| chr10:113064597
|
C | A | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.552+24471C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064597 | ||||||
| chr10:113064649
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.552+24523G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064649 | ||||||
| chr10:113064714
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0047others(34): Show | 37 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.552+24588G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064714 | ||||||
| chr10:113064744
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+24618C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064744 | ||||||
| chr10:113064905
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.552+24779G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064905 | ||||||
| chr10:113064997
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.552+24871C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113064997 | ||||||
| chr10:113065028
|
GT | G | 5 | a0001c0001t0006g0149a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02895.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+24903delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065028 | ||||||
| chr10:113065051
|
G | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0130a0001c0001t0004g0134 | 3 | HG02109.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.552+24925G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065051 | ||||||
| chr10:113065217
|
C | T | 150 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.552+25091C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065217 | ||||||
| chr10:113065252
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.552+25126T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065252 | ||||||
| chr10:113065397
|
A | G | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0010g0098 | 3 | HG03130.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552+25271A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065397 | ||||||
| chr10:113065588
|
G | A | 1 | a0001c0001t0010g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.552+25462G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065588 | ||||||
| chr10:113065901
|
C | T | 7 | a0001c0001t0001g0062a0001c0001t0005g0033a0001c0001t0005g0064others(4): Show | 7 | HG00597.hp1 HG02559.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+25775C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065901 | ||||||
| chr10:113065964
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.552+25838G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113065964 | ||||||
| chr10:113066054
|
A | G | 27 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0036others(24): Show | 27 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.552+25928A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066054 | ||||||
| chr10:113066070
|
G | T | 1 | a0001c0001t0011g0175 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.552+25944G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066070 | ||||||
| chr10:113066330
|
A | T | 5 | a0001c0001t0001g0074a0001c0001t0004g0133a0001c0001t0009g0080others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+26204A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066330 | ||||||
| chr10:113066360
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+26234C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066360 | ||||||
| chr10:113066365
|
C | CA | 7 | a0001c0001t0001g0062a0001c0001t0005g0033a0001c0001t0005g0064others(4): Show | 7 | HG00597.hp1 HG02559.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+26253dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113066365 | |||||
| chr10:113066401
|
C | T | 11 | a0001c0001t0001g0101a0001c0001t0001g0130a0001c0001t0002g0012others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.552+26275C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066401 | ||||||
| chr10:113066543
|
A | T | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+26417A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066543 | ||||||
| chr10:113066550
|
G | C | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+26424G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066550 | ||||||
| chr10:113066731
|
C | T | 3 | a0001c0001t0001g0031a0001c0001t0002g0096a0001c0001t0022g0050 | 3 | HG01255.hp2 HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.552+26605C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066731 | ||||||
| chr10:113066943
|
G | T | 1 | a0001c0001t0013g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.552+26817G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066943 | ||||||
| chr10:113066979
|
G | T | 3 | a0001c0001t0001g0031a0001c0001t0002g0096a0001c0001t0022g0050 | 3 | HG01255.hp2 HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.552+26853G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113066979 | ||||||
| chr10:113067425
|
T | A | 12 | a0001c0001t0001g0101a0001c0001t0001g0130a0001c0001t0002g0012others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.552+27299T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113067425 | ||||||
| chr10:113067546
|
G | GTGAA | 2 | a0001c0001t0005g0033a0001c0001t0005g0064 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+27422_552+2742 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113067546 | |||||
| chr10:113067586
|
C | G | 1 | a0001c0001t0006g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.552+27460C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113067586 | ||||||
| chr10:113067602
|
G | A | 1 | a0001c0001t0006g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.552+27476G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113067602 | ||||||
| chr10:113067852
|
G | GTTTTGTT others(7): Show |
199 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.552+27727_552+2774 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113067852 | |||||
| chr10:113067941
|
C | A | 2 | a0001c0001t0005g0033a0001c0001t0005g0064 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+27815C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113067941 | ||||||
| chr10:113068289
|
C | T | 3 | a0001c0001t0010g0127a0001c0005t0019g0001a0001c0005t0019g0002 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.552+28163C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068289 | ||||||
| chr10:113068406
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.552+28280G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068406 | ||||||
| chr10:113068432
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.552+28306G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068432 | ||||||
| chr10:113068467
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0004g0076others(2): Show | 5 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+28341G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068467 | ||||||
| chr10:113068523
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0064 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+28397A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068523 | ||||||
| chr10:113068562
|
C | T | 2 | a0001c0001t0001g0123a0003c0003t0011g0009 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.552+28436C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068562 | ||||||
| chr10:113068645
|
A | G | 7 | a0001c0001t0001g0062a0001c0001t0005g0033a0001c0001t0005g0064others(4): Show | 7 | HG00597.hp1 HG02559.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+28519A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068645 | ||||||
| chr10:113068835
|
T | C | 11 | a0001c0001t0001g0101a0001c0001t0001g0130a0001c0001t0002g0012others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.552+28709T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068835 | ||||||
| chr10:113068896
|
A | G | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.552+28770A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068896 | ||||||
| chr10:113068899
|
CT | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0078others(6): Show | 9 | HG00735.hp2 HG01099.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.552+28786delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113068899 | |||||
| chr10:113068901
|
T | C | 2 | a0001c0001t0005g0033a0001c0001t0005g0064 | 2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+28775T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068901 | ||||||
| chr10:113068921
|
A | G | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.552+28795A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068921 | ||||||
| chr10:113068959
|
C | T | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+28833C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113068959 | ||||||
| chr10:113069038
|
T | G | 2 | a0001c0001t0037g0160a0001c0004t0013g0145 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.552+28912T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069038 | ||||||
| chr10:113069233
|
C | CT | 15 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0130others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.552+29122dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113069233 | |||||
| chr10:113069386
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.552+29260C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069386 | ||||||
| chr10:113069420
|
G | C | 3 | a0001c0001t0005g0033a0001c0001t0005g0064a0002c0002t0001g0200 | 3 | HG00597.hp1 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+29294G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069420 | ||||||
| chr10:113069519
|
C | T | 2 | a0001c0001t0016g0023a0001c0001t0039g0166 | 2 | HG02165.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.552+29393C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069519 | ||||||
| chr10:113069674
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.552+29548C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069674 | ||||||
| chr10:113069856
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.552+29730C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069856 | ||||||
| chr10:113069892
|
G | A | 1 | a0001c0013t0027g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.552+29766G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069892 | ||||||
| chr10:113069936
|
T | C | 149 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(146): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.552+29810T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113069936 | ||||||
| chr10:113070009
|
G | T | 1 | a0001c0001t0009g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.552+29883G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070009 | ||||||
| chr10:113070010
|
C | T | 158 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.552+29884C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070010 | ||||||
| chr10:113070120
|
G | C | 5 | a0001c0001t0006g0149a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02895.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+29994G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070120 | ||||||
| chr10:113070155
|
C | G | 1 | a0001c0001t0002g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.552+30029C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070155 | ||||||
| chr10:113070182
|
T | C | 199 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.552+30056T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070182 | ||||||
| chr10:113070187
|
C | T | 3 | a0001c0001t0005g0033a0001c0001t0005g0064a0002c0002t0001g0200 | 3 | HG00597.hp1 HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.552+30061C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070187 | ||||||
| chr10:113070204
|
C | T | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.552+30078C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070204 | ||||||
| chr10:113070233
|
C | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0002g0095others(1): Show | 4 | HG02258.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+30107C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070233 | ||||||
| chr10:113070254
|
TA | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0100others(7): Show | 10 | HG00642.hp2 HG00738.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.552+30141delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070254 | |||||
| chr10:113070265
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.552+30139A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070265 | ||||||
| chr10:113070266
|
A | AAATTTAT others(4): Show |
1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552+30141_552+3014 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070266 | |||||
| chr10:113070266
|
A | ATTT | 7 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0016g0024others(4): Show | 7 | HG02132.hp1 HG02132.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+30140_552+3014 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070266 | ||||||
| chr10:113070266
|
A | ATTTAT | 62 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0040others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.552+30140_552+3014 others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070266 | ||||||
| chr10:113070266
|
A | ATTTATAT | 8 | a0001c0001t0001g0044a0001c0001t0002g0102a0001c0001t0002g0117others(5): Show | 8 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+30140_552+3014 others(11): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070266 | ||||||
| chr10:113070266
|
A | ATTTATAT others(4): Show |
2 | a0001c0001t0001g0194a0009c0007t0001g0025 | 2 | HG02735.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.552+30140_552+3014 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070266 | ||||||
| chr10:113070266
|
A | ATTTATAT others(6): Show |
1 | a0001c0001t0013g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.552+30140_552+3014 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070266 | ||||||
| chr10:113070266
|
A | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0062a0001c0001t0002g0161others(1): Show | 4 | HG00323.hp2 HG02523.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+30140A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070266 | ||||||
| chr10:113070267
|
A | T | 4 | a0001c0001t0001g0129a0001c0001t0005g0033a0001c0001t0005g0064others(1): Show | 4 | HG02809.hp2 HG03942.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+30141A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070267 | ||||||
| chr10:113070269
|
T | A | 89 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.552+30143T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070269 | ||||||
| chr10:113070269
|
T | TA | 4 | a0001c0001t0001g0129a0001c0001t0005g0033a0001c0001t0005g0064others(1): Show | 4 | HG02809.hp2 HG03942.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+30143_552+3014 others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070269 | ||||||
| chr10:113070269
|
T | TTA | 11 | a0001c0001t0006g0136a0001c0001t0006g0149a0001c0001t0008g0092others(8): Show | 11 | HG01081.hp1 HG01109.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.552+30163_552+3016 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATA | 13 | a0001c0001t0001g0089a0001c0001t0001g0193a0001c0001t0002g0006others(10): Show | 13 | HG00099.hp1 HG00438.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.552+30161_552+3016 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATATA | 23 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0047others(20): Show | 23 | HG00597.hp2 HG01081.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.552+30159_552+3016 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATATAT others(1): Show |
17 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0086others(14): Show | 17 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.552+30157_552+3016 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0009g0080a0001c0001t0029g0114 | 2 | HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.552+30155_552+3016 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATATAT others(5): Show |
6 | a0001c0001t0001g0130a0001c0001t0004g0016a0001c0001t0004g0132others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.552+30153_552+3016 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATATAT others(7): Show |
2 | a0001c0001t0013g0151a0001c0001t0031g0010 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.552+30151_552+3016 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0001g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.552+30149_552+3016 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.552+30147_552+3016 others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
TTA | T | 2 | a0001c0001t0011g0176a0002c0002t0001g0200 | 2 | HG00597.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.552+30163_552+3016 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070269
|
TTATA | T | 4 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0004g0076others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+30161_552+3016 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070269 | |||||
| chr10:113070273
|
A | T | 3 | a0001c0001t0010g0127a0001c0005t0019g0001a0001c0005t0019g0002 | 3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.552+30147A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070273 | ||||||
| chr10:113070283
|
A | ATG | 10 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0058others(7): Show | 10 | HG00735.hp2 HG01099.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.552+30158_552+3015 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113070283 | |||||
| chr10:113070495
|
G | A | 182 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.552+30369G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070495 | ||||||
| chr10:113070547
|
G | A | 57 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0040others(54): Show | 57 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.552+30421G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070547 | ||||||
| chr10:113070613
|
A | G | 4 | a0001c0001t0001g0087a0001c0001t0007g0032a0002c0002t0001g0088others(1): Show | 4 | HG00597.hp2 HG02040.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+30487A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070613 | ||||||
| chr10:113070646
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0002g0096a0001c0001t0022g0050 | 3 | HG01255.hp2 HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.552+30520A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070646 | ||||||
| chr10:113070718
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.552+30592G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070718 | ||||||
| chr10:113070768
|
A | T | 1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.552+30642A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070768 | ||||||
| chr10:113070846
|
G | T | 3 | a0001c0001t0004g0132a0001c0001t0023g0027a0009c0007t0001g0025 | 3 | HG02622.hp2 HG03017.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.552+30720G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070846 | ||||||
| chr10:113070859
|
T | C | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.552+30733T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070859 | ||||||
| chr10:113070870
|
T | C | 1 | a0001c0001t0011g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.552+30744T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113070870 | ||||||
| chr10:113071045
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.552+30919C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071045 | ||||||
| chr10:113071166
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0004g0141others(1): Show | 4 | HG02486.hp1 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+31040C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071166 | ||||||
| chr10:113071273
|
G | A | 1 | a0001c0001t0043g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.552+31147G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071273 | ||||||
| chr10:113071293
|
T | G | 1 | a0002c0002t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.552+31167T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071293 | ||||||
| chr10:113071428
|
C | T | 2 | a0001c0001t0001g0193a0002c0002t0001g0090 | 2 | NA18950.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.552+31302C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071428 | ||||||
| chr10:113071675
|
A | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.552+31549A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071675 | ||||||
| chr10:113071700
|
G | A | 8 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(5): Show | 8 | HG01109.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+31574G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071700 | ||||||
| chr10:113071942
|
A | G | 1 | a0001c0001t0007g0020 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.552+31816A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113071942 | ||||||
| chr10:113072044
|
TTTAA | T | 39 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.552+31930_552+3193 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113072044 | |||||
| chr10:113072213
|
G | C | 2 | a0001c0001t0004g0126a0001c0001t0006g0157 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.552+32087G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072213 | ||||||
| chr10:113072243
|
G | A | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.552+32117G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072243 | ||||||
| chr10:113072396
|
C | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0193a0001c0001t0001g0196others(7): Show | 10 | HG00280.hp1 HG00735.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.552+32270C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072396 | ||||||
| chr10:113072545
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.552+32419G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072545 | ||||||
| chr10:113072597
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.552+32471G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072597 | ||||||
| chr10:113072713
|
T | C | 8 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+32587T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072713 | ||||||
| chr10:113072859
|
C | G | 1 | a0001c0001t0001g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.552+32733C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072859 | ||||||
| chr10:113072865
|
G | A | 1 | a0007c0008t0002g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.552+32739G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072865 | ||||||
| chr10:113072913
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0004g0016others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+32787C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113072913 | ||||||
| chr10:113073099
|
C | CGTGT | 3 | a0001c0001t0001g0131a0001c0001t0015g0008a0003c0003t0011g0009 | 3 | HG02630.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.552+33001_552+3300 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGT | 25 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(22): Show | 25 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.552+32999_552+3300 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGTG others(1): Show |
10 | a0001c0001t0001g0130a0001c0001t0002g0012a0001c0001t0004g0016others(7): Show | 10 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+32997_552+3300 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGTG others(3): Show |
19 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0129others(16): Show | 19 | HG01071.hp1 HG01099.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.552+32995_552+3300 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGTG others(5): Show |
15 | a0001c0001t0001g0068a0001c0001t0001g0099a0001c0001t0002g0094others(12): Show | 15 | HG00323.hp2 HG02559.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.552+32993_552+3300 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGTG others(7): Show |
2 | a0001c0001t0014g0055a0001c0001t0026g0124 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.552+32991_552+3300 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGTG others(9): Show |
3 | a0001c0001t0001g0079a0001c0001t0028g0014a0003c0003t0032g0011 | 3 | HG02717.hp2 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.552+32989_552+3300 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGTG others(11): Show |
1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.552+32987_552+3300 others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
C | CGTGTGTG others(13): Show |
2 | a0001c0001t0010g0098a0001c0001t0031g0010 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.552+32985_552+3300 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
CGT | C | 2 | a0001c0001t0002g0117a0001c0001t0007g0020 | 2 | HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.552+33003_552+3300 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073099
|
CGTGT | C | 54 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0036others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.552+33001_552+3300 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073099 | |||||
| chr10:113073100
|
G | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(13): Show |
intron_variant | MODIFIER | c.552+32974G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073100 | ||||||
| chr10:113073104
|
G | A | 1 | a0001c0001t0023g0027 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.552+32978G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073104 | ||||||
| chr10:113073127
|
T | A | 2 | a0001c0001t0002g0117a0001c0001t0007g0020 | 2 | HG01515.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.552+33001T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073127 | ||||||
| chr10:113073129
|
T | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0193a0001c0001t0001g0196others(7): Show | 10 | HG00280.hp1 HG00735.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.552+33003T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073129 | ||||||
| chr10:113073129
|
T | TGTGTGTG others(7): Show |
3 | a0001c0001t0004g0134a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.552+33004_552+3300 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(5): Show |
2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.552+33004_552+3300 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.552+33004_552+3300 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(5): Show |
2 | a0001c0001t0008g0092a0001c0001t0008g0093 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.552+33004_552+3300 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0016g0023 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.552+33004_552+3300 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(7): Show |
5 | a0001c0001t0001g0125a0001c0001t0002g0142a0001c0001t0004g0076others(2): Show | 5 | HG02647.hp1 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+33004_552+3300 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(9): Show |
20 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.552+33004_552+3300 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0040g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.552+33004_552+3300 others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(13): Show |
1 | a0002c0002t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.552+33004_552+3300 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(9): Show |
6 | a0001c0001t0001g0060a0001c0001t0006g0188a0001c0001t0010g0127others(3): Show | 6 | HG01243.hp2 HG01943.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+33004_552+3300 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(11): Show |
1 | a0002c0002t0010g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.552+33004_552+3300 others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0002g0155a0001c0001t0006g0013 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.552+33004_552+3300 others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(13): Show |
4 | a0001c0001t0001g0061a0001c0001t0001g0195a0001c0001t0002g0100others(1): Show | 4 | HG00438.hp1 HG01256.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+33004_552+3300 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073129
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0002g0128 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.552+33004_552+3300 others(26): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073129 | |||||
| chr10:113073131
|
A | T | 61 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0047others(58): Show | 61 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.552+33005A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073131 | ||||||
| chr10:113073133
|
A | T | 28 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0074others(25): Show | 28 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.552+33007A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073133 | ||||||
| chr10:113073251
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02257.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.552+33125C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073251 | ||||||
| chr10:113073308
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.552+33182A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073308 | ||||||
| chr10:113073503
|
C | CA | 20 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0056others(17): Show | 20 | HG00280.hp1 HG00735.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.552+33407dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073503 | |||||
| chr10:113073503
|
CA | C | 70 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0031others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.552+33407delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073503 | |||||
| chr10:113073503
|
CAA | C | 13 | a0001c0001t0001g0068a0001c0001t0001g0129a0001c0001t0001g0131others(10): Show | 13 | HG01081.hp2 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.552+33406_552+3340 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073503 | |||||
| chr10:113073503
|
CAAAA | C | 6 | a0001c0001t0006g0140a0001c0001t0006g0188a0001c0001t0010g0127others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.552+33404_552+3340 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073503 | |||||
| chr10:113073503
|
CAAAAA | C | 5 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(2): Show | 5 | HG02896.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+33403_552+3340 others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073503 | |||||
| chr10:113073503
|
CAAAAAAA others(3): Show |
C | 1 | a0007c0008t0002g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.552+33398_552+3340 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073503 | |||||
| chr10:113073503
|
CAAAAAAA others(4): Show |
C | 18 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0040others(15): Show | 18 | HG00597.hp2 HG01978.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.552+33397_552+3340 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073503 | |||||
| chr10:113073588
|
A | T | 3 | a0001c0001t0004g0134a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.552+33462A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073588 | ||||||
| chr10:113073644
|
A | G | 1 | a0001c0001t0017g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.552+33518A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073644 | ||||||
| chr10:113073693
|
G | GA | 6 | a0001c0001t0002g0012a0001c0001t0022g0050a0001c0001t0042g0177others(3): Show | 6 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+33580dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113073693 | |||||
| chr10:113073707
|
C | A | 2 | a0001c0001t0002g0142a0001c0001t0004g0076 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.552+33581C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073707 | ||||||
| chr10:113073868
|
G | A | 39 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0078others(36): Show | 39 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.552+33742G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073868 | ||||||
| chr10:113073920
|
C | T | 1 | a0001c0001t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.552+33794C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113073920 | ||||||
| chr10:113074025
|
G | A | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.552+33899G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074025 | ||||||
| chr10:113074058
|
G | C | 1 | a0002c0002t0007g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.552+33932G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074058 | ||||||
| chr10:113074091
|
C | T | 35 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.552+33965C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074091 | ||||||
| chr10:113074456
|
G | A | 1 | a0001c0001t0009g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.552+34330G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074456 | ||||||
| chr10:113074463
|
A | C | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.552+34337A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074463 | ||||||
| chr10:113074565
|
G | A | 1 | a0001c0001t0011g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.552+34439G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074565 | ||||||
| chr10:113074573
|
A | G | 4 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0002g0158others(1): Show | 4 | HG02559.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+34447A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074573 | ||||||
| chr10:113074691
|
A | G | 1 | a0007c0008t0002g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.552+34565A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074691 | ||||||
| chr10:113074739
|
G | A | 130 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0044others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.552+34613G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074739 | ||||||
| chr10:113074832
|
C | T | 1 | a0001c0001t0008g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.552+34706C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074832 | ||||||
| chr10:113074873
|
G | C | 139 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0038others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.552+34747G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113074873 | ||||||
| chr10:113075003
|
G | GTATT | 8 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+34896_552+3489 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113075003 | |||||
| chr10:113075062
|
C | A | 34 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.552+34936C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075062 | ||||||
| chr10:113075174
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.552+35048T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075174 | ||||||
| chr10:113075230
|
G | A | 6 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0004g0016others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+35104G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075230 | ||||||
| chr10:113075315
|
C | T | 2 | a0001c0001t0006g0136a0001c0005t0006g0138 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552+35189C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075315 | ||||||
| chr10:113075466
|
A | AAAAAG | 198 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.552+35345_552+3534 others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113075466 | |||||
| chr10:113075693
|
G | A | 78 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0047others(75): Show | 78 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(75): Show |
intron_variant | MODIFIER | c.552+35567G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075693 | ||||||
| chr10:113075758
|
T | G | 1 | a0001c0001t0001g0017 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.552+35632T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075758 | ||||||
| chr10:113075915
|
C | T | 34 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.552+35789C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075915 | ||||||
| chr10:113075928
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0193a0001c0001t0001g0196others(5): Show | 8 | HG00280.hp1 HG00735.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+35802G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075928 | ||||||
| chr10:113075962
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.552+35836C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113075962 | ||||||
| chr10:113076007
|
G | A | 21 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(18): Show | 21 | HG00323.hp2 HG01099.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.552+35881G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076007 | ||||||
| chr10:113076093
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.552+35967G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076093 | ||||||
| chr10:113076135
|
C | CA | 52 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0046others(49): Show | 52 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.552+36031dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113076135 | |||||
| chr10:113076135
|
C | CAA | 11 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0173others(8): Show | 11 | HG01884.hp1 HG01981.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.552+36030_552+3603 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113076135 | |||||
| chr10:113076135
|
CA | C | 8 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(5): Show | 8 | HG01109.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+36031delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113076135 | |||||
| chr10:113076197
|
A | G | 129 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0044others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.552+36071A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076197 | ||||||
| chr10:113076231
|
G | A | 26 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0078others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.552+36105G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076231 | ||||||
| chr10:113076277
|
A | G | 8 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+36151A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076277 | ||||||
| chr10:113076422
|
A | G | 3 | a0001c0001t0002g0143a0001c0001t0005g0072a0001c0001t0012g0169 | 3 | HG00741.hp1 HG01106.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.552+36296A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076422 | ||||||
| chr10:113076445
|
TTTG | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0002g0158others(1): Show | 4 | HG02559.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+36331_552+3633 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113076445 | |||||
| chr10:113076542
|
C | T | 3 | a0001c0001t0005g0033a0001c0001t0005g0064a0001c0001t0007g0189 | 3 | HG03942.hp1 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.552+36416C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076542 | ||||||
| chr10:113076712
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.552+36586T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076712 | ||||||
| chr10:113076782
|
C | T | 1 | a0001c0001t0013g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.552+36656C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076782 | ||||||
| chr10:113076815
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.552+36689A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113076815 | ||||||
| chr10:113077073
|
G | T | 2 | a0001c0001t0001g0068a0003c0003t0032g0011 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.552+36947G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077073 | ||||||
| chr10:113077104
|
G | A | 5 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+36978G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077104 | ||||||
| chr10:113077116
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0004g0016others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+36990C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077116 | ||||||
| chr10:113077367
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0042g0177 | 2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.552+37241C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077367 | ||||||
| chr10:113077368
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0004g0126a0001c0001t0006g0157others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+37242A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077368 | ||||||
| chr10:113077493
|
C | T | 4 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0004g0016others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+37367C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077493 | ||||||
| chr10:113077504
|
C | T | 43 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.552+37378C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077504 | ||||||
| chr10:113077689
|
C | CT | 126 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0044others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.552+37567dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077689 | |||||
| chr10:113077702
|
C | CT | 55 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0040others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.552+37592dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077702 | |||||
| chr10:113077702
|
C | CTTT | 8 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+37590_552+3759 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077702 | |||||
| chr10:113077702
|
CT | C | 6 | a0001c0001t0001g0051a0001c0001t0003g0170a0001c0001t0013g0103others(3): Show | 6 | HG01070.hp1 HG01099.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.552+37592delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077702 | |||||
| chr10:113077816
|
T | C | 126 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0044others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.552+37690T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113077816 | ||||||
| chr10:113077858
|
C | CTTAT | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0066others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+37778_552+3778 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077858 | |||||
| chr10:113077858
|
CTTAT | C | 69 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0038others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.552+37778_552+3778 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077858 | |||||
| chr10:113077858
|
CTTATTTA others(1): Show |
C | 23 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0087others(20): Show | 23 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.552+37774_552+3778 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077858 | |||||
| chr10:113077858
|
CTTATTTA others(5): Show |
C | 19 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0001g0086others(16): Show | 19 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.552+37770_552+3778 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077858 | |||||
| chr10:113077858
|
CTTATTTA others(9): Show |
C | 23 | a0001c0001t0001g0062a0001c0001t0001g0068a0001c0001t0001g0074others(20): Show | 23 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.552+37766_552+3778 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077858 | |||||
| chr10:113077858
|
CTTATTTA others(13): Show |
C | 8 | a0001c0001t0002g0113a0001c0001t0004g0075a0001c0001t0017g0052others(5): Show | 8 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+37762_552+3778 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113077858 | |||||
| chr10:113078131
|
T | TA | 122 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0034others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.552+38016dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113078131 | |||||
| chr10:113078169
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0014g0153 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.552+38043T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113078169 | ||||||
| chr10:113078239
|
A | C | 5 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+38113A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113078239 | ||||||
| chr10:113078253
|
G | C | 8 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+38127G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113078253 | ||||||
| chr10:113078264
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.552+38138A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113078264 | ||||||
| chr10:113078434
|
T | C | 2 | a0001c0001t0002g0012a0001c0001t0042g0177 | 2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.552+38308T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113078434 | ||||||
| chr10:113078520
|
G | C | 39 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.552+38394G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113078520 | ||||||
| chr10:113078859
|
A | G | 8 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+38733A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113078859 | ||||||
| chr10:113079100
|
C | A | 1 | a0007c0008t0002g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.552+38974C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113079100 | ||||||
| chr10:113079113
|
C | T | 77 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0047others(74): Show | 77 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.552+38987C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113079113 | ||||||
| chr10:113079558
|
C | G | 5 | a0001c0001t0001g0079a0001c0001t0010g0098a0001c0001t0026g0124others(2): Show | 5 | HG02145.hp2 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+39432C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113079558 | ||||||
| chr10:113079750
|
C | T | 1 | a0001c0001t0012g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.552+39624C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113079750 | ||||||
| chr10:113079787
|
AG | A | 3 | a0001c0001t0006g0140a0001c0001t0006g0188a0001c0001t0010g0127 | 3 | HG01243.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.552+39662delG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113079787 | ||||||
| chr10:113079860
|
G | A | 8 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+39734G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113079860 | ||||||
| chr10:113079957
|
G | A | 39 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.552+39831G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113079957 | ||||||
| chr10:113080011
|
T | A | 46 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0078others(43): Show | 46 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.552+39885T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113080011 | ||||||
| chr10:113080285
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.552+40159G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113080285 | ||||||
| chr10:113080286
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.552+40160A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113080286 | ||||||
| chr10:113080735
|
G | A | 47 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.552+40609G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113080735 | ||||||
| chr10:113080857
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0016g0024a0002c0002t0001g0021 | 3 | HG02132.hp1 NA18964.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.552+40731A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113080857 | ||||||
| chr10:113080880
|
G | A | 47 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.552+40754G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113080880 | ||||||
| chr10:113080986
|
C | G | 34 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(31): Show | 34 | HG00323.hp2 HG01099.hp2 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.552+40860C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113080986 | ||||||
| chr10:113081271
|
T | G | 5 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+41145T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113081271 | ||||||
| chr10:113081707
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0002g0128 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.552+41581C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113081707 | ||||||
| chr10:113081857
|
C | T | 129 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0044others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.552+41731C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113081857 | ||||||
| chr10:113081899
|
A | G | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.552+41773A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113081899 | ||||||
| chr10:113082131
|
A | AT | 29 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(26): Show | 29 | HG00323.hp2 HG01099.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.552+42021dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113082131 | |||||
| chr10:113082131
|
A | ATT | 6 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0002g0158others(3): Show | 6 | HG02559.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.552+42020_552+4202 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113082131 | |||||
| chr10:113082131
|
AT | A | 34 | a0001c0001t0001g0019a0001c0001t0001g0056a0001c0001t0001g0089others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.552+42021delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113082131 | |||||
| chr10:113082265
|
C | G | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.552+42139C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082265 | ||||||
| chr10:113082343
|
A | AATT | 168 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0031others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.552+42220_552+4222 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113082343 | |||||
| chr10:113082437
|
C | G | 22 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0040others(19): Show | 22 | HG00597.hp2 HG01109.hp2 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.552+42311C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082437 | ||||||
| chr10:113082484
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.552+42358G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082484 | ||||||
| chr10:113082597
|
T | TTG | 11 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0193others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.552+42492_552+4249 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113082597 | |||||
| chr10:113082616
|
T | C | 4 | a0001c0001t0002g0012a0001c0001t0004g0126a0001c0001t0006g0157others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+42490T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082616 | ||||||
| chr10:113082631
|
G | A | 47 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.552+42505G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082631 | ||||||
| chr10:113082635
|
A | G | 2 | a0001c0001t0006g0188a0001c0001t0010g0127 | 2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.552+42509A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082635 | ||||||
| chr10:113082952
|
C | T | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.552+42826C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082952 | ||||||
| chr10:113082965
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0014g0153 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.552+42839G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113082965 | ||||||
| chr10:113083163
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.552+43037T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113083163 | ||||||
| chr10:113083164
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.552+43038G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113083164 | ||||||
| chr10:113083259
|
G | GAC | 46 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0060others(43): Show | 46 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.552+43166_552+4316 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
G | GACAC | 37 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0056others(34): Show | 37 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.552+43164_552+4316 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
G | GACACAC | 49 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0040others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.552+43162_552+4316 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
G | GACACACA others(1): Show |
12 | a0001c0001t0001g0019a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.552+43160_552+4316 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
G | GACACACA others(3): Show |
7 | a0001c0001t0001g0079a0001c0001t0001g0130a0001c0001t0002g0006others(4): Show | 7 | HG01243.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+43158_552+4316 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
G | GACACACA others(9): Show |
1 | a0001c0001t0012g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.552+43152_552+4316 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
GAC | G | 2 | a0001c0001t0001g0029a0001c0001t0007g0020 | 2 | HG02132.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.552+43166_552+4316 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
GACAC | G | 15 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0051others(12): Show | 15 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.552+43164_552+4316 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
GACACACA others(1): Show |
G | 3 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0002g0095 | 3 | HG01981.hp2 HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.552+43160_552+4316 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083259
|
GACACACA others(5): Show |
G | 5 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+43156_552+4316 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113083259 | |||||
| chr10:113083465
|
C | G | 4 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0004g0016others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+43339C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113083465 | ||||||
| chr10:113083531
|
A | G | 8 | a0001c0001t0002g0107a0001c0001t0003g0163a0001c0001t0007g0020others(5): Show | 8 | HG00099.hp1 HG00140.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+43405A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113083531 | ||||||
| chr10:113083779
|
A | G | 2 | a0001c0001t0006g0136a0001c0005t0006g0138 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.552+43653A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113083779 | ||||||
| chr10:113083873
|
A | G | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.552+43747A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113083873 | ||||||
| chr10:113084163
|
T | C | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.552+44037T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084163 | ||||||
| chr10:113084190
|
G | A | 18 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0040others(15): Show | 18 | HG00597.hp2 HG01978.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.552+44064G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084190 | ||||||
| chr10:113084498
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0016g0024a0002c0002t0001g0021 | 3 | HG02132.hp1 NA18964.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.552+44372C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084498 | ||||||
| chr10:113084676
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.552+44550C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084676 | ||||||
| chr10:113084751
|
A | T | 18 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0040others(15): Show | 18 | HG00597.hp2 HG01978.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.552+44625A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084751 | ||||||
| chr10:113084755
|
G | A | 2 | a0001c0001t0004g0132a0001c0001t0005g0054 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.552+44629G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084755 | ||||||
| chr10:113084820
|
C | T | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.552+44694C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084820 | ||||||
| chr10:113084909
|
C | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0002g0158others(1): Show | 4 | HG02559.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+44783C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084909 | ||||||
| chr10:113084910
|
C | A | 33 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(30): Show | 33 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.552+44784C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084910 | ||||||
| chr10:113084910
|
C | CA | 7 | a0001c0001t0001g0066a0001c0001t0005g0199a0001c0001t0011g0159others(4): Show | 7 | HG01175.hp2 HG01496.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+44796dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113084910 | |||||
| chr10:113084911
|
A | C | 2 | a0001c0001t0001g0086a0001c0001t0014g0055 | 2 | HG01981.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.552+44785A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084911 | ||||||
| chr10:113084912
|
A | C | 3 | a0001c0001t0006g0140a0001c0001t0006g0188a0001c0001t0010g0127 | 3 | HG01243.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.552+44786A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084912 | ||||||
| chr10:113084992
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0014g0153 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.552+44866C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113084992 | ||||||
| chr10:113085025
|
T | G | 1 | a0001c0001t0007g0085 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.552+44899T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085025 | ||||||
| chr10:113085226
|
A | AT | 26 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0040others(23): Show | 26 | HG00597.hp2 HG01109.hp2 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.552+45116dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113085226 | |||||
| chr10:113085226
|
AT | A | 36 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(33): Show | 36 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.552+45116delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113085226 | |||||
| chr10:113085305
|
A | G | 4 | a0001c0001t0004g0134a0001c0001t0006g0005a0001c0001t0011g0175others(1): Show | 4 | HG01081.hp1 HG02055.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+45179A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085305 | ||||||
| chr10:113085344
|
A | G | 4 | a0001c0001t0006g0007a0001c0001t0011g0159a0001c0001t0014g0083others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+45218A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085344 | ||||||
| chr10:113085523
|
C | T | 3 | a0001c0001t0006g0140a0001c0001t0006g0188a0001c0001t0010g0127 | 3 | HG01243.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.552+45397C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085523 | ||||||
| chr10:113085541
|
G | A | 9 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0132others(6): Show | 9 | HG02622.hp2 HG02717.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.552+45415G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085541 | ||||||
| chr10:113085611
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0004g0126a0001c0001t0006g0157others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+45485C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085611 | ||||||
| chr10:113085620
|
C | A | 2 | a0001c0001t0001g0129a0001c0001t0014g0153 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.552+45494C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085620 | ||||||
| chr10:113085994
|
G | A | 5 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552+45868G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113085994 | ||||||
| chr10:113086018
|
G | A | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.552+45892G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113086018 | ||||||
| chr10:113086141
|
C | T | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.552+46015C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113086141 | ||||||
| chr10:113086575
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.552+46449G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113086575 | ||||||
| chr10:113086773
|
A | AAG | 8 | a0001c0001t0002g0102a0001c0001t0003g0186a0001c0001t0005g0122others(5): Show | 8 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+46648_552+4664 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113086773 | |||||
| chr10:113086773
|
A | AG | 111 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0036others(108): Show | 111 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.552+46647_552+4664 others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113086773 | ||||||
| chr10:113086773
|
A | G | 50 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0038others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.552+46647A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113086773 | ||||||
| chr10:113086802
|
A | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+46676A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113086802 | ||||||
| chr10:113086890
|
A | G | 39 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0078others(36): Show | 39 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.552+46764A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113086890 | ||||||
| chr10:113087006
|
GA | G | 4 | a0001c0001t0006g0140a0001c0001t0006g0188a0001c0001t0010g0127others(1): Show | 4 | HG01243.hp2 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+46890delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113087006 | |||||
| chr10:113087007
|
A | G | 45 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.552+46881A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087007 | ||||||
| chr10:113087032
|
C | A | 2 | a0001c0001t0002g0155a0007c0008t0002g0015 | 2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.552+46906C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087032 | ||||||
| chr10:113087161
|
T | C | 2 | a0002c0002t0001g0028a0002c0002t0007g0030 | 2 | HG02683.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.552+47035T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087161 | ||||||
| chr10:113087187
|
G | C | 1 | a0001c0001t0006g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.552+47061G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087187 | ||||||
| chr10:113087379
|
C | T | 1 | a0001c0001t0006g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.552+47253C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087379 | ||||||
| chr10:113087384
|
A | T | 23 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0125others(20): Show | 23 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.552+47258A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087384 | ||||||
| chr10:113087421
|
A | T | 1 | a0001c0001t0004g0016 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.552+47295A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087421 | ||||||
| chr10:113087621
|
C | A | 1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.552+47495C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087621 | ||||||
| chr10:113087685
|
T | TG | 50 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0038others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.552+47564dupG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113087685 | |||||
| chr10:113087964
|
A | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0041others(14): Show | 17 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.552+47838A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113087964 | ||||||
| chr10:113088146
|
T | A | 24 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(21): Show | 24 | HG00323.hp2 HG01099.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.552+48020T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088146 | ||||||
| chr10:113088224
|
A | T | 7 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+48098A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088224 | ||||||
| chr10:113088464
|
T | C | 4 | a0001c0001t0006g0136a0001c0005t0006g0138a0001c0005t0019g0001others(1): Show | 4 | HG02896.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+48338T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088464 | ||||||
| chr10:113088605
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0004g0126a0001c0001t0006g0157others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+48479A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088605 | ||||||
| chr10:113088631
|
G | C | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552+48505G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088631 | ||||||
| chr10:113088648
|
G | T | 18 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0040others(15): Show | 18 | HG00597.hp2 HG02040.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.552+48522G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088648 | ||||||
| chr10:113088688
|
G | A | 1 | a0001c0001t0004g0016 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.552+48562G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088688 | ||||||
| chr10:113088800
|
A | AG | 7 | a0001c0001t0001g0079a0001c0001t0009g0080a0001c0001t0010g0098others(4): Show | 7 | HG02109.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.552+48674_552+4867 others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088800 | ||||||
| chr10:113088912
|
C | T | 1 | a0001c0001t0030g0004 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.552+48786C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088912 | ||||||
| chr10:113088929
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0004g0126a0001c0001t0006g0157others(1): Show | 4 | HG01884.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.552+48803C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088929 | ||||||
| chr10:113088988
|
G | A | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.552+48862G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113088988 | ||||||
| chr10:113089213
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.552+49087C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089213 | ||||||
| chr10:113089290
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.552+49164A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089290 | ||||||
| chr10:113089347
|
G | A | 1 | a0001c0001t0014g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.552+49221G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089347 | ||||||
| chr10:113089358
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.552+49232G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089358 | ||||||
| chr10:113089594
|
C | T | 55 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0046others(52): Show | 55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.552+49468C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089594 | ||||||
| chr10:113089595
|
G | A | 3 | a0001c0001t0011g0175a0001c0001t0011g0184a0001c0001t0014g0055 | 3 | HG01081.hp1 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.552+49469G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089595 | ||||||
| chr10:113089640
|
C | T | 16 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.552+49514C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089640 | ||||||
| chr10:113089822
|
A | G | 1 | a0001c0001t0004g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.552+49696A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089822 | ||||||
| chr10:113089881
|
G | A | 3 | a0001c0001t0031g0010a0001c0004t0013g0145a0003c0003t0020g0135 | 3 | HG02280.hp1 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.552+49755G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089881 | ||||||
| chr10:113089922
|
T | C | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552+49796T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089922 | ||||||
| chr10:113089968
|
G | T | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.552+49842G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113089968 | ||||||
| chr10:113090088
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.552+49962T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090088 | ||||||
| chr10:113090288
|
G | A | 14 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(11): Show | 14 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.552+50162G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090288 | ||||||
| chr10:113090403
|
G | C | 1 | a0001c0001t0002g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.552+50277G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090403 | ||||||
| chr10:113090561
|
A | G | 2 | a0001c0001t0001g0130a0007c0008t0002g0015 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.552+50435A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090561 | ||||||
| chr10:113090671
|
C | T | 9 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(6): Show | 9 | HG02257.hp1 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-50513C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090671 | ||||||
| chr10:113090713
|
G | A | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.553-50471G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090713 | ||||||
| chr10:113090718
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.553-50466G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090718 | ||||||
| chr10:113090886
|
G | A | 1 | a0001c0001t0012g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.553-50298G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113090886 | ||||||
| chr10:113091045
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.553-50139G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091045 | ||||||
| chr10:113091101
|
C | T | 4 | a0001c0001t0002g0012a0001c0001t0004g0075a0001c0001t0013g0151others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-50083C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091101 | ||||||
| chr10:113091191
|
C | A | 5 | a0001c0001t0001g0068a0001c0001t0002g0094a0001c0001t0004g0132others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-49993C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091191 | ||||||
| chr10:113091192
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0004g0075a0001c0001t0013g0151 | 3 | HG01884.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.553-49992G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091192 | ||||||
| chr10:113091192
|
G | C | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.553-49992G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091192 | ||||||
| chr10:113091387
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-49797T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091387 | ||||||
| chr10:113091405
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.553-49779G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091405 | ||||||
| chr10:113091457
|
G | C | 3 | a0001c0001t0006g0188a0001c0001t0008g0148a0001c0001t0010g0127 | 3 | HG01243.hp2 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.553-49727G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091457 | ||||||
| chr10:113091514
|
C | T | 1 | a0001c0001t0012g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.553-49670C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091514 | ||||||
| chr10:113091589
|
T | C | 3 | a0001c0001t0004g0141a0001c0001t0006g0136a0001c0005t0006g0138 | 3 | HG02486.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.553-49595T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091589 | ||||||
| chr10:113091595
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-49589T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091595 | ||||||
| chr10:113091721
|
A | G | 1 | a0001c0001t0009g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.553-49463A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091721 | ||||||
| chr10:113091867
|
G | C | 4 | a0001c0001t0002g0012a0001c0001t0004g0075a0001c0001t0013g0151others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-49317G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113091867 | ||||||
| chr10:113092339
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.553-48845C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113092339 | ||||||
| chr10:113092849
|
G | A | 1 | a0001c0001t0006g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.553-48335G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113092849 | ||||||
| chr10:113092969
|
C | A | 1 | a0001c0001t0004g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.553-48215C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113092969 | ||||||
| chr10:113093093
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.553-48091G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113093093 | ||||||
| chr10:113093166
|
T | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(6): Show | 9 | HG02257.hp1 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-48018T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113093166 | ||||||
| chr10:113093349
|
GGGCCATG others(6): Show |
G | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.553-47810_553-4779 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113093349 | |||||
| chr10:113093375
|
T | C | 2 | a0001c0001t0002g0142a0001c0001t0002g0155 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.553-47809T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113093375 | ||||||
| chr10:113094004
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.553-47180G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113094004 | ||||||
| chr10:113094088
|
C | T | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.553-47096C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113094088 | ||||||
| chr10:113094403
|
A | G | 10 | a0001c0001t0001g0197a0001c0001t0002g0102a0001c0001t0003g0186others(7): Show | 10 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.553-46781A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113094403 | ||||||
| chr10:113094567
|
T | G | 3 | a0001c0001t0002g0113a0001c0001t0003g0179a0001c0001t0036g0116 | 3 | HG00741.hp2 HG01256.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.553-46617T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113094567 | ||||||
| chr10:113094624
|
C | T | 26 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0047others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.553-46560C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113094624 | ||||||
| chr10:113094962
|
A | T | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-46222A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113094962 | ||||||
| chr10:113095218
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.553-45966T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113095218 | ||||||
| chr10:113095306
|
G | A | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.553-45878G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113095306 | ||||||
| chr10:113095485
|
C | T | 1 | a0001c0001t0004g0016 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.553-45699C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113095485 | ||||||
| chr10:113095594
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.553-45590A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113095594 | ||||||
| chr10:113095638
|
C | T | 65 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0056others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.553-45546C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113095638 | ||||||
| chr10:113096076
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0005g0054 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.553-45108C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113096076 | ||||||
| chr10:113096122
|
A | G | 3 | a0001c0001t0004g0141a0001c0001t0006g0136a0001c0005t0006g0138 | 3 | HG02486.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.553-45062A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113096122 | ||||||
| chr10:113096127
|
T | C | 12 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(9): Show | 12 | HG02257.hp1 HG02486.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.553-45057T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113096127 | ||||||
| chr10:113096260
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.553-44924G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113096260 | ||||||
| chr10:113096353
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.553-44831A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113096353 | ||||||
| chr10:113096604
|
C | T | 4 | a0001c0001t0004g0134a0001c0001t0011g0175a0001c0001t0011g0176others(1): Show | 4 | HG01081.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-44580C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113096604 | ||||||
| chr10:113096767
|
G | T | 24 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(21): Show | 24 | HG00408.hp2 HG00597.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.553-44417G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113096767 | ||||||
| chr10:113097321
|
C | G | 1 | a0001c0001t0006g0013 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.553-43863C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097321 | ||||||
| chr10:113097424
|
G | A | 57 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0056others(54): Show | 57 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.553-43760G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097424 | ||||||
| chr10:113097644
|
C | CG | 4 | a0001c0001t0001g0068a0001c0001t0001g0125a0001c0005t0019g0001others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-43538dupG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097644 | |||||
| chr10:113097646
|
G | GA | 17 | a0001c0001t0001g0066a0001c0001t0001g0131a0001c0001t0001g0190others(14): Show | 17 | HG01515.hp1 HG01884.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.553-43510dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097646 | |||||
| chr10:113097646
|
G | GAAAAAAA others(17): Show |
1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.553-43531_553-4353 others(28): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097646 | |||||
| chr10:113097646
|
G | GGA | 3 | a0001c0001t0011g0175a0001c0001t0011g0176a0001c0001t0011g0184 | 3 | HG01081.hp1 HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.553-43538_553-4353 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097646 | ||||||
| chr10:113097646
|
GA | G | 62 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0044others(59): Show | 62 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.553-43510delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097646 | |||||
| chr10:113097646
|
GAA | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0041a0001c0001t0001g0193others(6): Show | 9 | HG00280.hp1 HG00642.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-43511_553-4351 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097646 | |||||
| chr10:113097646
|
GAAAAAAA others(6): Show |
G | 6 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0002g0118others(3): Show | 6 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-43522_553-4351 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097646 | |||||
| chr10:113097647
|
A | G | 7 | a0001c0001t0001g0129a0001c0001t0002g0094a0001c0001t0004g0126others(4): Show | 7 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-43537A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097647 | ||||||
| chr10:113097648
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.553-43536A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097648 | ||||||
| chr10:113097654
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0029g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.553-43523_553-4352 others(26): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097654 | |||||
| chr10:113097654
|
A | AAAAAAAC others(14): Show |
3 | a0001c0001t0001g0074a0001c0001t0001g0123a0001c0001t0004g0133 | 3 | HG02818.hp2 HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.553-43524_553-4352 others(25): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097654 | |||||
| chr10:113097654
|
A | AAAAAAAC others(13): Show |
3 | a0001c0001t0033g0003a0001c0001t0046g0152a0001c0001t0047g0150 | 3 | HG02257.hp1 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.553-43524_553-4352 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097654 | |||||
| chr10:113097654
|
A | AAAAAAAC others(14): Show |
1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.553-43524_553-4352 others(25): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097654 | |||||
| chr10:113097654
|
A | C | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.553-43530A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097654 | ||||||
| chr10:113097667
|
AAAAAAAA others(1): Show |
A | 7 | a0001c0001t0001g0197a0001c0001t0002g0102a0001c0001t0003g0186others(4): Show | 7 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-43514_553-4350 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113097667 | |||||
| chr10:113097669
|
A | T | 2 | a0001c0001t0010g0111a0001c0001t0015g0008 | 2 | HG01433.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.553-43515A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097669 | ||||||
| chr10:113097670
|
A | C | 1 | a0002c0002t0001g0088 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.553-43514A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097670 | ||||||
| chr10:113097919
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.553-43265G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097919 | ||||||
| chr10:113097964
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.553-43220C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113097964 | ||||||
| chr10:113098049
|
C | CA | 6 | a0001c0001t0001g0066a0001c0001t0001g0079a0001c0001t0001g0131others(3): Show | 6 | HG01175.hp1 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-43111dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113098049 | |||||
| chr10:113098049
|
CA | C | 101 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0048others(98): Show | 101 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.553-43111delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113098049 | |||||
| chr10:113098049
|
CAA | C | 5 | a0001c0001t0001g0044a0001c0001t0017g0071a0001c0001t0043g0168others(2): Show | 5 | HG00323.hp2 HG01433.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-43112_553-4311 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113098049 | |||||
| chr10:113098071
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.553-43113A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113098071 | ||||||
| chr10:113098299
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0196 | 2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.553-42885C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113098299 | ||||||
| chr10:113098575
|
G | A | 1 | a0001c0001t0015g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.553-42609G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113098575 | ||||||
| chr10:113098678
|
C | G | 2 | a0001c0001t0001g0131a0001c0001t0002g0117 | 2 | HG01515.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.553-42506C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113098678 | ||||||
| chr10:113098803
|
C | T | 4 | a0001c0001t0004g0134a0001c0001t0011g0175a0001c0001t0011g0176others(1): Show | 4 | HG01081.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-42381C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113098803 | ||||||
| chr10:113098852
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.553-42332A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113098852 | ||||||
| chr10:113098920
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0004g0075a0001c0001t0013g0151others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-42264A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113098920 | ||||||
| chr10:113099030
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.553-42154G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099030 | ||||||
| chr10:113099163
|
CAAGCTAA others(15): Show |
C | 31 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0047others(28): Show | 31 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.553-42017_553-4199 others(26): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113099163 | |||||
| chr10:113099395
|
C | T | 12 | a0001c0001t0001g0130a0001c0001t0001g0197a0001c0001t0002g0102others(9): Show | 12 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.553-41789C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099395 | ||||||
| chr10:113099405
|
G | T | 135 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0038others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.553-41779G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099405 | ||||||
| chr10:113099492
|
A | G | 178 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.553-41692A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099492 | ||||||
| chr10:113099655
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.553-41529C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099655 | ||||||
| chr10:113099657
|
C | G | 68 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0046others(65): Show | 68 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.553-41527C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099657 | ||||||
| chr10:113099676
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.553-41508C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099676 | ||||||
| chr10:113099704
|
G | A | 135 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0038others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.553-41480G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099704 | ||||||
| chr10:113099708
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.553-41476G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113099708 | ||||||
| chr10:113100069
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.553-41115C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100069 | ||||||
| chr10:113100106
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.553-41078A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100106 | ||||||
| chr10:113100217
|
C | T | 3 | a0001c0001t0004g0141a0001c0001t0006g0136a0001c0005t0006g0138 | 3 | HG02486.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.553-40967C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100217 | ||||||
| chr10:113100256
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0006g0137 | 3 | HG03195.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.553-40928A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100256 | ||||||
| chr10:113100437
|
G | A | 9 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(6): Show | 9 | HG02257.hp1 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-40747G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100437 | ||||||
| chr10:113100481
|
AT | A | 12 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(9): Show | 12 | HG02257.hp1 HG02486.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.553-40691delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113100481 | |||||
| chr10:113100621
|
G | A | 4 | a0001c0001t0004g0134a0001c0001t0011g0175a0001c0001t0011g0176others(1): Show | 4 | HG01081.hp1 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-40563G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100621 | ||||||
| chr10:113100736
|
A | T | 1 | a0001c0001t0003g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.553-40448A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100736 | ||||||
| chr10:113100891
|
C | A | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-40293C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100891 | ||||||
| chr10:113100900
|
A | G | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-40284A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100900 | ||||||
| chr10:113100920
|
A | T | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-40264A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113100920 | ||||||
| chr10:113101060
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-40124A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101060 | ||||||
| chr10:113101063
|
G | T | 2 | a0001c0001t0002g0142a0001c0001t0002g0155 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.553-40121G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101063 | ||||||
| chr10:113101071
|
G | A | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-40113G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101071 | ||||||
| chr10:113101083
|
G | GA | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-40095dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113101083 | |||||
| chr10:113101085
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.553-40099A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101085 | ||||||
| chr10:113101195
|
C | G | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.553-39989C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101195 | ||||||
| chr10:113101473
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.553-39711T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101473 | ||||||
| chr10:113101545
|
A | G | 30 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0047others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-39639A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101545 | ||||||
| chr10:113101616
|
G | C | 57 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0056others(54): Show | 57 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.553-39568G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101616 | ||||||
| chr10:113101617
|
C | T | 1 | a0001c0001t0007g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.553-39567C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101617 | ||||||
| chr10:113101715
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.553-39469C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101715 | ||||||
| chr10:113101720
|
G | A | 4 | a0001c0001t0026g0124a0001c0004t0008g0144a0001c0004t0008g0146others(1): Show | 4 | HG01109.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-39464G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101720 | ||||||
| chr10:113101837
|
C | T | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-39347C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101837 | ||||||
| chr10:113101842
|
C | CAAAAAAA others(3): Show |
9 | a0001c0001t0001g0131a0001c0001t0002g0104a0001c0001t0002g0142others(6): Show | 9 | HG00323.hp1 HG01070.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-39336_553-3932 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113101842 | |||||
| chr10:113101842
|
C | CAAAAAAA others(4): Show |
111 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.553-39337_553-3932 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113101842 | |||||
| chr10:113101842
|
C | CAAAAAAA others(5): Show |
35 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0068others(32): Show | 35 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.553-39338_553-3932 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113101842 | |||||
| chr10:113101842
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0005g0199a0001c0001t0008g0092a0001c0001t0013g0151others(1): Show | 4 | HG02145.hp1 HG02559.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-39339_553-3932 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113101842 | |||||
| chr10:113101842
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.553-39340_553-3932 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113101842 | |||||
| chr10:113101856
|
A | AAAAAAAA others(4): Show |
1 | a0001c0004t0008g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.553-39327_553-3932 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113101856 | |||||
| chr10:113101858
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.553-39326G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113101858 | ||||||
| chr10:113102050
|
G | T | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-39134G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102050 | ||||||
| chr10:113102101
|
G | A | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.553-39083G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102101 | ||||||
| chr10:113102111
|
CA | C | 30 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(27): Show | 30 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-39042delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAA | C | 33 | a0001c0001t0001g0099a0001c0001t0001g0191a0001c0001t0001g0194others(30): Show | 33 | HG00735.hp2 HG01109.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.553-39043_553-3904 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAAA | C | 56 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0047others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.553-39044_553-3904 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAAAA | C | 37 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0056others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.553-39045_553-3904 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAAAAA | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(6): Show | 9 | HG01070.hp2 HG02257.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-39046_553-3904 others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0002g0107a0001c0001t0003g0163a0001c0001t0007g0020others(3): Show | 6 | HG00099.hp1 HG00140.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-39050_553-3904 others(13): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0012a0001c0001t0004g0075a0001c0001t0013g0151 | 3 | HG01884.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.553-39051_553-3904 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0130a0007c0008t0002g0015 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.553-39057_553-3904 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102111
|
CAAAAAAA others(12): Show |
C | 1 | a0002c0002t0003g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.553-39060_553-3904 others(23): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102111 | |||||
| chr10:113102114
|
A | C | 1 | a0001c0001t0042g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.553-39070A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102114 | ||||||
| chr10:113102115
|
A | C | 16 | a0001c0001t0001g0086a0001c0001t0001g0101a0001c0001t0002g0113others(13): Show | 16 | HG00597.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.553-39069A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102115 | ||||||
| chr10:113102116
|
A | C | 30 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0056others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-39068A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102116 | ||||||
| chr10:113102117
|
A | C | 1 | a0001c0001t0025g0035 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.553-39067A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102117 | ||||||
| chr10:113102131
|
A | C | 1 | a0002c0002t0003g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.553-39053A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102131 | ||||||
| chr10:113102321
|
T | A | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-38863T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102321 | ||||||
| chr10:113102427
|
G | GT | 13 | a0001c0001t0001g0068a0001c0001t0001g0082a0001c0001t0001g0125others(10): Show | 13 | HG01981.hp1 HG02145.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.553-38742dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113102427 | |||||
| chr10:113102430
|
T | TG | 2 | a0001c0001t0001g0060a0001c0001t0002g0113 | 2 | HG00741.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.553-38754_553-3875 others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102430 | ||||||
| chr10:113102431
|
T | G | 56 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0056others(53): Show | 56 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.553-38753T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102431 | ||||||
| chr10:113102456
|
G | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0115 | 2 | HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.553-38728G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102456 | ||||||
| chr10:113102981
|
C | G | 1 | a0001c0005t0006g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.553-38203C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102981 | ||||||
| chr10:113102998
|
T | C | 27 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(24): Show | 27 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.553-38186T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113102998 | ||||||
| chr10:113103006
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.553-38178A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113103006 | ||||||
| chr10:113103177
|
G | C | 7 | a0001c0001t0004g0134a0001c0001t0004g0141a0001c0001t0006g0136others(4): Show | 7 | HG01081.hp1 HG02486.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-38007G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113103177 | ||||||
| chr10:113103391
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0040g0164 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.553-37793G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113103391 | ||||||
| chr10:113103465
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.553-37719G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113103465 | ||||||
| chr10:113103499
|
A | G | 9 | a0001c0001t0001g0068a0001c0001t0001g0125a0001c0001t0001g0129others(6): Show | 9 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-37685A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113103499 | ||||||
| chr10:113103663
|
G | A | 1 | a0001c0001t0011g0176 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.553-37521G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113103663 | ||||||
| chr10:113103811
|
A | G | 1 | a0001c0001t0042g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.553-37373A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113103811 | ||||||
| chr10:113104002
|
G | A | 1 | a0001c0001t0009g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.553-37182G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113104002 | ||||||
| chr10:113104538
|
T | C | 3 | a0001c0001t0017g0052a0001c0001t0034g0187a0001c0001t0041g0180 | 3 | HG01071.hp1 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.553-36646T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113104538 | ||||||
| chr10:113104666
|
A | C | 19 | a0001c0001t0001g0130a0001c0001t0001g0197a0001c0001t0002g0102others(16): Show | 19 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.553-36518A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113104666 | ||||||
| chr10:113104779
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.553-36405C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113104779 | ||||||
| chr10:113105012
|
G | A | 2 | a0001c0001t0001g0130a0007c0008t0002g0015 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.553-36172G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105012 | ||||||
| chr10:113105097
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.553-36087G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105097 | ||||||
| chr10:113105346
|
C | G | 9 | a0001c0001t0001g0068a0001c0001t0001g0125a0001c0001t0001g0129others(6): Show | 9 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-35838C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105346 | ||||||
| chr10:113105386
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.553-35798G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105386 | ||||||
| chr10:113105435
|
T | C | 21 | a0001c0001t0001g0130a0001c0001t0001g0197a0001c0001t0002g0102others(18): Show | 21 | HG00140.hp1 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.553-35749T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105435 | ||||||
| chr10:113105442
|
G | A | 1 | a0002c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.553-35742G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105442 | ||||||
| chr10:113105450
|
G | A | 1 | a0001c0001t0043g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.553-35734G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105450 | ||||||
| chr10:113105473
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0002g0095 | 3 | HG01981.hp2 HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.553-35711A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105473 | ||||||
| chr10:113105622
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.553-35562C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105622 | ||||||
| chr10:113105623
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.553-35561C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105623 | ||||||
| chr10:113105730
|
C | T | 161 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0034others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.553-35454C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105730 | ||||||
| chr10:113105738
|
T | C | 28 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0130others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.553-35446T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105738 | ||||||
| chr10:113105881
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0002g0095 | 3 | HG01981.hp2 HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.553-35303T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113105881 | ||||||
| chr10:113106055
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0004g0126a0001c0001t0006g0137 | 3 | HG03195.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.553-35129T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106055 | ||||||
| chr10:113106320
|
G | A | 1 | a0001c0001t0007g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.553-34864G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106320 | ||||||
| chr10:113106393
|
C | G | 3 | a0001c0001t0004g0141a0001c0001t0006g0136a0001c0005t0006g0138 | 3 | HG02486.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.553-34791C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106393 | ||||||
| chr10:113106413
|
G | A | 26 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0047others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.553-34771G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106413 | ||||||
| chr10:113106868
|
C | A | 1 | a0001c0001t0003g0181 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.553-34316C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106868 | ||||||
| chr10:113106873
|
G | T | 58 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0056others(55): Show | 58 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.553-34311G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106873 | ||||||
| chr10:113106971
|
A | G | 3 | a0001c0001t0002g0142a0001c0001t0002g0155a0001c0001t0006g0157 | 3 | HG03209.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.553-34213A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106971 | ||||||
| chr10:113106990
|
C | G | 9 | a0001c0001t0001g0068a0001c0001t0001g0125a0001c0001t0001g0129others(6): Show | 9 | HG02622.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-34194C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113106990 | ||||||
| chr10:113107018
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-34166C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107018 | ||||||
| chr10:113107119
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.553-34065A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107119 | ||||||
| chr10:113107149
|
G | A | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.553-34035G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107149 | ||||||
| chr10:113107430
|
T | G | 1 | a0001c0001t0014g0153 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.553-33754T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107430 | ||||||
| chr10:113107525
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0015g0112 | 2 | HG01515.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.553-33659C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107525 | ||||||
| chr10:113107533
|
G | C | 9 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0123others(6): Show | 9 | HG02257.hp1 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-33651G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107533 | ||||||
| chr10:113107604
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0196 | 2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.553-33580G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107604 | ||||||
| chr10:113107612
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0026g0124a0001c0004t0008g0144others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-33572G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107612 | ||||||
| chr10:113107668
|
G | C | 12 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0058others(9): Show | 12 | HG00323.hp2 HG01123.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-33516G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107668 | ||||||
| chr10:113107686
|
CGAGCTTG others(4): Show |
C | 10 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0001g0086others(7): Show | 10 | HG00738.hp1 HG01070.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.553-33493_553-3348 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107686 | |||||
| chr10:113107697
|
TGA | T | 5 | a0001c0001t0006g0013a0001c0001t0008g0092a0001c0001t0008g0093others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-33485_553-3348 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107697 | |||||
| chr10:113107752
|
T | TA | 28 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0078others(25): Show | 28 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.553-33408dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAA | 32 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0036others(29): Show | 32 | HG00597.hp2 HG01081.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.553-33409_553-3340 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAAA | 9 | a0001c0001t0001g0040a0001c0001t0002g0173a0001c0001t0003g0174others(6): Show | 9 | HG01109.hp2 HG01978.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-33410_553-3340 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAAAAAA | 17 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0002g0102others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(14): Show |
intron_variant | MODIFIER | c.553-33413_553-3340 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAAAAAAA | 10 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0006g0149others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.553-33414_553-3340 others(11): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAAAAAAA others(1): Show |
6 | a0001c0001t0001g0048a0001c0001t0001g0074a0001c0001t0001g0099others(3): Show | 6 | HG01081.hp2 HG01258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-33415_553-3340 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAAAAAAA others(2): Show |
5 | a0001c0001t0001g0047a0001c0001t0010g0185a0001c0001t0012g0165others(2): Show | 5 | HG01256.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-33416_553-3340 others(13): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAAAAAAA others(3): Show |
3 | a0001c0001t0005g0067a0001c0001t0009g0057a0001c0001t0012g0154 | 3 | HG01123.hp2 HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.553-33417_553-3340 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0058 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.553-33419_553-3340 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107752
|
TA | T | 31 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0041others(28): Show | 31 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.553-33408delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113107752 | |||||
| chr10:113107774
|
A | C | 1 | a0001c0001t0006g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.553-33410A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107774 | ||||||
| chr10:113107777
|
C | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0058 | 2 | HG02055.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.553-33407C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113107777 | ||||||
| chr10:113108052
|
T | TC | 35 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0056others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.553-33130dupC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113108052 | |||||
| chr10:113108304
|
C | T | 6 | a0001c0001t0004g0134a0001c0001t0006g0013a0001c0001t0008g0092others(3): Show | 6 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-32880C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108304 | ||||||
| chr10:113108403
|
T | C | 28 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(25): Show | 28 | HG00408.hp2 HG00597.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.553-32781T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108403 | ||||||
| chr10:113108439
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0007g0020 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.553-32745C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108439 | ||||||
| chr10:113108593
|
C | T | 4 | a0001c0001t0002g0006a0001c0001t0006g0136a0001c0001t0045g0156others(1): Show | 4 | HG02109.hp2 HG02886.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-32591C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108593 | ||||||
| chr10:113108622
|
G | T | 2 | a0001c0001t0010g0098a0003c0003t0011g0009 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.553-32562G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108622 | ||||||
| chr10:113108818
|
C | A | 1 | a0001c0001t0006g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.553-32366C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108818 | ||||||
| chr10:113108819
|
A | G | 1 | a0002c0002t0007g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.553-32365A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108819 | ||||||
| chr10:113108993
|
A | G | 1 | a0001c0001t0006g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.553-32191A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113108993 | ||||||
| chr10:113109431
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.553-31753G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113109431 | ||||||
| chr10:113109613
|
A | G | 1 | a0001c0001t0044g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.553-31571A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113109613 | ||||||
| chr10:113109623
|
G | T | 1 | a0001c0001t0001g0031 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.553-31561G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113109623 | ||||||
| chr10:113109960
|
G | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0125others(13): Show | 16 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.553-31224G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113109960 | ||||||
| chr10:113109984
|
A | T | 1 | a0001c0001t0002g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.553-31200A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113109984 | ||||||
| chr10:113110002
|
C | T | 2 | a0001c0001t0031g0010a0004c0006t0001g0053 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.553-31182C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110002 | ||||||
| chr10:113110033
|
G | A | 34 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(31): Show | 34 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.553-31151G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110033 | ||||||
| chr10:113110107
|
C | A | 2 | a0001c0001t0010g0098a0003c0003t0011g0009 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.553-31077C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110107 | ||||||
| chr10:113110368
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0004g0133a0001c0001t0004g0141others(3): Show | 6 | HG02486.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-30816G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110368 | ||||||
| chr10:113110369
|
G | GT | 33 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(30): Show | 33 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.553-30794dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113110369 | |||||
| chr10:113110369
|
G | T | 6 | a0001c0001t0001g0079a0001c0001t0004g0097a0001c0001t0009g0080others(3): Show | 6 | HG02257.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-30815G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110369 | ||||||
| chr10:113110369
|
GT | G | 37 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0051others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.553-30794delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113110369 | |||||
| chr10:113110369
|
GTT | G | 86 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.553-30795_553-3079 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113110369 | |||||
| chr10:113110369
|
GTTT | G | 6 | a0001c0001t0003g0172a0001c0001t0006g0140a0001c0001t0007g0020others(3): Show | 6 | HG01943.hp1 HG03017.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-30796_553-3079 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113110369 | |||||
| chr10:113110514
|
C | T | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.553-30670C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110514 | ||||||
| chr10:113110663
|
G | C | 27 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0079others(24): Show | 27 | HG02145.hp1 HG02257.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.553-30521G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110663 | ||||||
| chr10:113110829
|
C | G | 4 | a0001c0001t0002g0113a0001c0001t0003g0179a0001c0001t0036g0116others(1): Show | 4 | HG00741.hp2 HG01256.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-30355C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110829 | ||||||
| chr10:113110872
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.553-30312A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110872 | ||||||
| chr10:113110927
|
G | A | 1 | a0001c0001t0003g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.553-30257G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113110927 | ||||||
| chr10:113111038
|
C | CT | 6 | a0001c0001t0001g0074a0001c0001t0004g0133a0001c0001t0004g0141others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-30131dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113111038 | |||||
| chr10:113111038
|
CT | C | 73 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0041others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.553-30131delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113111038 | |||||
| chr10:113111038
|
CTT | C | 50 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0056others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.553-30132_553-3013 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113111038 | |||||
| chr10:113111050
|
T | C | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.553-30134T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111050 | ||||||
| chr10:113111281
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-29903A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111281 | ||||||
| chr10:113111492
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.553-29692T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111492 | ||||||
| chr10:113111530
|
G | A | 1 | a0001c0001t0015g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.553-29654G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111530 | ||||||
| chr10:113111579
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.553-29605C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111579 | ||||||
| chr10:113111749
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.553-29435G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111749 | ||||||
| chr10:113111800
|
T | A | 107 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.553-29384T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111800 | ||||||
| chr10:113111801
|
A | AAAT | 3 | a0001c0001t0003g0172a0001c0001t0006g0140a0001c0001t0038g0106 | 3 | NA20129.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.553-29381_553-2938 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113111801 | |||||
| chr10:113111801
|
A | T | 107 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.553-29383A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111801 | ||||||
| chr10:113111835
|
A | G | 30 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0051others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.553-29349A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111835 | ||||||
| chr10:113111868
|
T | C | 16 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0125others(13): Show | 16 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.553-29316T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111868 | ||||||
| chr10:113111888
|
A | G | 7 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0082others(4): Show | 7 | HG00408.hp2 HG00597.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-29296A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111888 | ||||||
| chr10:113111936
|
G | A | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.553-29248G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113111936 | ||||||
| chr10:113112347
|
C | T | 3 | a0001c0001t0002g0107a0001c0001t0010g0111a0001c0001t0015g0008 | 3 | HG01346.hp1 HG01433.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.553-28837C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113112347 | ||||||
| chr10:113112369
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-28815C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113112369 | ||||||
| chr10:113112850
|
G | C | 6 | a0001c0001t0001g0074a0001c0001t0004g0133a0001c0001t0029g0114others(3): Show | 6 | HG02257.hp1 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-28334G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113112850 | ||||||
| chr10:113112908
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.553-28276G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113112908 | ||||||
| chr10:113113032
|
C | T | 1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.553-28152C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113032 | ||||||
| chr10:113113089
|
A | G | 2 | a0001c0001t0010g0111a0001c0001t0015g0008 | 2 | HG01433.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.553-28095A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113089 | ||||||
| chr10:113113280
|
G | A | 3 | a0001c0001t0017g0052a0001c0001t0034g0187a0001c0001t0041g0180 | 3 | HG01071.hp1 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.553-27904G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113280 | ||||||
| chr10:113113463
|
T | C | 14 | a0001c0001t0001g0129a0001c0001t0002g0012a0001c0001t0002g0142others(11): Show | 14 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-27721T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113463 | ||||||
| chr10:113113464
|
G | T | 14 | a0001c0001t0001g0129a0001c0001t0002g0012a0001c0001t0002g0142others(11): Show | 14 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-27720G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113464 | ||||||
| chr10:113113570
|
T | C | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.553-27614T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113570 | ||||||
| chr10:113113598
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-27586T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113598 | ||||||
| chr10:113113830
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-27354G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113830 | ||||||
| chr10:113113963
|
C | A | 68 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0041others(65): Show | 68 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.553-27221C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113963 | ||||||
| chr10:113113968
|
G | T | 78 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0056others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.553-27216G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113113968 | ||||||
| chr10:113114071
|
A | G | 19 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0001g0130others(16): Show | 19 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.553-27113A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113114071 | ||||||
| chr10:113114260
|
C | T | 157 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0036others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.553-26924C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113114260 | ||||||
| chr10:113114614
|
T | C | 109 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.553-26570T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113114614 | ||||||
| chr10:113114647
|
C | A | 27 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0074others(24): Show | 27 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.553-26537C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113114647 | ||||||
| chr10:113114898
|
G | C | 19 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0001g0130others(16): Show | 19 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.553-26286G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113114898 | ||||||
| chr10:113114968
|
G | C | 1 | a0007c0008t0002g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.553-26216G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113114968 | ||||||
| chr10:113115012
|
G | C | 24 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(21): Show | 24 | HG00408.hp2 HG01099.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.553-26172G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113115012 | ||||||
| chr10:113115212
|
C | A | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.553-25972C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113115212 | ||||||
| chr10:113115346
|
T | C | 19 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0001g0130others(16): Show | 19 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.553-25838T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113115346 | ||||||
| chr10:113115760
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.553-25424C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113115760 | ||||||
| chr10:113115763
|
G | A | 1 | a0003c0003t0032g0011 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.553-25421G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113115763 | ||||||
| chr10:113115795
|
C | T | 9 | a0001c0001t0001g0130a0001c0001t0006g0013a0001c0001t0008g0092others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-25389C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113115795 | ||||||
| chr10:113115917
|
G | A | 1 | a0003c0003t0020g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.553-25267G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113115917 | ||||||
| chr10:113116593
|
A | G | 1 | a0001c0001t0012g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.553-24591A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113116593 | ||||||
| chr10:113116647
|
C | T | 1 | a0001c0001t0038g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.553-24537C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113116647 | ||||||
| chr10:113117049
|
C | T | 2 | a0001c0001t0006g0005a0001c0001t0006g0140 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.553-24135C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117049 | ||||||
| chr10:113117306
|
G | A | 9 | a0001c0001t0001g0101a0001c0001t0004g0016a0001c0001t0004g0076others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-23878G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117306 | ||||||
| chr10:113117341
|
G | A | 9 | a0001c0001t0001g0101a0001c0001t0004g0016a0001c0001t0004g0076others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-23843G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117341 | ||||||
| chr10:113117361
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.553-23823G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117361 | ||||||
| chr10:113117363
|
TTTTCTCT others(25): Show |
T | 1 | a0001c0001t0042g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.553-23819_553-2378 others(36): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117363 | |||||
| chr10:113117364
|
TTTCTCTC others(10): Show |
T | 1 | a0001c0001t0011g0184 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.553-23818_553-2380 others(21): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117364 | |||||
| chr10:113117364
|
TTTCTCTC others(16): Show |
T | 1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.553-23818_553-2379 others(27): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117364 | |||||
| chr10:113117364
|
TTTCTCTC others(34): Show |
T | 1 | a0001c0001t0004g0126 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.553-23818_553-2377 others(45): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117364 | |||||
| chr10:113117364
|
TTTCTCTC others(36): Show |
T | 1 | a0001c0001t0002g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.553-23818_553-2377 others(47): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117364 | |||||
| chr10:113117364
|
TTTCTCTC others(38): Show |
T | 1 | a0001c0001t0002g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.553-23818_553-2377 others(49): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117364 | |||||
| chr10:113117364
|
TTTCTCTC others(40): Show |
T | 1 | a0001c0001t0007g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.553-23818_553-2377 others(51): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117364 | |||||
| chr10:113117367
|
C | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0107a0001c0001t0002g0158 | 3 | HG01346.hp1 HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.553-23817C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117367 | ||||||
| chr10:113117369
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0158 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.553-23815C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117369 | ||||||
| chr10:113117370
|
TCTCTCTC others(57): Show |
T | 1 | a0001c0001t0013g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.553-23789_553-2372 others(68): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117370 | |||||
| chr10:113117374
|
TCTCTCTC others(53): Show |
T | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-23785_553-2372 others(64): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117374 | |||||
| chr10:113117376
|
T | C | 7 | a0001c0001t0002g0094a0001c0001t0004g0141a0001c0001t0011g0176others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-23808T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117376 | ||||||
| chr10:113117376
|
TCTCTCTC others(51): Show |
T | 4 | a0001c0001t0006g0140a0001c0001t0006g0188a0001c0001t0008g0148others(1): Show | 4 | HG01243.hp2 HG02559.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-23783_553-2372 others(62): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117376 | |||||
| chr10:113117378
|
TCTCTCTC others(49): Show |
T | 2 | a0001c0001t0001g0017a0001c0001t0001g0196 | 2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.553-23781_553-2372 others(60): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117378 | |||||
| chr10:113117380
|
TCTCTCTC others(47): Show |
T | 3 | a0001c0001t0001g0193a0002c0002t0001g0090a0006c0012t0007g0026 | 3 | HG04228.hp1 NA18950.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.553-23779_553-2372 others(58): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117380 | |||||
| chr10:113117382
|
TCTCTCTC others(45): Show |
T | 3 | a0001c0001t0004g0134a0001c0001t0009g0045a0001c0001t0034g0187 | 3 | HG00280.hp1 HG01496.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.553-23777_553-2372 others(56): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117382 | |||||
| chr10:113117384
|
TCTCTCTC others(43): Show |
T | 14 | a0001c0001t0001g0078a0001c0001t0001g0086a0001c0001t0002g0095others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-23775_553-2372 others(54): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117384 | |||||
| chr10:113117386
|
TCTCTCTC others(41): Show |
T | 12 | a0001c0001t0001g0125a0001c0001t0002g0012a0001c0001t0002g0107others(9): Show | 12 | HG01099.hp1 HG01109.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-23773_553-2372 others(52): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117386 | |||||
| chr10:113117388
|
TCTCTCTC others(39): Show |
T | 8 | a0001c0001t0001g0031a0001c0001t0001g0042a0001c0001t0002g0096others(5): Show | 8 | HG00741.hp1 HG01106.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-23771_553-2372 others(50): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117388 | |||||
| chr10:113117390
|
TCTCTCTC others(37): Show |
T | 6 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0062others(3): Show | 6 | HG00642.hp2 HG00735.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-23769_553-2372 others(48): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117390 | |||||
| chr10:113117392
|
TCTCTCTC others(35): Show |
T | 5 | a0001c0001t0001g0044a0001c0001t0006g0005a0001c0001t0011g0176others(2): Show | 5 | HG01255.hp1 HG01433.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-23767_553-2372 others(46): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117392 | |||||
| chr10:113117394
|
T | C | 4 | a0001c0001t0004g0097a0001c0001t0009g0080a0001c0001t0024g0121others(1): Show | 4 | HG02922.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-23790T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117394 | ||||||
| chr10:113117394
|
TCTCTCTC others(33): Show |
T | 1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.553-23765_553-2372 others(44): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117394 | |||||
| chr10:113117395
|
CTCTCTCT others(18): Show |
C | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.553-23788_553-2376 others(29): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117395 | ||||||
| chr10:113117396
|
T | C | 20 | a0001c0001t0001g0058a0001c0001t0001g0074a0001c0001t0001g0101others(17): Show | 20 | HG00323.hp2 HG00738.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.553-23788T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117396 | ||||||
| chr10:113117396
|
TCTCTCTC others(31): Show |
T | 3 | a0001c0004t0008g0146a0001c0005t0019g0001a0001c0005t0019g0002 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.553-23763_553-2372 others(42): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117396 | |||||
| chr10:113117397
|
CTCTCTCT others(4): Show |
C | 1 | a0002c0002t0001g0088 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.553-23786_553-2377 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117397 | ||||||
| chr10:113117397
|
CTCTCTCT others(20): Show |
C | 1 | a0001c0001t0022g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.553-23786_553-2376 others(31): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117397 | ||||||
| chr10:113117398
|
T | C | 29 | a0001c0001t0001g0036a0001c0001t0001g0056a0001c0001t0001g0066others(26): Show | 29 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.553-23786T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117398 | ||||||
| chr10:113117399
|
CTCTCTCT others(4): Show |
C | 1 | a0009c0007t0001g0025 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.553-23784_553-2377 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117399 | ||||||
| chr10:113117399
|
CTCTCTCT others(6): Show |
C | 1 | a0001c0001t0023g0027 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.553-23784_553-2377 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117399 | ||||||
| chr10:113117400
|
T | C | 9 | a0001c0001t0001g0082a0001c0001t0001g0099a0001c0001t0001g0190others(6): Show | 9 | HG02486.hp2 HG02572.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-23784T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117400 | ||||||
| chr10:113117400
|
T | TCTCTCTC others(4): Show |
1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.553-23783_553-2377 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117400 | |||||
| chr10:113117400
|
TCTCTCTC others(27): Show |
T | 2 | a0001c0004t0008g0144a0003c0003t0020g0135 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.553-23759_553-2372 others(38): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117400 | |||||
| chr10:113117402
|
T | C | 1 | a0001c0001t0006g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.553-23782T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117402 | ||||||
| chr10:113117402
|
TCTCTCTC others(25): Show |
T | 8 | a0001c0001t0002g0102a0001c0001t0004g0097a0001c0001t0008g0092others(5): Show | 8 | HG00738.hp2 HG02145.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.553-23757_553-2372 others(36): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117402 | |||||
| chr10:113117404
|
TCTCTCTC others(23): Show |
T | 6 | a0001c0001t0001g0101a0001c0001t0004g0016a0001c0001t0005g0054others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-23755_553-2372 others(34): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117404 | |||||
| chr10:113117406
|
TCTCTCTC others(21): Show |
T | 12 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0130others(9): Show | 12 | HG00323.hp2 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-23753_553-2372 others(32): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117406 | |||||
| chr10:113117408
|
TCTCTCTC others(19): Show |
T | 10 | a0001c0001t0001g0066a0001c0001t0001g0131a0001c0001t0002g0118others(7): Show | 10 | HG00642.hp1 HG01081.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.553-23751_553-2372 others(30): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117408 | |||||
| chr10:113117410
|
TCTCTCTC others(17): Show |
T | 4 | a0001c0001t0003g0186a0001c0001t0006g0013a0001c0001t0010g0185others(1): Show | 4 | HG01346.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-23750_553-2372 others(28): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117410 | |||||
| chr10:113117411
|
CTCTCTCT others(8): Show |
C | 1 | a0002c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.553-23772_553-2375 others(19): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117411 | ||||||
| chr10:113117412
|
TCTCTCTC others(15): Show |
T | 4 | a0001c0001t0001g0058a0001c0001t0002g0006a0001c0001t0028g0014others(1): Show | 4 | HG02055.hp1 HG02886.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-23750_553-2372 others(26): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117412 | |||||
| chr10:113117414
|
TCTCTCTC others(13): Show |
T | 1 | a0001c0001t0006g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.553-23750_553-2373 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117414 | |||||
| chr10:113117416
|
T | C | 2 | a0001c0001t0001g0019a0005c0010t0003g0167 | 2 | HG00408.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.553-23768T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117416 | ||||||
| chr10:113117416
|
TCTCTCTC others(11): Show |
T | 1 | a0001c0001t0010g0111 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.553-23750_553-2373 others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117416 | |||||
| chr10:113117417
|
CTCTCTCT others(6): Show |
C | 1 | a0004c0006t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.553-23766_553-2375 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117417 | ||||||
| chr10:113117418
|
T | C | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.553-23766T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117418 | ||||||
| chr10:113117418
|
TCTCTCTC others(9): Show |
T | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.553-23750_553-2373 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117418 | |||||
| chr10:113117420
|
T | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0009g0081others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-23764T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117420 | ||||||
| chr10:113117420
|
TCTCTCTC others(7): Show |
T | 5 | a0001c0001t0001g0056a0001c0001t0001g0089a0001c0001t0001g0195others(2): Show | 5 | HG00438.hp1 HG00438.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-23750_553-2373 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117420 | |||||
| chr10:113117422
|
T | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG01496.hp1 HG01943.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-23762T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117422 | ||||||
| chr10:113117422
|
TCTCTCTC others(5): Show |
T | 11 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0191others(8): Show | 11 | HG00408.hp2 HG00597.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.553-23750_553-2373 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117422 | |||||
| chr10:113117424
|
T | C | 4 | a0001c0001t0002g0115a0001c0001t0003g0172a0001c0001t0037g0160others(1): Show | 4 | HG00140.hp1 HG01258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-23760T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117424 | ||||||
| chr10:113117424
|
TCTCTCTC others(3): Show |
T | 6 | a0001c0001t0001g0079a0001c0001t0002g0113a0001c0001t0003g0182others(3): Show | 6 | HG00735.hp1 HG00741.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.553-23750_553-2374 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117424 | |||||
| chr10:113117426
|
T | C | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0002g0173others(4): Show | 7 | HG01258.hp2 HG01981.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.553-23758T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117426 | ||||||
| chr10:113117426
|
TCTCTCTC others(1): Show |
T | 7 | a0001c0001t0001g0051a0001c0001t0001g0063a0001c0001t0001g0190others(4): Show | 7 | HG00099.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-23750_553-2374 others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117426 | |||||
| chr10:113117428
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0012g0178a0001c0001t0016g0023 | 3 | HG00280.hp2 HG02165.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.553-23756T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117428 | ||||||
| chr10:113117428
|
T | TCTCC | 2 | a0001c0001t0001g0059a0001c0001t0001g0123 | 2 | HG00408.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.553-23753_553-2375 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117428 | |||||
| chr10:113117428
|
TCTCTCC | T | 7 | a0001c0001t0001g0034a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG01496.hp1 HG01943.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-23750_553-2374 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117428 | |||||
| chr10:113117430
|
TCTCC | T | 6 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0068others(3): Show | 6 | HG00140.hp1 HG01258.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-23750_553-2374 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117430 | |||||
| chr10:113117432
|
TCC | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0006g0149others(4): Show | 7 | HG01258.hp2 HG02040.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-23750_553-2374 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117432 | |||||
| chr10:113117434
|
C | CCTCTCT | 3 | a0001c0001t0002g0117a0001c0001t0031g0010a0004c0006t0001g0053 | 3 | HG01515.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.553-23731_553-2372 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117434 | |||||
| chr10:113117434
|
C | T | 35 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0040others(32): Show | 35 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.553-23750C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117434 | ||||||
| chr10:113117457
|
C | T | 4 | a0001c0001t0001g0099a0001c0001t0004g0132a0001c0001t0028g0014others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-23727C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117457 | ||||||
| chr10:113117459
|
T | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0196 | 2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.553-23725T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117459 | ||||||
| chr10:113117470
|
C | A | 8 | a0001c0001t0001g0101a0001c0001t0004g0016a0001c0001t0004g0076others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.553-23714C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117470 | ||||||
| chr10:113117744
|
GAAGAA | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0193a0001c0001t0001g0196others(10): Show | 13 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.553-23435_553-2343 others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113117744 | |||||
| chr10:113117804
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0002g0155a0001c0004t0013g0145 | 3 | HG02818.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.553-23380A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117804 | ||||||
| chr10:113117964
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-23220C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117964 | ||||||
| chr10:113117973
|
C | T | 1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.553-23211C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117973 | ||||||
| chr10:113117996
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0115 | 2 | HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.553-23188A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113117996 | ||||||
| chr10:113118100
|
A | G | 2 | a0001c0001t0010g0098a0003c0003t0011g0009 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.553-23084A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118100 | ||||||
| chr10:113118108
|
G | T | 11 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0004g0016others(8): Show | 11 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.553-23076G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118108 | ||||||
| chr10:113118482
|
T | A | 3 | a0001c0001t0006g0188a0001c0001t0008g0148a0001c0001t0010g0127 | 3 | HG01243.hp2 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.553-22702T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118482 | ||||||
| chr10:113118515
|
TGG | T | 9 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0004g0132others(6): Show | 9 | HG01243.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.553-22664_553-2266 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118515 | |||||
| chr10:113118518
|
G | GGTGT | 25 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0051others(22): Show | 25 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.553-22665_553-2266 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GGTGTGT | 13 | a0001c0001t0001g0130a0001c0001t0006g0013a0001c0001t0008g0092others(10): Show | 13 | HG01081.hp1 HG01109.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.553-22665_553-2266 others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GGTGTGTG others(3): Show |
26 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0040others(23): Show | 26 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.553-22665_553-2266 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GGTGTGTG others(5): Show |
37 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(34): Show | 37 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.553-22665_553-2266 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GGTGTGTG others(7): Show |
20 | a0001c0001t0001g0038a0001c0001t0001g0087a0001c0001t0001g0197others(17): Show | 20 | HG00597.hp1 HG01099.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.553-22665_553-2266 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GGTGTGTG others(9): Show |
7 | a0001c0001t0001g0068a0001c0001t0002g0113a0001c0001t0003g0163others(4): Show | 7 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-22665_553-2266 others(20): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GGTGTGTG others(13): Show |
1 | a0001c0001t0002g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.553-22665_553-2266 others(24): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GGTGTGTG others(15): Show |
1 | a0002c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.553-22665_553-2266 others(26): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
G | GTGTGTGT others(4): Show |
1 | a0001c0004t0013g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.553-22666_553-2266 others(15): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118518 | ||||||
| chr10:113118518
|
G | GTGTGTGT others(6): Show |
1 | a0002c0002t0003g0171 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.553-22666_553-2266 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118518 | ||||||
| chr10:113118518
|
GGGGTGTG others(3): Show |
G | 3 | a0001c0001t0007g0032a0001c0001t0016g0024a0002c0002t0001g0088 | 3 | HG00597.hp2 HG02165.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.553-22664_553-2265 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118518
|
GGGGTGTG others(7): Show |
G | 1 | a0001c0001t0012g0169 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.553-22664_553-2265 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118518 | |||||
| chr10:113118520
|
G | GGTGT | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0003g0172others(2): Show | 5 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-22633_553-2263 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118520 | |||||
| chr10:113118520
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0044 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.553-22639_553-2263 others(14): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118520 | |||||
| chr10:113118520
|
G | GGTGTGTG others(5): Show |
1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-22641_553-2263 others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118520 | |||||
| chr10:113118520
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0191 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.553-22643_553-2263 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118520 | |||||
| chr10:113118520
|
G | T | 147 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.553-22664G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118520 | ||||||
| chr10:113118520
|
GGT | G | 20 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0074others(17): Show | 20 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.553-22631_553-2263 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118520 | |||||
| chr10:113118520
|
GGTGT | G | 5 | a0001c0001t0002g0118a0001c0001t0003g0186a0001c0001t0005g0067others(2): Show | 5 | HG00642.hp1 HG01123.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-22633_553-2263 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118520 | |||||
| chr10:113118554
|
T | TGTGTGTG others(6): Show |
1 | a0001c0001t0002g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.553-22630_553-2262 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118554 | ||||||
| chr10:113118613
|
T | C | 3 | a0001c0001t0005g0033a0001c0001t0005g0064a0001c0001t0007g0189 | 3 | HG03942.hp1 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.553-22571T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118613 | ||||||
| chr10:113118643
|
GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.553-22521_553-2249 others(28): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118643 | |||||
| chr10:113118644
|
T | G | 1 | a0001c0001t0045g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.553-22540T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118644 | ||||||
| chr10:113118654
|
GT | G | 33 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(30): Show | 33 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.553-22521delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118654 | |||||
| chr10:113118654
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0013g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.553-22520_553-2250 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118654 | |||||
| chr10:113118654
|
GTTTTTTT others(7): Show |
G | 5 | a0001c0001t0006g0188a0001c0001t0008g0148a0001c0001t0010g0127others(2): Show | 5 | HG01243.hp2 HG02165.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-22511_553-2249 others(18): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118654 | |||||
| chr10:113118654
|
GTTTTTTT others(8): Show |
G | 65 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0062others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.553-22521_553-2250 others(19): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118654 | |||||
| chr10:113118663
|
T | C | 1 | a0001c0011t0035g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.553-22521T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118663 | ||||||
| chr10:113118664
|
GT | G | 22 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(19): Show | 22 | HG00408.hp2 HG01099.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.553-22507delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118664 | |||||
| chr10:113118664
|
GTTT | G | 49 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0056others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.553-22509_553-2250 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118664 | |||||
| chr10:113118665
|
TTTTTTTT others(6): Show |
T | 33 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(30): Show | 33 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.553-22510_553-2249 others(17): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113118665 | |||||
| chr10:113118667
|
T | G | 3 | a0001c0001t0001g0129a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.553-22517T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118667 | ||||||
| chr10:113118677
|
T | G | 1 | a0002c0002t0007g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.553-22507T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118677 | ||||||
| chr10:113118678
|
G | T | 1 | a0002c0002t0007g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.553-22506G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118678 | ||||||
| chr10:113118686
|
T | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0158 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.553-22498T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118686 | ||||||
| chr10:113118979
|
G | A | 2 | a0002c0002t0018g0022a0005c0010t0003g0167 | 2 | HG02040.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.553-22205G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113118979 | ||||||
| chr10:113119020
|
G | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0193a0001c0001t0001g0196others(7): Show | 10 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.553-22164G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119020 | ||||||
| chr10:113119059
|
A | G | 7 | a0001c0001t0001g0101a0001c0001t0004g0016a0001c0001t0005g0054others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-22125A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119059 | ||||||
| chr10:113119161
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.553-22023C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119161 | ||||||
| chr10:113119497
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.553-21687G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119497 | ||||||
| chr10:113119670
|
G | GT | 56 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0056others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.553-21503dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113119670 | |||||
| chr10:113119670
|
GT | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0193a0001c0001t0001g0196others(8): Show | 11 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(8): Show |
intron_variant | MODIFIER | c.553-21503delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113119670 | |||||
| chr10:113119680
|
T | A | 1 | a0001c0001t0002g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.553-21504T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119680 | ||||||
| chr10:113119680
|
T | TA | 30 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 30 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-21504_553-2150 others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119680 | ||||||
| chr10:113119681
|
T | A | 32 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(29): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.553-21503T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119681 | ||||||
| chr10:113119682
|
A | T | 19 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0002g0006others(16): Show | 19 | HG01081.hp1 HG01243.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.553-21502A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119682 | ||||||
| chr10:113119827
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.553-21357C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119827 | ||||||
| chr10:113119965
|
C | T | 1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.553-21219C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113119965 | ||||||
| chr10:113120470
|
G | A | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.553-20714G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113120470 | ||||||
| chr10:113120583
|
T | C | 31 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(28): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.553-20601T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113120583 | ||||||
| chr10:113120753
|
T | C | 1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.553-20431T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113120753 | ||||||
| chr10:113120792
|
A | T | 94 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0041others(91): Show | 94 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.553-20392A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113120792 | ||||||
| chr10:113121669
|
C | T | 30 | a0001c0001t0001g0062a0001c0001t0001g0101a0001c0001t0001g0125others(27): Show | 30 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-19515C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121669 | ||||||
| chr10:113121728
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.553-19456G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121728 | ||||||
| chr10:113121742
|
AAC | A | 18 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0002g0142others(15): Show | 18 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.553-19431_553-1943 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113121742 | |||||
| chr10:113121742
|
AACACACA others(28): Show |
A | 2 | a0001c0001t0001g0062a0001c0004t0013g0145 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.553-19429_553-1939 others(39): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113121742 | |||||
| chr10:113121754
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.553-19430C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121754 | ||||||
| chr10:113121768
|
T | C | 2 | a0001c0001t0010g0098a0003c0003t0011g0009 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.553-19416T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121768 | ||||||
| chr10:113121775
|
A | AAC | 61 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0001g0044others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.553-19389_553-1938 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113121775 | |||||
| chr10:113121775
|
A | AACAC | 5 | a0001c0001t0002g0006a0001c0001t0006g0136a0001c0005t0006g0138others(2): Show | 5 | HG02886.hp1 HG04228.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-19391_553-1938 others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113121775 | |||||
| chr10:113121775
|
AAC | A | 2 | a0001c0001t0013g0103a0001c0001t0014g0055 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.553-19389_553-1938 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113121775 | |||||
| chr10:113121791
|
C | T | 2 | a0001c0005t0019g0001a0001c0005t0019g0002 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.553-19393C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121791 | ||||||
| chr10:113121899
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.553-19285C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121899 | ||||||
| chr10:113121952
|
C | T | 2 | a0001c0001t0006g0140a0007c0008t0002g0015 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.553-19232C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121952 | ||||||
| chr10:113121978
|
C | T | 38 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0066others(35): Show | 38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.553-19206C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121978 | ||||||
| chr10:113121994
|
G | A | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.553-19190G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113121994 | ||||||
| chr10:113122089
|
C | G | 2 | a0001c0001t0046g0152a0001c0001t0047g0150 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.553-19095C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113122089 | ||||||
| chr10:113122771
|
A | G | 30 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 30 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-18413A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113122771 | ||||||
| chr10:113122912
|
A | G | 21 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0001g0130others(18): Show | 21 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.553-18272A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113122912 | ||||||
| chr10:113123278
|
C | T | 1 | a0002c0002t0003g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.553-17906C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113123278 | ||||||
| chr10:113123497
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.553-17687C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113123497 | ||||||
| chr10:113123563
|
G | A | 71 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0066others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.553-17621G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113123563 | ||||||
| chr10:113123565
|
T | C | 2 | a0001c0001t0010g0098a0003c0003t0011g0009 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.553-17619T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113123565 | ||||||
| chr10:113123586
|
A | C | 2 | a0001c0001t0010g0098a0003c0003t0011g0009 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.553-17598A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113123586 | ||||||
| chr10:113124193
|
TA | T | 103 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0041others(100): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.553-16983delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113124193 | |||||
| chr10:113124201
|
AT | A | 49 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0056others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.553-16975delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113124201 | |||||
| chr10:113124556
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0003g0172 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.553-16628G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113124556 | ||||||
| chr10:113124582
|
A | G | 3 | a0001c0001t0001g0129a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.553-16602A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113124582 | ||||||
| chr10:113124899
|
C | T | 2 | a0001c0001t0001g0062a0001c0004t0013g0145 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.553-16285C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113124899 | ||||||
| chr10:113124981
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.553-16203T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113124981 | ||||||
| chr10:113124982
|
G | T | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.553-16202G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113124982 | ||||||
| chr10:113124983
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.553-16201T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113124983 | ||||||
| chr10:113125154
|
C | T | 1 | a0001c0001t0006g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.553-16030C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113125154 | ||||||
| chr10:113125208
|
G | A | 71 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0066others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.553-15976G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113125208 | ||||||
| chr10:113125243
|
GA | G | 89 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.553-15929delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113125243 | |||||
| chr10:113125323
|
A | AT | 23 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0001g0130others(20): Show | 23 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.553-15852dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113125323 | |||||
| chr10:113125458
|
C | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.553-15726C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113125458 | ||||||
| chr10:113125482
|
G | GT | 7 | a0001c0001t0001g0036a0001c0001t0001g0082a0001c0001t0001g0087others(4): Show | 7 | HG00597.hp2 HG02132.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.553-15696dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113125482 | |||||
| chr10:113125595
|
G | A | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-15589G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113125595 | ||||||
| chr10:113125795
|
AAG | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0074others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.553-15385_553-1538 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113125795 | |||||
| chr10:113126038
|
C | T | 9 | a0001c0001t0001g0130a0001c0001t0006g0013a0001c0001t0008g0092others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.553-15146C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126038 | ||||||
| chr10:113126107
|
G | GT | 3 | a0001c0001t0002g0155a0001c0001t0013g0103a0001c0001t0014g0055 | 3 | HG02280.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.553-15073dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113126107 | |||||
| chr10:113126111
|
TG | T | 35 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0079others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.553-15072delG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126111 | ||||||
| chr10:113126112
|
G | T | 143 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(140): Show | 143 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.553-15072G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126112 | ||||||
| chr10:113126175
|
A | G | 3 | a0001c0001t0001g0191a0001c0001t0001g0195a0002c0002t0001g0200 | 3 | HG00438.hp1 HG00597.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.553-15009A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126175 | ||||||
| chr10:113126214
|
C | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0074others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.553-14970C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126214 | ||||||
| chr10:113126317
|
C | T | 1 | a0002c0002t0005g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.553-14867C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126317 | ||||||
| chr10:113126441
|
G | A | 2 | a0001c0001t0001g0062a0001c0004t0013g0145 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.553-14743G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126441 | ||||||
| chr10:113126562
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.553-14622C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126562 | ||||||
| chr10:113126752
|
C | T | 5 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG00642.hp2 HG01099.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-14432C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113126752 | ||||||
| chr10:113127219
|
G | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-13965G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127219 | ||||||
| chr10:113127243
|
GT | G | 131 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(128): Show | 131 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.553-13927delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127243 | |||||
| chr10:113127243
|
GTT | G | 5 | a0001c0001t0002g0142a0001c0001t0002g0173a0001c0001t0006g0188others(2): Show | 5 | HG01243.hp2 HG01981.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.553-13928_553-1392 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127243 | |||||
| chr10:113127299
|
C | T | 1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.553-13885C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127299 | ||||||
| chr10:113127429
|
G | C | 145 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.553-13755G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127429 | ||||||
| chr10:113127459
|
A | G | 145 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(142): Show | 145 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.553-13725A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127459 | ||||||
| chr10:113127554
|
TTTG | T | 22 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0001g0130others(19): Show | 22 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.553-13618_553-1361 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127554 | |||||
| chr10:113127800
|
A | C | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-13384A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127800 | ||||||
| chr10:113127811
|
A | T | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.553-13373A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127811 | ||||||
| chr10:113127866
|
C | CT | 45 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0068others(42): Show | 45 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.553-13297dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127866 | |||||
| chr10:113127866
|
C | CTT | 5 | a0001c0001t0001g0196a0001c0001t0005g0054a0001c0001t0014g0153others(2): Show | 5 | HG01175.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-13298_553-1329 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127866 | |||||
| chr10:113127866
|
CT | C | 51 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.553-13297delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127866 | |||||
| chr10:113127866
|
CTT | C | 23 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0041others(20): Show | 23 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.553-13298_553-1329 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127866 | |||||
| chr10:113127866
|
CTTT | C | 15 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0002g0142others(12): Show | 15 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.553-13299_553-1329 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113127866 | |||||
| chr10:113127922
|
A | G | 33 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0074others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.553-13262A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127922 | ||||||
| chr10:113127963
|
T | C | 30 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 30 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-13221T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113127963 | ||||||
| chr10:113128058
|
A | G | 27 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(24): Show | 27 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.553-13126A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113128058 | ||||||
| chr10:113128417
|
TA | T | 3 | a0001c0001t0001g0062a0001c0001t0002g0155a0001c0004t0013g0145 | 3 | HG02818.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.553-12764delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113128417 | |||||
| chr10:113128438
|
C | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-12746C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113128438 | ||||||
| chr10:113128848
|
C | T | 2 | a0001c0001t0013g0103a0001c0001t0014g0055 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.553-12336C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113128848 | ||||||
| chr10:113128849
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0066others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.553-12335G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113128849 | ||||||
| chr10:113128889
|
G | T | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.553-12295G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113128889 | ||||||
| chr10:113128969
|
G | C | 129 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(126): Show | 129 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.553-12215G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113128969 | ||||||
| chr10:113128982
|
A | G | 1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.553-12202A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113128982 | ||||||
| chr10:113129012
|
G | A | 27 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(24): Show | 27 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.553-12172G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113129012 | ||||||
| chr10:113129068
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.553-12116G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113129068 | ||||||
| chr10:113129206
|
C | T | 1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.553-11978C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113129206 | ||||||
| chr10:113129502
|
T | A | 28 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(25): Show | 28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.553-11682T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113129502 | ||||||
| chr10:113129658
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.553-11526C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113129658 | ||||||
| chr10:113130037
|
G | A | 1 | a0002c0002t0005g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.553-11147G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130037 | ||||||
| chr10:113130078
|
TC | T | 124 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(121): Show | 124 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.553-11098delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113130078 | |||||
| chr10:113130141
|
G | T | 33 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0074others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.553-11043G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130141 | ||||||
| chr10:113130142
|
C | A | 33 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0074others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.553-11042C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130142 | ||||||
| chr10:113130180
|
T | A | 3 | a0001c0001t0001g0062a0001c0001t0002g0155a0001c0004t0013g0145 | 3 | HG02818.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.553-11004T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130180 | ||||||
| chr10:113130351
|
T | C | 2 | a0001c0001t0013g0103a0001c0001t0014g0055 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.553-10833T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130351 | ||||||
| chr10:113130752
|
A | AATT | 44 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(41): Show | 44 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.553-10407_553-1040 others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113130752 | |||||
| chr10:113130859
|
G | A | 1 | a0001c0001t0006g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.553-10325G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130859 | ||||||
| chr10:113130913
|
C | T | 3 | a0001c0001t0003g0186a0001c0001t0005g0067a0001c0001t0044g0070 | 3 | HG01123.hp2 HG01175.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.553-10271C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130913 | ||||||
| chr10:113130915
|
G | A | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-10269G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113130915 | ||||||
| chr10:113131065
|
C | T | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.553-10119C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131065 | ||||||
| chr10:113131150
|
G | A | 6 | a0001c0001t0001g0101a0001c0001t0004g0016a0001c0001t0005g0054others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-10034G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131150 | ||||||
| chr10:113131200
|
C | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-9984C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131200 | ||||||
| chr10:113131264
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0011g0175a0001c0001t0011g0184 | 3 | HG01081.hp1 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.553-9920A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131264 | ||||||
| chr10:113131382
|
G | C | 1 | a0002c0002t0003g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.553-9802G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131382 | ||||||
| chr10:113131673
|
G | C | 27 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(24): Show | 27 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.553-9511G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131673 | ||||||
| chr10:113131684
|
G | A | 3 | a0001c0001t0002g0102a0001c0001t0005g0122a0001c0001t0022g0050 | 3 | HG00738.hp2 HG01123.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.553-9500G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131684 | ||||||
| chr10:113131697
|
A | G | 28 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(25): Show | 28 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.553-9487A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131697 | ||||||
| chr10:113131839
|
A | C | 1 | a0001c0001t0022g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.553-9345A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131839 | ||||||
| chr10:113131846
|
G | A | 2 | a0001c0001t0012g0165a0002c0002t0005g0043 | 2 | HG01081.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.553-9338G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131846 | ||||||
| chr10:113131870
|
T | C | 4 | a0001c0001t0001g0099a0001c0001t0004g0132a0001c0001t0028g0014others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-9314T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113131870 | ||||||
| chr10:113132077
|
C | T | 1 | a0001c0001t0016g0024 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.553-9107C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132077 | ||||||
| chr10:113132308
|
C | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0012g0178others(1): Show | 4 | HG00280.hp2 HG01070.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-8876C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132308 | ||||||
| chr10:113132332
|
G | A | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.553-8852G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132332 | ||||||
| chr10:113132520
|
T | A | 2 | a0001c0001t0006g0140a0007c0008t0002g0015 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.553-8664T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132520 | ||||||
| chr10:113132521
|
T | A | 2 | a0001c0001t0006g0140a0007c0008t0002g0015 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.553-8663T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132521 | ||||||
| chr10:113132709
|
T | C | 148 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.553-8475T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132709 | ||||||
| chr10:113132845
|
A | G | 1 | a0001c0001t0038g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.553-8339A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132845 | ||||||
| chr10:113132883
|
C | T | 3 | a0001c0001t0006g0188a0001c0001t0008g0148a0001c0001t0010g0127 | 3 | HG01243.hp2 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.553-8301C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113132883 | ||||||
| chr10:113133069
|
T | C | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-8115T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113133069 | ||||||
| chr10:113133327
|
C | T | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.553-7857C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113133327 | ||||||
| chr10:113133730
|
C | T | 11 | a0001c0001t0001g0129a0001c0001t0006g0005a0001c0001t0006g0140others(8): Show | 11 | HG01081.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.553-7454C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113133730 | ||||||
| chr10:113133750
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.553-7434C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113133750 | ||||||
| chr10:113133923
|
G | T | 61 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(58): Show | 61 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.553-7261G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113133923 | ||||||
| chr10:113133949
|
C | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-7235C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113133949 | ||||||
| chr10:113134194
|
A | C | 83 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(80): Show | 83 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.553-6990A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134194 | ||||||
| chr10:113134197
|
C | G | 83 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(80): Show | 83 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.553-6987C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134197 | ||||||
| chr10:113134223
|
A | G | 1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.553-6961A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134223 | ||||||
| chr10:113134237
|
C | CCTCTCTG | 4 | a0001c0001t0003g0179a0001c0001t0036g0116a0002c0002t0001g0192others(1): Show | 4 | HG01256.hp2 HG03831.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-6947_553-6946i others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134237 | ||||||
| chr10:113134240
|
GGTA | G | 4 | a0001c0001t0003g0179a0001c0001t0036g0116a0002c0002t0001g0192others(1): Show | 4 | HG01256.hp2 HG03831.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-6943_553-6941d others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134240 | ||||||
| chr10:113134243
|
A | G | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.553-6941A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134243 | ||||||
| chr10:113134262
|
C | T | 1 | a0001c0001t0003g0186 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.553-6922C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134262 | ||||||
| chr10:113134528
|
G | A | 1 | a0001c0001t0031g0010 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.553-6656G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134528 | ||||||
| chr10:113134577
|
C | A | 1 | a0001c0001t0012g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.553-6607C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134577 | ||||||
| chr10:113134594
|
G | A | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-6590G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134594 | ||||||
| chr10:113134662
|
C | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-6522C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134662 | ||||||
| chr10:113134727
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.553-6457C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134727 | ||||||
| chr10:113134745
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.553-6439C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134745 | ||||||
| chr10:113134820
|
C | G | 2 | a0001c0001t0013g0103a0001c0001t0014g0055 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.553-6364C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113134820 | ||||||
| chr10:113135034
|
G | A | 1 | a0001c0001t0006g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.553-6150G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113135034 | ||||||
| chr10:113135536
|
T | C | 95 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(92): Show | 95 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.553-5648T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113135536 | ||||||
| chr10:113135565
|
G | A | 1 | a0001c0004t0008g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.553-5619G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113135565 | ||||||
| chr10:113135613
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.553-5571C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113135613 | ||||||
| chr10:113135729
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.553-5455A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113135729 | ||||||
| chr10:113135825
|
G | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-5359G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113135825 | ||||||
| chr10:113136152
|
C | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-5032C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113136152 | ||||||
| chr10:113136252
|
G | A | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.553-4932G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113136252 | ||||||
| chr10:113136334
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.553-4850G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113136334 | ||||||
| chr10:113136941
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.553-4243C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113136941 | ||||||
| chr10:113137032
|
T | C | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.553-4152T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137032 | ||||||
| chr10:113137062
|
T | A | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-4122T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137062 | ||||||
| chr10:113137382
|
A | G | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-3802A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137382 | ||||||
| chr10:113137461
|
A | C | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-3723A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137461 | ||||||
| chr10:113137599
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0196 | 2 | NA19007.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.553-3585A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137599 | ||||||
| chr10:113137804
|
G | A | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.553-3380G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137804 | ||||||
| chr10:113137890
|
G | A | 27 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(24): Show | 27 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.553-3294G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137890 | ||||||
| chr10:113137914
|
G | C | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-3270G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113137914 | ||||||
| chr10:113138034
|
G | C | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.553-3150G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138034 | ||||||
| chr10:113138248
|
C | T | 2 | a0001c0001t0006g0140a0007c0008t0002g0015 | 2 | HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.553-2936C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138248 | ||||||
| chr10:113138334
|
T | C | 146 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.553-2850T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138334 | ||||||
| chr10:113138463
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0002g0158 | 2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.553-2721G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138463 | ||||||
| chr10:113138638
|
A | G | 4 | a0001c0001t0002g0006a0001c0001t0004g0076a0001c0001t0006g0136others(1): Show | 4 | HG02647.hp1 HG02886.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.553-2546A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138638 | ||||||
| chr10:113138758
|
T | G | 1 | a0001c0001t0012g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.553-2426T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138758 | ||||||
| chr10:113138763
|
G | A | 33 | a0001c0001t0001g0036a0001c0001t0001g0044a0001c0001t0001g0056others(30): Show | 33 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.553-2421G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138763 | ||||||
| chr10:113138893
|
A | C | 1 | a0001c0001t0005g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.553-2291A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138893 | ||||||
| chr10:113138980
|
T | C | 107 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(104): Show | 107 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.553-2204T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113138980 | ||||||
| chr10:113139022
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.553-2162C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139022 | ||||||
| chr10:113139155
|
A | C | 27 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(24): Show | 27 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.553-2029A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139155 | ||||||
| chr10:113139175
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.553-2009T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139175 | ||||||
| chr10:113139250
|
G | A | 1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.553-1934G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139250 | ||||||
| chr10:113139356
|
A | T | 107 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(104): Show | 107 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.553-1828A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139356 | ||||||
| chr10:113139358
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.553-1826C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139358 | ||||||
| chr10:113139433
|
G | C | 1 | a0001c0001t0042g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.553-1751G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139433 | ||||||
| chr10:113139594
|
AAG | A | 107 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(104): Show | 107 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.553-1587_553-1586d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113139594 | |||||
| chr10:113139611
|
T | C | 1 | a0001c0001t0003g0172 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.553-1573T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139611 | ||||||
| chr10:113139641
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.553-1543G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139641 | ||||||
| chr10:113139674
|
C | T | 96 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(93): Show | 96 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.553-1510C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139674 | ||||||
| chr10:113139687
|
T | G | 107 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(104): Show | 107 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.553-1497T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113139687 | ||||||
| chr10:113139811
|
T | TA | 44 | a0001c0001t0001g0017a0001c0001t0001g0044a0001c0001t0001g0056others(41): Show | 44 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.553-1354dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113139811 | |||||
| chr10:113139811
|
T | TAA | 6 | a0001c0001t0001g0074a0001c0001t0003g0163a0001c0001t0004g0133others(3): Show | 6 | HG00140.hp2 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.553-1355_553-1354d others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113139811 | |||||
| chr10:113139811
|
TAAA | T | 105 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(102): Show | 105 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.553-1356_553-1354d others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 113139811 | |||||
| chr10:113140105
|
C | T | 1 | a0001c0001t0004g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.553-1079C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140105 | ||||||
| chr10:113140170
|
T | A | 1 | a0001c0001t0002g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.553-1014T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140170 | ||||||
| chr10:113140207
|
C | G | 182 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.553-977C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140207 | ||||||
| chr10:113140280
|
G | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0115 | 2 | HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.553-904G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140280 | ||||||
| chr10:113140510
|
T | G | 1 | a0003c0003t0011g0009 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.553-674T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140510 | ||||||
| chr10:113140658
|
C | T | 17 | a0001c0001t0001g0079a0001c0001t0001g0125a0001c0001t0001g0130others(14): Show | 17 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.553-526C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140658 | ||||||
| chr10:113140740
|
A | G | 57 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0062others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.553-444A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140740 | ||||||
| chr10:113140748
|
G | T | 1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.553-436G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140748 | ||||||
| chr10:113140765
|
T | C | 3 | a0001c0001t0011g0176a0001c0005t0019g0001a0001c0005t0019g0002 | 3 | HG02896.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.553-419T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140765 | ||||||
| chr10:113140800
|
A | C | 56 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0062others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.553-384A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140800 | ||||||
| chr10:113140836
|
T | C | 56 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0062others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.553-348T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140836 | ||||||
| chr10:113140868
|
T | C | 61 | a0001c0001t0001g0017a0001c0001t0001g0058a0001c0001t0001g0062others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.553-316T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 5/14 | chr10 | 113140868 | ||||||
| chr10:113141333
|
G | A | 2 | a0001c0001t0001g0029a0002c0002t0001g0021 | 2 | HG02132.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.685+17G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141333 | ||||||
| chr10:113141429
|
C | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.685+113C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141429 | ||||||
| chr10:113141430
|
G | A | 1 | a0001c0001t0006g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.685+114G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141430 | ||||||
| chr10:113141435
|
TG | T | 30 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 30 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.685+126delG | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr10 | 113141435 | |||||
| chr10:113141442
|
G | T | 30 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(27): Show | 30 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.685+126G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141442 | ||||||
| chr10:113141472
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.685+156G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141472 | ||||||
| chr10:113141786
|
A | G | 29 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0079others(26): Show | 29 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.685+470A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141786 | ||||||
| chr10:113141812
|
A | G | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.685+496A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141812 | ||||||
| chr10:113141816
|
A | G | 24 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(21): Show | 24 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.685+500A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113141816 | ||||||
| chr10:113142040
|
T | C | 1 | a0001c0001t0003g0179 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.685+724T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113142040 | ||||||
| chr10:113142114
|
C | T | 24 | a0001c0001t0001g0062a0001c0001t0001g0074a0001c0001t0001g0079others(21): Show | 24 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.685+798C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113142114 | ||||||
| chr10:113142270
|
A | G | 9 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0004g0126others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.685+954A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113142270 | ||||||
| chr10:113142374
|
C | T | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.685+1058C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113142374 | ||||||
| chr10:113142446
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.685+1130G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113142446 | ||||||
| chr10:113142852
|
T | C | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.686-1071T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113142852 | ||||||
| chr10:113142853
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.686-1070C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113142853 | ||||||
| chr10:113143052
|
C | G | 33 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(30): Show | 33 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.686-871C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143052 | ||||||
| chr10:113143155
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.686-768G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143155 | ||||||
| chr10:113143165
|
G | T | 1 | a0002c0002t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.686-758G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143165 | ||||||
| chr10:113143217
|
C | A | 1 | a0001c0001t0011g0176 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.686-706C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143217 | ||||||
| chr10:113143231
|
C | T | 8 | a0001c0001t0001g0089a0001c0001t0001g0191a0001c0001t0010g0111others(5): Show | 8 | HG00438.hp2 HG00597.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.686-692C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143231 | ||||||
| chr10:113143235
|
G | T | 2 | a0001c0001t0031g0010a0004c0006t0001g0053 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.686-688G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143235 | ||||||
| chr10:113143368
|
G | C | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.686-555G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143368 | ||||||
| chr10:113143548
|
G | A | 1 | a0005c0010t0003g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.686-375G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143548 | ||||||
| chr10:113143826
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.686-97G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 6/14 | chr10 | 113143826 | ||||||
| chr10:113144071
|
C | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0158a0001c0001t0004g0016 | 3 | HG01884.hp1 HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.788+46C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144071 | ||||||
| chr10:113144088
|
C | CTGTGTGT others(3): Show |
2 | a0001c0004t0008g0144a0001c0004t0008g0146 | 2 | HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.788+65_788+74dupGT others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144088 | |||||
| chr10:113144088
|
C | CTGTGTGT others(7): Show |
1 | a0001c0004t0013g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.788+74_788+75insGT others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144088 | |||||
| chr10:113144088
|
CTGTGTGT others(17): Show |
C | 24 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(21): Show | 24 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.788+75_788+98delCT others(22): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144088 | |||||
| chr10:113144100
|
C | CTG | 9 | a0001c0001t0003g0163a0001c0001t0004g0076a0001c0001t0005g0122others(6): Show | 9 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.788+111_788+112dup others(2): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
C | CTGTG | 2 | a0001c0001t0002g0006a0001c0005t0006g0138 | 2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.788+109_788+112dup others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
C | CTGTGTGT others(1): Show |
2 | a0001c0001t0001g0099a0001c0001t0002g0094 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.788+105_788+112dup others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
C | CTGTGTGT others(3): Show |
7 | a0001c0001t0004g0126a0001c0001t0004g0132a0001c0001t0004g0141others(4): Show | 7 | HG02257.hp1 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.788+103_788+112dup others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0004g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.788+101_788+112dup others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
C | G | 4 | a0001c0001t0008g0139a0001c0004t0008g0144a0001c0004t0008g0146others(1): Show | 4 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.788+75C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144100 | ||||||
| chr10:113144100
|
CTG | C | 13 | a0001c0001t0001g0049a0001c0001t0002g0102a0001c0001t0002g0104others(10): Show | 13 | HG00099.hp2 HG00323.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.788+111_788+112del others(2): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
CTGTG | C | 52 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0044others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.788+109_788+112del others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
CTGTGTG | C | 4 | a0001c0001t0001g0191a0001c0001t0009g0045a0002c0002t0001g0200others(1): Show | 4 | HG00280.hp1 HG00597.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.788+107_788+112del others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
CTGTGTGT others(1): Show |
C | 14 | a0001c0001t0001g0193a0001c0001t0002g0158a0001c0001t0005g0033others(11): Show | 14 | HG01496.hp2 HG02280.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.788+105_788+112del others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
CTGTGTGT others(3): Show |
C | 32 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(29): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.788+103_788+112del others(10): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0043g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.788+101_788+112del others(12): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144100
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0007g0032 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.788+99_788+112delG others(13): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144100 | |||||
| chr10:113144108
|
G | C | 2 | a0001c0001t0011g0175a0001c0001t0011g0184 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.788+83G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144108 | ||||||
| chr10:113144110
|
G | C | 1 | a0001c0001t0006g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.788+85G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144110 | ||||||
| chr10:113144132
|
GTGTGTA | G | 3 | a0001c0001t0004g0097a0001c0001t0024g0121a0003c0003t0021g0120 | 3 | HG02922.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.788+113_788+118del others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144132 | |||||
| chr10:113144134
|
GTGTA | G | 2 | a0001c0001t0011g0175a0001c0001t0011g0184 | 2 | HG01081.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.788+113_788+116del others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113144134 | |||||
| chr10:113144217
|
G | A | 1 | a0003c0003t0021g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.788+192G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144217 | ||||||
| chr10:113144262
|
C | T | 1 | a0001c0001t0006g0005 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.788+237C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144262 | ||||||
| chr10:113144277
|
G | A | 42 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0049others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.788+252G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144277 | ||||||
| chr10:113144369
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.788+344G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144369 | ||||||
| chr10:113144442
|
T | G | 22 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0034others(19): Show | 22 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.788+417T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144442 | ||||||
| chr10:113144485
|
C | T | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.788+460C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144485 | ||||||
| chr10:113144651
|
G | A | 31 | a0001c0001t0001g0031a0001c0001t0001g0041a0001c0001t0001g0042others(28): Show | 31 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.788+626G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144651 | ||||||
| chr10:113144729
|
G | A | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.788+704G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144729 | ||||||
| chr10:113144775
|
A | T | 180 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.788+750A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144775 | ||||||
| chr10:113144856
|
T | C | 9 | a0001c0001t0001g0079a0001c0001t0001g0125a0001c0001t0001g0130others(6): Show | 9 | HG02109.hp1 HG02145.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.788+831T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144856 | ||||||
| chr10:113144898
|
C | T | 1 | a0001c0001t0011g0176 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.788+873C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144898 | ||||||
| chr10:113144921
|
T | A | 1 | a0001c0001t0009g0057 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.788+896T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144921 | ||||||
| chr10:113144967
|
T | C | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.788+942T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113144967 | ||||||
| chr10:113145114
|
G | GT | 68 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0031others(65): Show | 68 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.789-883dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113145114 | |||||
| chr10:113145114
|
GT | G | 38 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0044others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.789-883delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 113145114 | |||||
| chr10:113145197
|
C | T | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.789-814C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113145197 | ||||||
| chr10:113145496
|
C | T | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.789-515C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113145496 | ||||||
| chr10:113145842
|
G | A | 1 | a0001c0001t0029g0114 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.789-169G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 7/14 | chr10 | 113145842 | ||||||
| chr10:113146635
|
A | T | 34 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0038others(31): Show | 34 | HG00408.hp2 HG00438.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.875+538A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113146635 | ||||||
| chr10:113146784
|
G | A | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.875+687G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113146784 | ||||||
| chr10:113146851
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.875+754G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113146851 | ||||||
| chr10:113146901
|
T | TA | 32 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0038others(29): Show | 32 | HG00408.hp2 HG00438.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.875+813dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 113146901 | |||||
| chr10:113146910
|
AC | A | 3 | a0001c0001t0002g0006a0001c0001t0002g0094a0001c0005t0006g0138 | 3 | HG02886.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.875+814delC | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113146910 | ||||||
| chr10:113146955
|
G | A | 166 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.875+858G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113146955 | ||||||
| chr10:113146964
|
TA | T | 3 | a0001c0001t0001g0049a0001c0001t0002g0115a0008c0009t0002g0105 | 3 | HG00140.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.875+868delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113146964 | ||||||
| chr10:113146966
|
T | G | 3 | a0001c0001t0001g0049a0001c0001t0002g0115a0008c0009t0002g0105 | 3 | HG00140.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.875+869T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113146966 | ||||||
| chr10:113147083
|
C | T | 1 | a0001c0001t0046g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.875+986C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147083 | ||||||
| chr10:113147197
|
G | A | 4 | a0001c0001t0008g0139a0001c0004t0008g0144a0001c0004t0008g0146others(1): Show | 4 | HG01109.hp2 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.875+1100G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147197 | ||||||
| chr10:113147265
|
G | A | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.875+1168G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147265 | ||||||
| chr10:113147288
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.875+1191C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147288 | ||||||
| chr10:113147296
|
A | G | 73 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0036others(70): Show | 73 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.875+1199A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147296 | ||||||
| chr10:113147414
|
C | T | 1 | a0001c0001t0002g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.875+1317C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147414 | ||||||
| chr10:113147427
|
G | A | 1 | a0002c0002t0003g0162 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.875+1330G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147427 | ||||||
| chr10:113147499
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0002g0095others(4): Show | 7 | HG01109.hp1 HG01981.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.875+1402A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147499 | ||||||
| chr10:113147586
|
C | T | 2 | a0001c0001t0007g0032a0002c0002t0001g0088 | 2 | HG00597.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.875+1489C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147586 | ||||||
| chr10:113147689
|
T | C | 1 | a0001c0001t0033g0003 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875+1592T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147689 | ||||||
| chr10:113147927
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.875+1830C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147927 | ||||||
| chr10:113147935
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.875+1838C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113147935 | ||||||
| chr10:113148405
|
T | G | 1 | a0001c0001t0005g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.875+2308T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148405 | ||||||
| chr10:113148490
|
C | T | 1 | a0008c0009t0002g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.875+2393C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148490 | ||||||
| chr10:113148670
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0155a0001c0001t0002g0158 | 3 | HG01884.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.876-2328G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148670 | ||||||
| chr10:113148756
|
G | A | 1 | a0001c0001t0013g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.876-2242G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148756 | ||||||
| chr10:113148837
|
C | T | 2 | a0001c0001t0030g0004a0003c0003t0032g0011 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.876-2161C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148837 | ||||||
| chr10:113148840
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0009g0057a0001c0001t0043g0168 | 3 | HG00323.hp2 HG01358.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.876-2158G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148840 | ||||||
| chr10:113148932
|
G | A | 1 | a0001c0001t0013g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.876-2066G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148932 | ||||||
| chr10:113148957
|
C | T | 19 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0131others(16): Show | 19 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.876-2041C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148957 | ||||||
| chr10:113148969
|
C | T | 2 | a0001c0001t0009g0057a0001c0001t0043g0168 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.876-2029C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113148969 | ||||||
| chr10:113149223
|
G | C | 196 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.876-1775G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113149223 | ||||||
| chr10:113149669
|
CCTCATTA others(84): Show |
C | 1 | a0001c0001t0038g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.876-1326_876-1236d others(93): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 113149669 | |||||
| chr10:113149812
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.876-1186C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113149812 | ||||||
| chr10:113149972
|
C | T | 35 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(32): Show | 35 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.876-1026C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113149972 | ||||||
| chr10:113149980
|
T | A | 184 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.876-1018T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113149980 | ||||||
| chr10:113150128
|
A | C | 1 | a0001c0001t0010g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.876-870A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113150128 | ||||||
| chr10:113150161
|
A | T | 40 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(37): Show | 40 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.876-837A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113150161 | ||||||
| chr10:113150320
|
C | CT | 21 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(18): Show | 21 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.876-667dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 113150320 | |||||
| chr10:113150434
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.876-564C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113150434 | ||||||
| chr10:113150436
|
C | T | 2 | a0001c0001t0009g0057a0001c0001t0043g0168 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.876-562C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113150436 | ||||||
| chr10:113150653
|
G | C | 1 | a0001c0001t0003g0163 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.876-345G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113150653 | ||||||
| chr10:113150691
|
C | T | 14 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0002g0012others(11): Show | 14 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.876-307C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | chr10 | 113150691 | ||||||
| chr10:113150908
|
G | GT | 17 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(14): Show | 17 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.876-79dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 113150908 | |||||
| chr10:113151153
|
C | T | 1 | a0001c0001t0003g0163 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1001+30C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 9/14 | chr10 | 113151153 | ||||||
| chr10:113151263
|
T | C | 3 | a0001c0001t0004g0075a0001c0001t0030g0004a0003c0003t0032g0011 | 3 | HG02717.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1001+140T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 9/14 | chr10 | 113151263 | ||||||
| chr10:113151320
|
T | C | 183 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1001+197T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 9/14 | chr10 | 113151320 | ||||||
| chr10:113151385
|
T | C | 1 | a0001c0001t0003g0182 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1001+262T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 9/14 | chr10 | 113151385 | ||||||
| chr10:113152215
|
C | T | 4 | a0001c0001t0008g0148a0001c0004t0008g0144a0001c0004t0008g0146others(1): Show | 4 | HG01109.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-118C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 10/14 | chr10 | 113152215 | ||||||
| chr10:113152260
|
G | A | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1162-73G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 10/14 | chr10 | 113152260 | ||||||
| chr10:113152322
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0006g0157a0001c0001t0011g0175 | 3 | HG01081.hp1 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1162-11G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 10/14 | chr10 | 113152322 | ||||||
| chr10:113152448
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp2 | splice_region_variant&intron_variant | LOW | c.1269+8G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113152448 | ||||||
| chr10:113152498
|
C | T | 3 | a0001c0001t0006g0188a0001c0001t0010g0127a0001c0001t0014g0055 | 3 | HG01243.hp2 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1269+58C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113152498 | ||||||
| chr10:113152566
|
G | C | 1 | a0005c0010t0003g0167 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1269+126G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113152566 | ||||||
| chr10:113152775
|
C | T | 13 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(10): Show | 13 | HG01070.hp2 HG01099.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1269+335C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113152775 | ||||||
| chr10:113152897
|
G | A | 21 | a0001c0001t0001g0019a0001c0001t0002g0113a0001c0001t0002g0118others(18): Show | 21 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.1269+457G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113152897 | ||||||
| chr10:113153036
|
C | T | 2 | a0001c0001t0030g0004a0003c0003t0032g0011 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1269+596C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153036 | ||||||
| chr10:113153206
|
A | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0002g0096others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1269+766A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153206 | ||||||
| chr10:113153211
|
C | T | 13 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(10): Show | 13 | HG01070.hp2 HG01099.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1269+771C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153211 | ||||||
| chr10:113153224
|
G | A | 13 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(10): Show | 13 | HG01070.hp2 HG01099.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1269+784G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153224 | ||||||
| chr10:113153279
|
T | G | 11 | a0001c0001t0001g0068a0001c0001t0003g0163a0001c0001t0004g0134others(8): Show | 11 | HG00140.hp2 HG00323.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1269+839T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153279 | ||||||
| chr10:113153341
|
A | G | 2 | a0001c0001t0001g0019a0002c0002t0001g0088 | 2 | HG00408.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1269+901A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153341 | ||||||
| chr10:113153497
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1269+1057C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153497 | ||||||
| chr10:113153719
|
G | T | 4 | a0001c0001t0005g0122a0001c0001t0022g0050a0001c0001t0025g0035others(1): Show | 4 | HG01070.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1269+1279G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153719 | ||||||
| chr10:113153791
|
C | T | 9 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0004g0126others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1269+1351C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153791 | ||||||
| chr10:113153800
|
A | T | 13 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(10): Show | 13 | HG01070.hp2 HG01099.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1269+1360A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153800 | ||||||
| chr10:113153959
|
G | A | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1269+1519G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113153959 | ||||||
| chr10:113154100
|
C | G | 21 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0125others(18): Show | 21 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1269+1660C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154100 | ||||||
| chr10:113154245
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1269+1805C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154245 | ||||||
| chr10:113154462
|
C | A | 14 | a0001c0001t0001g0066a0001c0001t0001g0123a0001c0001t0002g0006others(11): Show | 14 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1269+2022C>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154462 | ||||||
| chr10:113154680
|
G | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0094a0001c0001t0011g0176others(2): Show | 5 | HG02886.hp1 NA18522.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1269+2240G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154680 | ||||||
| chr10:113154823
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1269+2383A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154823 | ||||||
| chr10:113154906
|
C | T | 159 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1269+2466C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154906 | ||||||
| chr10:113154944
|
G | C | 30 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0101others(27): Show | 30 | HG00738.hp2 HG01884.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1269+2504G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154944 | ||||||
| chr10:113154949
|
TA | T | 30 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0101others(27): Show | 30 | HG00738.hp2 HG01884.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1269+2510delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154949 | ||||||
| chr10:113154953
|
G | C | 179 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1269+2513G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113154953 | ||||||
| chr10:113154982
|
AT | A | 174 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1269+2560delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 113154982 | |||||
| chr10:113154982
|
ATT | A | 5 | a0001c0001t0001g0047a0001c0001t0002g0094a0001c0001t0003g0179others(2): Show | 5 | HG01256.hp1 HG01256.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1269+2559_1269+256 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 113154982 | |||||
| chr10:113155058
|
C | G | 4 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0002g0142others(1): Show | 4 | HG02109.hp1 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1269+2618C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155058 | ||||||
| chr10:113155154
|
T | G | 14 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(11): Show | 14 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1269+2714T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155154 | ||||||
| chr10:113155308
|
A | T | 1 | a0001c0001t0017g0052 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1270-2713A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155308 | ||||||
| chr10:113155321
|
C | G | 14 | a0001c0001t0001g0066a0001c0001t0001g0123a0001c0001t0002g0006others(11): Show | 14 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.1270-2700C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155321 | ||||||
| chr10:113155455
|
G | T | 111 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1270-2566G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155455 | ||||||
| chr10:113155470
|
C | T | 2 | a0001c0001t0001g0197a0002c0002t0001g0028 | 2 | HG02683.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1270-2551C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155470 | ||||||
| chr10:113155641
|
G | A | 1 | a0001c0004t0008g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1270-2380G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155641 | ||||||
| chr10:113155768
|
G | T | 1 | a0001c0001t0013g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1270-2253G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113155768 | ||||||
| chr10:113156115
|
CT | C | 145 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1270-1888delT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 113156115 | |||||
| chr10:113156115
|
CTT | C | 5 | a0001c0001t0001g0019a0001c0001t0002g0104a0001c0001t0005g0064others(2): Show | 5 | HG00323.hp1 HG00408.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1270-1889_1270-188 others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 113156115 | |||||
| chr10:113156120
|
T | C | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1270-1901T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156120 | ||||||
| chr10:113156133
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1270-1888T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156133 | ||||||
| chr10:113156240
|
C | G | 182 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1270-1781C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156240 | ||||||
| chr10:113156261
|
T | C | 3 | a0001c0001t0006g0188a0001c0001t0010g0127a0001c0001t0014g0055 | 3 | HG01243.hp2 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1270-1760T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156261 | ||||||
| chr10:113156361
|
G | A | 2 | a0001c0001t0010g0098a0001c0001t0013g0151 | 2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1270-1660G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156361 | ||||||
| chr10:113156506
|
G | A | 2 | a0001c0001t0028g0014a0001c0001t0037g0160 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1270-1515G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156506 | ||||||
| chr10:113156685
|
G | A | 2 | a0001c0001t0028g0014a0001c0001t0037g0160 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1270-1336G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156685 | ||||||
| chr10:113156827
|
G | T | 97 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0029others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.1270-1194G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156827 | ||||||
| chr10:113156940
|
T | C | 1 | a0001c0001t0026g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1270-1081T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113156940 | ||||||
| chr10:113157067
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1270-954G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157067 | ||||||
| chr10:113157104
|
T | G | 18 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0001g0125others(15): Show | 18 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270-917T>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157104 | ||||||
| chr10:113157187
|
C | T | 1 | a0006c0012t0007g0026 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1270-834C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157187 | ||||||
| chr10:113157204
|
C | T | 2 | a0001c0001t0028g0014a0001c0001t0037g0160 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1270-817C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157204 | ||||||
| chr10:113157280
|
G | A | 3 | a0001c0001t0004g0075a0001c0001t0030g0004a0003c0003t0032g0011 | 3 | HG02717.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1270-741G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157280 | ||||||
| chr10:113157454
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1270-567C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157454 | ||||||
| chr10:113157569
|
A | T | 3 | a0001c0001t0001g0101a0001c0001t0002g0102a0001c0001t0004g0132 | 3 | HG00738.hp2 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1270-452A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157569 | ||||||
| chr10:113157580
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0009g0057a0001c0001t0043g0168 | 3 | HG00323.hp2 HG01358.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1270-441G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157580 | ||||||
| chr10:113157609
|
C | T | 1 | a0002c0002t0001g0090 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1270-412C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157609 | ||||||
| chr10:113157683
|
T | C | 14 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(11): Show | 14 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1270-338T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157683 | ||||||
| chr10:113157797
|
A | G | 1 | a0002c0002t0003g0171 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1270-224A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 11/14 | chr10 | 113157797 | ||||||
| chr10:113158360
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1318+291C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 12/14 | chr10 | 113158360 | ||||||
| chr10:113159146
|
C | CT | 9 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0004g0126others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1369+437dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 113159146 | |||||
| chr10:113159161
|
G | GT | 19 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(16): Show | 19 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1369+450dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 113159161 | |||||
| chr10:113159332
|
A | T | 1 | a0001c0001t0039g0166 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1370-588A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159332 | ||||||
| chr10:113159413
|
G | A | 6 | a0001c0001t0008g0148a0001c0001t0028g0014a0001c0001t0037g0160others(3): Show | 6 | HG01109.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-507G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159413 | ||||||
| chr10:113159723
|
A | G | 15 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(12): Show | 15 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1370-197A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159723 | ||||||
| chr10:113159830
|
TCC | T | 12 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0002g0128others(9): Show | 12 | HG00140.hp2 HG01123.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1370-76_1370-75del others(2): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 113159830 | |||||
| chr10:113159840
|
C | T | 2 | a0001c0001t0030g0004a0003c0003t0032g0011 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1370-80C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159840 | ||||||
| chr10:113159841
|
C | T | 23 | a0001c0001t0001g0058a0001c0001t0001g0123a0001c0001t0002g0012others(20): Show | 23 | HG00323.hp2 HG01109.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.1370-79C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159841 | ||||||
| chr10:113159842
|
C | CCT | 14 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0047others(11): Show | 14 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1370-77_1370-76ins others(2): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 113159842 | |||||
| chr10:113159842
|
C | CCTCCCTC others(1): Show |
13 | a0001c0001t0001g0061a0001c0001t0001g0082a0001c0001t0001g0190others(10): Show | 13 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1370-77_1370-76ins others(8): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 113159842 | |||||
| chr10:113159842
|
C | CT | 2 | a0001c0001t0002g0117a0001c0001t0010g0098 | 2 | HG01515.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1370-78_1370-77ins others(1): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159842 | ||||||
| chr10:113159842
|
C | CTCCCTCT | 25 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0049others(22): Show | 25 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1370-78_1370-77ins others(7): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159842 | ||||||
| chr10:113159842
|
C | CTCT | 3 | a0001c0001t0002g0094a0001c0001t0011g0176a0001c0005t0006g0138 | 3 | NA18522.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1370-78_1370-77ins others(3): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159842 | ||||||
| chr10:113159842
|
C | T | 43 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0034others(40): Show | 43 | HG00323.hp1 HG00642.hp1 HG01256.hp2 others(40): Show |
intron_variant | MODIFIER | c.1370-78C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159842 | ||||||
| chr10:113159844
|
C | CCTCT | 12 | a0001c0001t0001g0017a0001c0001t0001g0129a0001c0001t0002g0095others(9): Show | 12 | HG00738.hp1 HG01099.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1370-75_1370-72dup others(4): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 113159844 | |||||
| chr10:113159844
|
C | CCTCTCT | 47 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0034others(44): Show | 47 | HG00323.hp1 HG00642.hp1 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1370-72_1370-71ins others(6): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 113159844 | |||||
| chr10:113159844
|
C | CTCCCTCT others(2): Show |
3 | a0001c0001t0001g0056a0001c0005t0019g0001a0002c0002t0001g0088 | 3 | HG00597.hp2 HG02897.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1370-76_1370-75ins others(9): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159844 | ||||||
| chr10:113159844
|
C | CTCT | 5 | a0001c0001t0001g0086a0001c0001t0002g0143a0001c0001t0005g0064others(2): Show | 5 | HG00140.hp1 HG00741.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-76_1370-75ins others(3): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159844 | ||||||
| chr10:113159844
|
C | CTCTCT | 28 | a0001c0001t0001g0018a0001c0001t0001g0046a0001c0001t0001g0058others(25): Show | 28 | HG00323.hp2 HG00735.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1370-76_1370-75ins others(5): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159844 | ||||||
| chr10:113159844
|
C | T | 62 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0041others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1370-76C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159844 | ||||||
| chr10:113159889
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1370-31C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 13/14 | chr10 | 113159889 | ||||||
| chr10:113160015
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1442+23G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160015 | ||||||
| chr10:113160212
|
C | T | 2 | a0001c0001t0030g0004a0003c0003t0032g0011 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1442+220C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160212 | ||||||
| chr10:113160236
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1442+244C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160236 | ||||||
| chr10:113160330
|
A | G | 23 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0193others(20): Show | 23 | HG00140.hp2 HG01070.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1442+338A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160330 | ||||||
| chr10:113160348
|
C | T | 2 | a0001c0001t0034g0187a0001c0001t0041g0180 | 2 | HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1442+356C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160348 | ||||||
| chr10:113160444
|
A | T | 5 | a0001c0001t0004g0075a0001c0001t0010g0098a0001c0001t0030g0004others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442+452A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160444 | ||||||
| chr10:113160445
|
T | A | 1 | a0001c0001t0004g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1442+453T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160445 | ||||||
| chr10:113160720
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1442+728A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160720 | ||||||
| chr10:113160753
|
C | G | 2 | a0001c0001t0026g0124a0003c0003t0011g0009 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1442+761C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113160753 | ||||||
| chr10:113161117
|
T | C | 1 | a0001c0001t0008g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1442+1125T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113161117 | ||||||
| chr10:113161663
|
T | C | 1 | a0001c0001t0004g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1442+1671T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113161663 | ||||||
| chr10:113161731
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1442+1739G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113161731 | ||||||
| chr10:113161762
|
C | T | 6 | a0001c0001t0008g0148a0001c0001t0028g0014a0001c0001t0037g0160others(3): Show | 6 | HG01109.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1442+1770C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113161762 | ||||||
| chr10:113161879
|
T | A | 3 | a0001c0001t0004g0075a0001c0001t0030g0004a0003c0003t0032g0011 | 3 | HG02717.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1442+1887T>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113161879 | ||||||
| chr10:113161902
|
G | T | 10 | a0001c0001t0001g0068a0001c0001t0004g0134a0001c0001t0008g0148others(7): Show | 10 | HG00323.hp2 HG01109.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1442+1910G>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113161902 | ||||||
| chr10:113161954
|
A | T | 9 | a0001c0001t0001g0101a0001c0001t0002g0102a0001c0001t0004g0132others(6): Show | 9 | HG00738.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1442+1962A>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113161954 | ||||||
| chr10:113162002
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0099a0001c0001t0004g0126others(6): Show | 9 | HG02257.hp1 HG02572.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1442+2010G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113162002 | ||||||
| chr10:113162162
|
G | C | 2 | a0001c0001t0001g0101a0001c0001t0002g0102 | 2 | HG00738.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1442+2170G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113162162 | ||||||
| chr10:113162284
|
G | A | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1442+2292G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113162284 | ||||||
| chr10:113162315
|
ATGGGGTG others(2): Show |
A | 3 | a0001c0001t0006g0188a0001c0001t0010g0127a0001c0001t0014g0055 | 3 | HG01243.hp2 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1442+2327_1442+233 others(13): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr10 | 113162315 | |||||
| chr10:113162536
|
T | C | 1 | a0002c0002t0007g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1442+2544T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113162536 | ||||||
| chr10:113162644
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1442+2652G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113162644 | ||||||
| chr10:113162679
|
T | C | 1 | a0001c0001t0007g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1442+2687T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113162679 | ||||||
| chr10:113162931
|
C | T | 2 | a0001c0001t0009g0081a0001c0001t0023g0027 | 2 | HG01106.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1443-2624C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113162931 | ||||||
| chr10:113163009
|
T | TA | 7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0002g0117others(4): Show | 7 | HG01071.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1443-2531dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr10 | 113163009 | |||||
| chr10:113163009
|
TA | T | 5 | a0001c0001t0001g0029a0001c0001t0006g0136a0001c0001t0013g0119others(2): Show | 5 | HG02132.hp1 HG02717.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1443-2531delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr10 | 113163009 | |||||
| chr10:113163352
|
T | C | 3 | a0001c0001t0001g0191a0001c0001t0002g0161a0002c0002t0001g0200 | 3 | HG00597.hp1 HG02523.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1443-2203T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113163352 | ||||||
| chr10:113163653
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1443-1902A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113163653 | ||||||
| chr10:113163654
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1443-1901C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113163654 | ||||||
| chr10:113163660
|
C | G | 14 | a0001c0001t0001g0123a0001c0001t0002g0006a0001c0001t0002g0094others(11): Show | 14 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1443-1895C>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113163660 | ||||||
| chr10:113163877
|
C | T | 2 | a0001c0001t0030g0004a0003c0003t0032g0011 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1443-1678C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113163877 | ||||||
| chr10:113163955
|
G | A | 2 | a0001c0001t0002g0117a0001c0001t0017g0052 | 2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1443-1600G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113163955 | ||||||
| chr10:113163999
|
G | C | 1 | a0001c0001t0002g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1443-1556G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113163999 | ||||||
| chr10:113164066
|
C | T | 59 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0031others(56): Show | 59 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1443-1489C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164066 | ||||||
| chr10:113164420
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1443-1135C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164420 | ||||||
| chr10:113164460
|
C | T | 1 | a0001c0001t0018g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1443-1095C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164460 | ||||||
| chr10:113164461
|
G | A | 8 | a0001c0001t0001g0074a0001c0001t0004g0126a0001c0001t0004g0133others(5): Show | 8 | HG01109.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1443-1094G>A | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164461 | ||||||
| chr10:113164583
|
A | C | 1 | a0001c0001t0002g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1443-972A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164583 | ||||||
| chr10:113164596
|
T | TA | 21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0029others(18): Show | 21 | HG00140.hp2 HG00738.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1443-943dupA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr10 | 113164596 | |||||
| chr10:113164596
|
TA | T | 65 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0041others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1443-943delA | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr10 | 113164596 | |||||
| chr10:113164607
|
A | C | 2 | a0001c0001t0004g0132a0001c0001t0011g0176 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1443-948A>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164607 | ||||||
| chr10:113164669
|
C | T | 89 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0038others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1443-886C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164669 | ||||||
| chr10:113164754
|
C | CT | 8 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0002g0115others(5): Show | 8 | HG00140.hp2 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1443-793dupT | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr10 | 113164754 | |||||
| chr10:113164760
|
T | C | 1 | a0001c0001t0005g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1443-795T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164760 | ||||||
| chr10:113164786
|
T | C | 1 | a0002c0002t0001g0028 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1443-769T>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113164786 | ||||||
| chr10:113165008
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0115 | 2 | HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1443-547C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113165008 | ||||||
| chr10:113165051
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0037g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1443-490_1443-477d others(16): Show |
TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr10 | 113165051 | |||||
| chr10:113165132
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1443-423C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113165132 | ||||||
| chr10:113165201
|
A | G | 1 | a0001c0001t0010g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1443-354A>G | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113165201 | ||||||
| chr10:113165263
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1443-292C>T | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113165263 | ||||||
| chr10:113165401
|
G | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0086 | 2 | HG01981.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1443-154G>C | TCF7L2 | ENSG00000148737.18 | transcript | ENST00000355995.9 | protein_coding | 14/14 | chr10 | 113165401 |