Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83439 |
| ensemblid | ENSG00000152284.5 |
| hgncid | 11640 |
| symbol | TCF7L1 |
| name | transcription factor 7 like 1 |
| refseq_nuc | NM_031283.3 |
| refseq_prot | NP_112573.1 |
| ensembl_nuc | ENST00000282111.4 |
| ensembl_prot | ENSP00000282111.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 85133392 |
| end | 85310387 |
| strand | + |
| ver | v1.2 |
| region | chr2:85133392-85310387 |
| region5000 | chr2:85128392-85315387 |
| regionname0 | TCF7L1_chr2_85133392_85310387 |
| regionname5000 | TCF7L1_chr2_85128392_85315387 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 588 | 131 | 39 | 30 | 44 | 5 | 12 | 30 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0002 | 0/1 | 587 | 92 | 44 | 15 | 18 | 7 | 7 | 12 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(582): Show |
chr2 | 85128392 | 85315387 |
| a0003 | 0/0 | 588 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0004 | 0/0 | 588 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0005 | 0/0 | 588 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0006 | 0/0 | 588 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0007 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0008 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0009 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| a0010 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | MPQLG others(583): Show |
chr2 | 85128392 | 85315387 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1764 | 130 | 38 | 30 | 44 | 5 | 12 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0001c0016 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0002c0002 | 0/1 | 1761 | 84 | 36 | 15 | 18 | 7 | 7 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1756): Show |
chr2 | 85128392 | 85315387 | ||
| a0002c0003 | 0/0 | 1761 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1756): Show |
chr2 | 85128392 | 85315387 | ||
| a0002c0007 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1756): Show |
chr2 | 85128392 | 85315387 | ||
| a0002c0008 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1756): Show |
chr2 | 85128392 | 85315387 | ||
| a0002c0009 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1756): Show |
chr2 | 85128392 | 85315387 | ||
| a0002c0010 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1756): Show |
chr2 | 85128392 | 85315387 | ||
| a0003c0004 | 0/0 | 1764 | 3 | 0 | 2 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0004c0005 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0004c0012 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0005c0006 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0006c0017 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0007c0013 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0008c0015 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0009c0014 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 | ||
| a0010c0011 | 0/0 | 1764 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | ATGCC others(1759): Show |
chr2 | 85128392 | 85315387 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2985 | 86 | 24 | 18 | 32 | 2 | 10 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0001c0001t0002 | 1/0 | 2985 | 37 | 14 | 8 | 11 | 1 | 2 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0001c0001t0005 | 0/0 | 2985 | 3 | 0 | 2 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0001c0001t0006 | 0/0 | 2985 | 2 | 0 | 1 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0001c0001t0007 | 0/0 | 2985 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0001c0001t0011 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0001c0016t0001 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0002c0002t0001 | 0/0 | 2982 | 43 | 20 | 7 | 7 | 4 | 5 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0002t0002 | 0/1 | 2982 | 20 | 11 | 3 | 3 | 1 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0002t0003 | 0/0 | 2982 | 15 | 1 | 4 | 7 | 2 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0002t0004 | 0/0 | 2982 | 3 | 1 | 1 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0002t0007 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0002t0008 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0002t0012 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0003t0002 | 0/0 | 2982 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0007t0002 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0008t0002 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0009t0001 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0002c0010t0001 | 0/0 | 2982 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2977): Show |
chr2 | 85128392 | 85315387 |
| a0003c0004t0002 | 0/0 | 2985 | 3 | 0 | 2 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0004c0005t0001 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0004c0005t0009 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0004c0012t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0005c0006t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0005c0006t0010 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0006c0017t0001 | 0/0 | 2985 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0007c0013t0001 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0008c0015t0001 | 0/0 | 2985 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0009c0014t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| a0010c0011t0002 | 0/0 | 2985 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | GCTCG others(2980): Show |
chr2 | 85128392 | 85315387 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0001c0016t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0002t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0007t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0008t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0009t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0002c0010t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0003c0004t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0003c0004t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0003c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0004c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0004c0005t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0004c0012t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0005c0006t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0005c0006t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0006c0017t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0007c0013t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0008c0015t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0009c0014t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| a0010c0011t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0194 | EUR | FIN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00735 | hp2 | a0003 | c0004 | t0002 | g0106 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00741 | hp1 | a0002 | c0002 | t0004 | g0072 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01168 | hp2 | a0006 | c0017 | t0001 | g0215 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0134 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0068 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0064 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0074 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0050 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0051 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01517 | hp2 | a0002 | c0002 | t0003 | g0073 | EUR | IBS | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01952 | hp1 | a0002 | c0002 | t0003 | g0071 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0176 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01981 | hp1 | a0002 | c0002 | t0003 | g0070 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02056 | hp2 | a0002 | c0002 | t0004 | g0055 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0080 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02135 | hp1 | a0007 | c0013 | t0001 | g0143 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02148 | hp2 | a0003 | c0004 | t0002 | g0114 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02165 | hp1 | a0008 | c0015 | t0001 | g0227 | EAS | CDX | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02257 | hp1 | a0009 | c0014 | t0002 | g0164 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02451 | hp1 | a0002 | c0003 | t0002 | g0036 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02451 | hp2 | a0002 | c0002 | t0012 | g0021 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02523 | hp2 | a0001 | c0001 | t0011 | g0142 | EAS | KHV | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02572 | hp1 | a0002 | c0003 | t0002 | g0086 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02615 | hp1 | a0002 | c0008 | t0002 | g0041 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02615 | hp2 | a0004 | c0005 | t0001 | g0135 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02647 | hp1 | a0005 | c0006 | t0002 | g0137 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02647 | hp2 | a0002 | c0007 | t0002 | g0029 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02723 | hp1 | a0005 | c0006 | t0010 | g0233 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02895 | hp2 | a0002 | c0009 | t0001 | g0019 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02965 | hp2 | a0002 | c0002 | t0007 | g0006 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03041 | hp2 | a0004 | c0005 | t0009 | g0204 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03139 | hp1 | a0002 | c0003 | t0002 | g0082 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03195 | hp1 | a0002 | c0010 | t0001 | g0186 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04115 | hp1 | a0003 | c0004 | t0002 | g0115 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0083 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0026 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18522 | hp2 | a0002 | c0002 | t0004 | g0085 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18966 | hp1 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18975 | hp2 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18998 | hp1 | a0002 | c0002 | t0003 | g0146 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19030 | hp2 | a0004 | c0012 | t0002 | g0184 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19043 | hp1 | a0002 | c0003 | t0002 | g0188 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0235 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | ASW | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | ASW | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0002 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0065 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0023 | EUR | TSI | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | GIH | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | GIH | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02559 | hp1 | a0002 | c0002 | t0008 | g0059 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG03471 | hp2 | a0010 | c0011 | t0002 | g0231 | AFR | MSL | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| NA21309 | hp2 | a0001 | c0016 | t0001 | g0203 | AFR | LWK | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0028 | REF | REF | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0216 | REF | REF | TCF7L1_chr2_85128392_85315387 | TCF7L1 | chr2 | 85128392 | 85315387 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85133705 | GGGC | G | 1 | a0002 | 91 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(88): Show |
conservative_inframe_deletion | MODERATE | c.40_42delGGC | p.Gly14del | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | 333/2985 | 40/1767 | 14/588 | INFO_REALIGN_3_PRIME | chr2 | 85133705 | ||
| chr2:85134038 | T | C | 1 | a0010 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.272T>C | p.Val91Ala | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 2/12 | 565/2985 | 272/1767 | 91/588 | chr2 | 85134038 | |||
| chr2:85283531 | T | A | 2 | a0002 a0004 |
7 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
missense_variant | MODERATE | c.478T>A | p.Ser160Thr | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/12 | 771/2985 | 478/1767 | 160/588 | chr2 | 85283531 | |||
| chr2:85303946 | C | G | 1 | a0002 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.710C>G | p.Ser237Cys | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 6/12 | 1003/2985 | 710/1767 | 237/588 | chr2 | 85303946 | |||
| chr2:85305288 | A | G | 1 | a0006 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.874A>G | p.Met292Val | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/12 | 1167/2985 | 874/1767 | 292/588 | chr2 | 85305288 | |||
| chr2:85305331 | C | T | 1 | a0002 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.917C>T | p.Pro306Leu | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/12 | 1210/2985 | 917/1767 | 306/588 | chr2 | 85305331 | |||
| chr2:85309235 | C | A | 1 | a0007 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1540C>A | p.Gln514Lys | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1833/2985 | 1540/1767 | 514/588 | chr2 | 85309235 | |||
| chr2:85309241 | G | T | 1 | a0008 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1546G>T | p.Ala516Ser | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1839/2985 | 1546/1767 | 516/588 | chr2 | 85309241 | |||
| chr2:85309292 | G | A | 1 | a0003 | 3 | HG00735.hp2 HG02148.hp2 HG04115.hp1 |
missense_variant | MODERATE | c.1597G>A | p.Gly533Arg | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1890/2985 | 1597/1767 | 533/588 | chr2 | 85309292 | |||
| chr2:85309385 | G | A | 1 | a0005 | 2 | HG02647.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.1690G>A | p.Ala564Thr | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1983/2985 | 1690/1767 | 564/588 | chr2 | 85309385 | |||
| chr2:85309442 | G | A | 1 | a0009 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1747G>A | p.Val583Ile | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 2040/2985 | 1747/1767 | 583/588 | chr2 | 85309442 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85306251 | C | T | 2 | a0001c0016 a0004c0005 |
3 | HG02615.hp2 HG03041.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1035C>T | p.His345His | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 9/12 | 1328/2985 | 1035/1767 | 345/588 | chr2 | 85306251 | |||
| chr2:85309111 | C | T | 1 | a0002c0008 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.1416C>T | p.His472His | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1709/2985 | 1416/1767 | 472/588 | chr2 | 85309111 | |||
| chr2:85309318 | C | T | 1 | a0002c0007 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.1623C>T | p.Leu541Leu | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 1916/2985 | 1623/1767 | 541/588 | chr2 | 85309318 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85133494 | C | T | 1 | a0002c0002t0012 | 1 | HG02451.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-191C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | chr2 | 85133494 | |||||||
| chr2:85133531 | G | A | 3 | a0002c0002t0003 a0002c0002t0004 a0002c0002t0008 |
19 | HG00741.hp1 HG01257.hp1 HG01515.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-154G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | 154 | chr2 | 85133531 | ||||||
| chr2:85133640 | C | A | 2 | a0001c0001t0005 a0001c0001t0006 |
5 | HG00639.hp1 HG01168.hp1 HG01261.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-45C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/12 | 45 | chr2 | 85133640 | ||||||
| chr2:85309603 | C | T | 2 | a0001c0001t0007 a0002c0002t0007 |
2 | HG01256.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 141 | chr2 | 85309603 | ||||||
| chr2:85309827 | C | T | 1 | a0001c0001t0011 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 365 | chr2 | 85309827 | ||||||
| chr2:85309887 | G | A | 3 | a0001c0001t0007 a0002c0002t0007 a0002c0002t0008 |
3 | HG01256.hp1 HG02559.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*425G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 425 | chr2 | 85309887 | ||||||
| chr2:85310075 | G | A | 1 | a0004c0005t0009 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 613 | chr2 | 85310075 | ||||||
| chr2:85310189 | G | A | 15 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0011 others(12): Show |
157 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*727G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 727 | chr2 | 85310189 | ||||||
| chr2:85310222 | G | A | 1 | a0005c0006t0010 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 12/12 | 760 | chr2 | 85310222 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:85133974 | T | TGCGTCCG others(1): Show |
8 | a0002c0002t0001g0007 a0002c0002t0001g0009 a0002c0002t0001g0010 others(5): Show |
8 | HG02145.hp1 HG02965.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-41_250-34dupGC others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 85133974 | ||||||
| chr2:85133978 | T | G | 5 | a0001c0001t0005g0001 a0001c0001t0005g0002 a0001c0001t0005g0004 others(2): Show |
5 | HG00639.hp1 HG01168.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-38T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 1/11 | chr2 | 85133978 | |||||||
| chr2:85134138 | C | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+59C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 2/11 | chr2 | 85134138 | |||||||
| chr2:85134227 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | NA18950.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.314-96G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 2/11 | chr2 | 85134227 | |||||||
| chr2:85134728 | C | T | 1 | a0002c0002t0003g0235 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.441+278C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85134728 | |||||||
| chr2:85134729 | G | A | 7 | a0001c0001t0005g0001 a0001c0001t0005g0002 a0001c0001t0006g0003 others(4): Show |
7 | HG01261.hp2 HG01516.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+279G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85134729 | |||||||
| chr2:85135216 | T | C | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.441+766T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135216 | |||||||
| chr2:85135622 | G | A | 1 | a0002c0002t0012g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.441+1172G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135622 | |||||||
| chr2:85135702 | G | C | 2 | a0002c0002t0001g0022 a0002c0002t0001g0023 |
2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.441+1252G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135702 | |||||||
| chr2:85135788 | G | A | 1 | a0002c0002t0002g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.441+1338G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135788 | |||||||
| chr2:85135789 | G | A | 1 | a0002c0002t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.441+1339G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135789 | |||||||
| chr2:85135790 | A | AGGTC | 49 | a0001c0001t0001g0031 a0001c0001t0002g0067 a0001c0001t0005g0004 others(46): Show |
49 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.441+1341_441+1344d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85135790 | ||||||
| chr2:85135810 | T | G | 9 | a0001c0001t0001g0031 a0001c0001t0005g0004 a0001c0001t0006g0005 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+1360T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135810 | |||||||
| chr2:85135931 | AG | A | 101 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0091 others(98): Show |
101 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.441+1492delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85135931 | ||||||
| chr2:85135931 | AGG | A | 81 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(78): Show |
81 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.441+1491_441+1492d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85135931 | ||||||
| chr2:85135933 | G | A | 7 | a0001c0001t0005g0001 a0001c0001t0005g0002 a0001c0001t0006g0003 others(4): Show |
7 | HG01261.hp2 HG01516.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+1483G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135933 | |||||||
| chr2:85135935 | G | C | 19 | a0001c0001t0001g0076 a0002c0002t0001g0069 a0002c0002t0001g0081 others(16): Show |
19 | HG00741.hp1 HG01257.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+1485G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85135935 | |||||||
| chr2:85136034 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+1584C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136034 | |||||||
| chr2:85136466 | CCAACCTT others(4): Show |
C | 1 | a0002c0002t0012g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.441+2018_441+2028d others(13): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85136466 | ||||||
| chr2:85136520 | G | A | 3 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 |
3 | HG02818.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.441+2070G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136520 | |||||||
| chr2:85136583 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.441+2133G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136583 | |||||||
| chr2:85136615 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.441+2165T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136615 | |||||||
| chr2:85136709 | G | C | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+2259G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136709 | |||||||
| chr2:85136832 | T | C | 1 | a0002c0002t0003g0068 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.441+2382T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136832 | |||||||
| chr2:85136970 | C | T | 42 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(39): Show |
42 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.441+2520C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85136970 | |||||||
| chr2:85137015 | C | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+2565C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137015 | |||||||
| chr2:85137184 | T | G | 37 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0032 others(34): Show |
37 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.441+2734T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137184 | |||||||
| chr2:85137414 | G | A | 29 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0183 others(26): Show |
29 | HG00741.hp1 HG01257.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.441+2964G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137414 | |||||||
| chr2:85137566 | T | C | 79 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0170 others(76): Show |
79 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.441+3116T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137566 | |||||||
| chr2:85137630 | G | C | 36 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0032 others(33): Show |
36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+3180G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137630 | |||||||
| chr2:85137646 | A | G | 11 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(8): Show |
11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+3196A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137646 | |||||||
| chr2:85137682 | C | T | 36 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0032 others(33): Show |
36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+3232C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137682 | |||||||
| chr2:85137701 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00597.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.441+3251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137701 | |||||||
| chr2:85137892 | CA | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0232 a0001c0001t0001g0234 others(5): Show |
8 | HG01167.hp1 HG01168.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+3459delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85137892 | ||||||
| chr2:85137906 | A | G | 2 | a0002c0002t0002g0020 a0002c0002t0002g0065 |
2 | HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.441+3456A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85137906 | |||||||
| chr2:85138244 | C | T | 36 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0032 others(33): Show |
36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+3794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138244 | |||||||
| chr2:85138375 | A | G | 107 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0090 others(104): Show |
107 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.441+3925A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138375 | |||||||
| chr2:85138394 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+3944T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138394 | |||||||
| chr2:85138446 | G | A | 10 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(7): Show |
10 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+3996G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138446 | |||||||
| chr2:85138492 | TTC | T | 2 | a0002c0002t0001g0087 a0004c0012t0002g0184 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+4044_441+4045d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85138492 | ||||||
| chr2:85138588 | C | T | 36 | a0002c0002t0001g0022 a0002c0002t0001g0023 a0002c0002t0001g0032 others(33): Show |
36 | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+4138C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138588 | |||||||
| chr2:85138843 | C | T | 2 | a0001c0001t0002g0067 a0002c0003t0002g0086 |
2 | HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.441+4393C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138843 | |||||||
| chr2:85138863 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.441+4413G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85138863 | |||||||
| chr2:85139195 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.441+4745G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139195 | |||||||
| chr2:85139703 | C | G | 1 | a0002c0002t0001g0064 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.441+5253C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139703 | |||||||
| chr2:85139831 | G | C | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441+5381G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139831 | |||||||
| chr2:85139848 | T | G | 78 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0170 others(75): Show |
78 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.441+5398T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139848 | |||||||
| chr2:85139864 | T | G | 22 | a0001c0001t0001g0092 a0001c0001t0001g0170 a0001c0001t0001g0171 others(19): Show |
22 | HG01175.hp2 HG01256.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.441+5414T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139864 | |||||||
| chr2:85139958 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0170 a0001c0001t0001g0171 others(18): Show |
21 | HG01175.hp2 HG01256.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+5508G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85139958 | |||||||
| chr2:85140088 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+5638G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140088 | |||||||
| chr2:85140155 | C | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+5705C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140155 | |||||||
| chr2:85140201 | A | G | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+5751A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140201 | |||||||
| chr2:85140480 | T | TC | 165 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0088 others(162): Show |
165 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.441+6032dupC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85140480 | ||||||
| chr2:85140501 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+6051G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140501 | |||||||
| chr2:85140605 | C | T | 5 | a0002c0002t0001g0089 a0002c0002t0002g0016 a0002c0002t0002g0018 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+6155C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140605 | |||||||
| chr2:85140619 | TG | T | 207 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(204): Show |
207 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(204): Show |
intron_variant | MODIFIER | c.441+6171delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85140619 | ||||||
| chr2:85140685 | G | A | 29 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0170 others(26): Show |
29 | HG01071.hp2 HG01175.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.441+6235G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140685 | |||||||
| chr2:85140732 | G | A | 111 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0091 others(108): Show |
111 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.441+6282G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140732 | |||||||
| chr2:85140767 | A | G | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+6317A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140767 | |||||||
| chr2:85140896 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.441+6446C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140896 | |||||||
| chr2:85140899 | A | G | 1 | a0002c0002t0003g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.441+6449A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140899 | |||||||
| chr2:85140904 | A | G | 3 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0005c0006t0010g0233 |
3 | HG02723.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.441+6454A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140904 | |||||||
| chr2:85140913 | C | CAGAG | 161 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(158): Show |
161 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.441+6466_441+6467i others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85140913 | ||||||
| chr2:85140939 | C | T | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+6489C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140939 | |||||||
| chr2:85140967 | G | C | 31 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0170 others(28): Show |
31 | HG01071.hp2 HG01175.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+6517G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85140967 | |||||||
| chr2:85141127 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.441+6677A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141127 | |||||||
| chr2:85141205 | A | T | 15 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(12): Show |
15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+6755A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141205 | |||||||
| chr2:85141220 | C | CAG | 190 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(187): Show |
190 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(187): Show |
intron_variant | MODIFIER | c.441+6771_441+6772d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85141220 | ||||||
| chr2:85141282 | A | G | 2 | a0001c0001t0001g0088 a0002c0003t0002g0086 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.441+6832A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141282 | |||||||
| chr2:85141443 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.441+6993G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141443 | |||||||
| chr2:85141510 | A | G | 4 | a0002c0002t0001g0057 a0002c0002t0002g0017 a0002c0002t0002g0058 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+7060A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141510 | |||||||
| chr2:85141625 | A | T | 15 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(12): Show |
15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+7175A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141625 | |||||||
| chr2:85141856 | T | A | 6 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(3): Show |
6 | HG02257.hp1 HG02647.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+7406T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85141856 | |||||||
| chr2:85142034 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+7584T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142034 | |||||||
| chr2:85142137 | C | T | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(6): Show |
9 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+7687C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142137 | |||||||
| chr2:85142169 | G | A | 1 | a0002c0002t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+7719G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142169 | |||||||
| chr2:85142195 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+7745G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142195 | |||||||
| chr2:85142258 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(157): Show |
160 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.441+7808T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142258 | |||||||
| chr2:85142340 | G | A | 1 | a0002c0002t0003g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.441+7890G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142340 | |||||||
| chr2:85142431 | AATGTGTG others(8): Show |
A | 2 | a0002c0002t0001g0087 a0004c0012t0002g0184 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+7982_441+7996d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142431 | |||||||
| chr2:85142432 | ATGTG | A | 24 | a0001c0001t0001g0160 a0001c0001t0001g0212 a0001c0001t0001g0213 others(21): Show |
24 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+8012_441+8015d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | ||||||
| chr2:85142432 | ATGTGTG | A | 14 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0002g0147 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+8010_441+8015d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | ||||||
| chr2:85142432 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.441+8002_441+8015d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | ||||||
| chr2:85142432 | ATGTGTGT others(8): Show |
A | 14 | a0001c0001t0001g0090 a0001c0001t0002g0167 a0002c0002t0001g0007 others(11): Show |
14 | HG00735.hp1 HG02145.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+7983_441+7997d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142432 | |||||||
| chr2:85142432 | ATGTGTGT others(9): Show |
A | 165 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(162): Show |
165 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(162): Show |
intron_variant | MODIFIER | c.441+8000_441+8015d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | ||||||
| chr2:85142432 | ATGTGTGT others(11): Show |
A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00597.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.441+7998_441+8015d others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142432 | ||||||
| chr2:85142433 | TGTGTGTG others(12): Show |
T | 7 | a0001c0001t0002g0067 a0002c0002t0001g0089 a0002c0002t0002g0016 others(4): Show |
7 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+7984_441+8002d others(21): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142433 | |||||||
| chr2:85142448 | G | A | 14 | a0001c0001t0001g0090 a0001c0001t0002g0167 a0002c0002t0001g0007 others(11): Show |
14 | HG00735.hp1 HG02145.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+7998G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142448 | |||||||
| chr2:85142455 | T | A | 2 | a0002c0002t0001g0057 a0002c0002t0002g0058 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.441+8005T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142455 | |||||||
| chr2:85142481 | A | AAT | 8 | a0001c0001t0001g0145 a0001c0001t0002g0067 a0002c0002t0001g0089 others(5): Show |
8 | HG01109.hp1 HG02451.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+8047_441+8048d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142481 | ||||||
| chr2:85142481 | A | AATAT | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(8): Show |
11 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.441+8045_441+8048d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85142481 | ||||||
| chr2:85142482 | A | T | 15 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(12): Show |
15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+8032A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142482 | |||||||
| chr2:85142693 | C | T | 9 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+8243C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142693 | |||||||
| chr2:85142753 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+8303T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85142753 | |||||||
| chr2:85143284 | T | C | 6 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+8834T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143284 | |||||||
| chr2:85143442 | TA | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+8994delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85143442 | ||||||
| chr2:85143593 | C | T | 1 | a0002c0002t0001g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.441+9143C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143593 | |||||||
| chr2:85143645 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.441+9195G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143645 | |||||||
| chr2:85143696 | G | A | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+9246G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143696 | |||||||
| chr2:85143790 | T | C | 18 | a0001c0001t0001g0090 a0001c0001t0001g0161 a0001c0001t0001g0163 others(15): Show |
18 | HG00735.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+9340T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85143790 | |||||||
| chr2:85144047 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.441+9597G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144047 | |||||||
| chr2:85144103 | A | G | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.441+9653A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144103 | |||||||
| chr2:85144178 | T | C | 9 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0040 others(6): Show |
9 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+9728T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144178 | |||||||
| chr2:85144417 | C | CA | 9 | a0001c0001t0001g0212 a0001c0001t0005g0001 a0002c0002t0001g0024 others(6): Show |
9 | HG00741.hp1 HG01261.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+9984dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144417 | ||||||
| chr2:85144417 | C | CAA | 11 | a0001c0001t0001g0099 a0001c0001t0002g0067 a0001c0001t0002g0100 others(8): Show |
11 | HG01071.hp2 HG01884.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+9983_441+9984d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144417 | ||||||
| chr2:85144417 | CA | C | 136 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(133): Show |
136 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.441+9984delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144417 | ||||||
| chr2:85144435 | C | A | 31 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0170 others(28): Show |
31 | HG01071.hp2 HG01175.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+9985C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144435 | |||||||
| chr2:85144611 | A | T | 5 | a0001c0001t0001g0099 a0001c0001t0002g0100 a0002c0002t0001g0087 others(2): Show |
5 | HG03139.hp1 HG03139.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+10161A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144611 | |||||||
| chr2:85144705 | TTC | T | 77 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0091 others(74): Show |
77 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.441+10269_441+1027 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144705 | ||||||
| chr2:85144705 | TTCTC | T | 21 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0107 others(18): Show |
21 | HG00597.hp1 HG00639.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+10267_441+1027 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144705 | ||||||
| chr2:85144705 | TTCTCTC | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG00735.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+10265_441+1027 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144705 | ||||||
| chr2:85144713 | C | G | 2 | a0001c0001t0001g0180 a0002c0002t0001g0056 |
2 | NA18951.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.441+10263C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144713 | |||||||
| chr2:85144715 | C | G | 28 | a0001c0001t0001g0097 a0001c0001t0001g0133 a0001c0001t0001g0136 others(25): Show |
28 | HG01106.hp2 HG01167.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+10265C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144715 | |||||||
| chr2:85144717 | C | G | 98 | a0001c0001t0001g0015 a0001c0001t0001g0091 a0001c0001t0001g0097 others(95): Show |
98 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.441+10267C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144717 | |||||||
| chr2:85144719 | C | CTCTCTG | 4 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0045 others(1): Show |
4 | HG01071.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+10270_441+1027 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | ||||||
| chr2:85144719 | C | CTCTCTGT others(1): Show |
5 | a0002c0002t0001g0040 a0002c0002t0001g0042 a0002c0002t0002g0043 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+10270_441+1027 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | ||||||
| chr2:85144719 | C | CTG | 13 | a0001c0001t0001g0031 a0001c0001t0001g0229 a0001c0001t0001g0230 others(10): Show |
13 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+10299_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | ||||||
| chr2:85144719 | C | G | 130 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(127): Show |
130 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.441+10269C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144719 | |||||||
| chr2:85144719 | CTG | C | 2 | a0001c0001t0001g0213 a0002c0002t0003g0084 |
2 | HG01071.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.441+10299_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144719 | ||||||
| chr2:85144721 | G | C | 10 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0002g0100 others(7): Show |
10 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+10271G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144721 | |||||||
| chr2:85144723 | G | C | 6 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+10273G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144723 | |||||||
| chr2:85144749 | G | GTGTGTGT others(1): Show |
6 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(3): Show |
6 | HG02257.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+10300_441+1030 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | ||||||
| chr2:85144749 | G | GTGTGTT | 2 | a0002c0002t0002g0061 a0002c0002t0002g0066 |
2 | HG00735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.441+10300_441+1030 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | ||||||
| chr2:85144749 | G | GTGTT | 16 | a0001c0001t0001g0090 a0001c0001t0001g0136 a0002c0002t0001g0007 others(13): Show |
16 | HG01109.hp1 HG02145.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+10300_441+1030 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | ||||||
| chr2:85144749 | G | GTT | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG01891.hp2 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+10300_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | ||||||
| chr2:85144749 | G | T | 112 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0091 others(109): Show |
112 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.441+10299G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144749 | |||||||
| chr2:85144749 | GTA | G | 3 | a0001c0001t0001g0099 a0001c0001t0002g0100 a0002c0002t0001g0087 |
3 | HG03139.hp2 HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+10301_441+1030 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85144749 | ||||||
| chr2:85144751 | A | G | 159 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(156): Show |
159 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.441+10301A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144751 | |||||||
| chr2:85144806 | G | A | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+10356G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144806 | |||||||
| chr2:85144816 | G | A | 3 | a0001c0001t0005g0001 a0001c0001t0005g0002 a0001c0001t0006g0003 |
3 | HG01261.hp2 HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.441+10366G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144816 | |||||||
| chr2:85144854 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.441+10404C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144854 | |||||||
| chr2:85144971 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(139): Show |
142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+10521G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144971 | |||||||
| chr2:85144978 | G | A | 18 | a0001c0001t0001g0090 a0001c0001t0001g0161 a0001c0001t0001g0163 others(15): Show |
18 | HG00735.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+10528G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85144978 | |||||||
| chr2:85145016 | C | T | 124 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0091 others(121): Show |
124 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.441+10566C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145016 | |||||||
| chr2:85145107 | C | T | 12 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0001c0001t0002g0147 others(9): Show |
12 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+10657C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145107 | |||||||
| chr2:85145251 | T | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0232 a0001c0001t0001g0234 others(2): Show |
5 | HG02630.hp2 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+10801T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145251 | |||||||
| chr2:85145410 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+10960A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145410 | |||||||
| chr2:85145499 | C | G | 1 | a0002c0002t0004g0055 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.441+11049C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145499 | |||||||
| chr2:85145546 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0228 |
2 | HG00280.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.441+11096G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145546 | |||||||
| chr2:85145582 | G | A | 4 | a0001c0001t0001g0099 a0001c0001t0002g0100 a0002c0002t0001g0087 others(1): Show |
4 | HG03139.hp2 HG03669.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+11132G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145582 | |||||||
| chr2:85145615 | G | A | 1 | a0002c0002t0001g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.441+11165G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145615 | |||||||
| chr2:85145884 | A | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+11434A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85145884 | |||||||
| chr2:85146054 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.441+11604C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146054 | |||||||
| chr2:85146492 | T | C | 15 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(12): Show |
15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+12042T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146492 | |||||||
| chr2:85146497 | C | CT | 9 | a0001c0001t0001g0088 a0001c0001t0001g0170 a0001c0001t0001g0171 others(6): Show |
9 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+12068dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85146497 | ||||||
| chr2:85146497 | CT | C | 24 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0002g0100 others(21): Show |
24 | HG00741.hp1 HG01071.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+12068delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85146497 | ||||||
| chr2:85146497 | CTTT | C | 135 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(132): Show |
135 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.441+12066_441+1206 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85146497 | ||||||
| chr2:85146501 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.441+12051T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146501 | |||||||
| chr2:85146626 | T | C | 176 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(173): Show |
176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+12176T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146626 | |||||||
| chr2:85146694 | A | G | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(142): Show |
145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+12244A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146694 | |||||||
| chr2:85146704 | G | A | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+12254G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146704 | |||||||
| chr2:85146730 | C | T | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.441+12280C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146730 | |||||||
| chr2:85146753 | G | A | 4 | a0001c0001t0002g0105 a0002c0002t0001g0032 a0002c0002t0001g0033 others(1): Show |
4 | HG02818.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+12303G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146753 | |||||||
| chr2:85146755 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.441+12305C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146755 | |||||||
| chr2:85146775 | A | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441+12325A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146775 | |||||||
| chr2:85146853 | C | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+12403C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85146853 | |||||||
| chr2:85147038 | T | G | 3 | a0001c0001t0005g0001 a0001c0001t0005g0002 a0001c0001t0006g0003 |
3 | HG01261.hp2 HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.441+12588T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147038 | |||||||
| chr2:85147074 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(139): Show |
142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+12624G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147074 | |||||||
| chr2:85147138 | GATAA | G | 12 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0001c0001t0002g0147 others(9): Show |
12 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+12694_441+1269 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85147138 | ||||||
| chr2:85147192 | A | C | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(142): Show |
145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+12742A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147192 | |||||||
| chr2:85147288 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.441+12838G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147288 | |||||||
| chr2:85147294 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(139): Show |
142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+12844G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147294 | |||||||
| chr2:85147357 | C | T | 173 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(170): Show |
173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+12907C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147357 | |||||||
| chr2:85147359 | A | G | 173 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(170): Show |
173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+12909A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147359 | |||||||
| chr2:85147403 | A | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(139): Show |
142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+12953A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147403 | |||||||
| chr2:85147558 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.441+13108G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147558 | |||||||
| chr2:85147655 | C | T | 27 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0148 others(24): Show |
27 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.441+13205C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147655 | |||||||
| chr2:85147692 | C | G | 1 | a0010c0011t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.441+13242C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147692 | |||||||
| chr2:85147700 | C | T | 5 | a0002c0002t0001g0089 a0002c0002t0002g0016 a0002c0002t0002g0018 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+13250C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147700 | |||||||
| chr2:85147878 | T | C | 176 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(173): Show |
176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+13428T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147878 | |||||||
| chr2:85147891 | C | T | 1 | a0002c0002t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+13441C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85147891 | |||||||
| chr2:85148009 | T | G | 176 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(173): Show |
176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+13559T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148009 | |||||||
| chr2:85148068 | T | G | 3 | a0001c0001t0001g0213 a0002c0002t0002g0063 a0006c0017t0001g0215 |
3 | HG01071.hp1 HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.441+13618T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148068 | |||||||
| chr2:85148159 | G | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0002g0067 others(18): Show |
21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+13709G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148159 | |||||||
| chr2:85148216 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+13766G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148216 | |||||||
| chr2:85148451 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(139): Show |
142 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.441+14001G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148451 | |||||||
| chr2:85148473 | A | T | 3 | a0001c0001t0002g0129 a0002c0002t0002g0020 a0002c0002t0002g0054 |
3 | HG01074.hp2 HG02145.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.441+14023A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148473 | |||||||
| chr2:85148553 | C | T | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0002g0067 others(18): Show |
21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+14103C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148553 | |||||||
| chr2:85148771 | A | AT | 113 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(110): Show |
113 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.441+14341dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85148771 | ||||||
| chr2:85148771 | A | ATTT | 10 | a0001c0001t0001g0099 a0001c0001t0001g0170 a0001c0001t0001g0171 others(7): Show |
10 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+14339_441+1434 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85148771 | ||||||
| chr2:85148771 | AT | A | 7 | a0001c0001t0001g0149 a0001c0001t0006g0005 a0002c0002t0001g0037 others(4): Show |
7 | HG00639.hp1 HG01109.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+14341delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85148771 | ||||||
| chr2:85148923 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+14473C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148923 | |||||||
| chr2:85148998 | T | C | 176 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(173): Show |
176 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(173): Show |
intron_variant | MODIFIER | c.441+14548T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85148998 | |||||||
| chr2:85149071 | G | A | 15 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(12): Show |
15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+14621G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149071 | |||||||
| chr2:85149109 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.441+14659A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149109 | |||||||
| chr2:85149283 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.441+14833A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149283 | |||||||
| chr2:85149303 | A | ATATATGT others(25): Show |
6 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+14861_441+1489 others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149303 | ||||||
| chr2:85149326 | C | CAT | 140 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(137): Show |
140 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.441+14879_441+1488 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149326 | ||||||
| chr2:85149346 | T | TAC | 20 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0002g0067 others(17): Show |
20 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.441+14907_441+1490 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149346 | ||||||
| chr2:85149346 | T | TACACAC | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+14903_441+1490 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149346 | ||||||
| chr2:85149548 | TAG | T | 2 | a0001c0001t0001g0226 a0008c0015t0001g0227 |
2 | HG02165.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.441+15101_441+1510 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85149548 | ||||||
| chr2:85149692 | T | C | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+15242T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149692 | |||||||
| chr2:85149804 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+15354C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149804 | |||||||
| chr2:85149817 | G | A | 2 | a0002c0002t0001g0022 a0002c0002t0001g0023 |
2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.441+15367G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149817 | |||||||
| chr2:85149827 | G | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+15377G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149827 | |||||||
| chr2:85149847 | T | C | 7 | a0001c0001t0002g0147 a0001c0001t0002g0181 a0001c0001t0005g0004 others(4): Show |
7 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+15397T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149847 | |||||||
| chr2:85149947 | G | A | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+15497G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85149947 | |||||||
| chr2:85150056 | T | C | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0002g0067 others(18): Show |
21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+15606T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150056 | |||||||
| chr2:85150315 | C | G | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+15865C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150315 | |||||||
| chr2:85150357 | C | A | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+15907C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150357 | |||||||
| chr2:85150382 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.441+15932C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150382 | |||||||
| chr2:85150453 | C | T | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(142): Show |
145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+16003C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150453 | |||||||
| chr2:85150502 | T | G | 3 | a0001c0001t0001g0199 a0002c0002t0002g0048 a0002c0002t0004g0055 |
3 | HG02056.hp2 HG02083.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.441+16052T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150502 | |||||||
| chr2:85150586 | C | CT | 18 | a0001c0001t0001g0099 a0001c0001t0001g0128 a0001c0001t0002g0100 others(15): Show |
18 | HG00738.hp2 HG01074.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+16150dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85150586 | ||||||
| chr2:85150586 | CT | C | 5 | a0001c0001t0001g0150 a0001c0001t0001g0156 a0002c0002t0002g0016 others(2): Show |
5 | HG01952.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+16150delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85150586 | ||||||
| chr2:85150673 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.441+16223C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150673 | |||||||
| chr2:85150687 | T | C | 26 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0148 others(23): Show |
26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+16237T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150687 | |||||||
| chr2:85150751 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+16301T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150751 | |||||||
| chr2:85150856 | A | G | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(142): Show |
145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+16406A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150856 | |||||||
| chr2:85150901 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+16451C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150901 | |||||||
| chr2:85150971 | C | T | 1 | a0002c0002t0002g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.441+16521C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85150971 | |||||||
| chr2:85151028 | T | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0002g0067 others(18): Show |
21 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+16578T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151028 | |||||||
| chr2:85151125 | T | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+16675T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151125 | |||||||
| chr2:85151172 | C | T | 15 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(12): Show |
15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+16722C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151172 | |||||||
| chr2:85151540 | T | A | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(142): Show |
145 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.441+17090T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151540 | |||||||
| chr2:85151543 | C | A | 6 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+17093C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151543 | |||||||
| chr2:85151698 | C | G | 173 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(170): Show |
173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+17248C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151698 | |||||||
| chr2:85151771 | C | A | 119 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(116): Show |
119 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.441+17321C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151771 | |||||||
| chr2:85151779 | G | T | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+17329G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85151779 | |||||||
| chr2:85152234 | C | G | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+17784C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152234 | |||||||
| chr2:85152435 | C | CT | 107 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0091 others(104): Show |
107 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.441+17986dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152435 | ||||||
| chr2:85152435 | C | CTT | 53 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0095 others(50): Show |
53 | HG00597.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.441+17986_441+1798 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152435 | ||||||
| chr2:85152435 | C | CTTT | 10 | a0001c0001t0001g0099 a0001c0001t0001g0171 a0001c0001t0002g0100 others(7): Show |
10 | HG01175.hp2 HG01258.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+17986_441+1798 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152435 | ||||||
| chr2:85152437 | C | T | 173 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(170): Show |
173 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(170): Show |
intron_variant | MODIFIER | c.441+17987C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152437 | |||||||
| chr2:85152476 | C | T | 26 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0148 others(23): Show |
26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+18026C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152476 | |||||||
| chr2:85152495 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.441+18045C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152495 | |||||||
| chr2:85152533 | C | G | 163 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(160): Show |
163 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.441+18083C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152533 | |||||||
| chr2:85152606 | C | T | 52 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0096 others(49): Show |
52 | HG00597.hp1 HG00639.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.441+18156C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152606 | |||||||
| chr2:85152649 | GGTCTTAA others(80): Show |
G | 26 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0148 others(23): Show |
26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+18204_441+1829 others(91): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85152649 | ||||||
| chr2:85152669 | G | A | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+18219G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152669 | |||||||
| chr2:85152768 | G | A | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+18318G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152768 | |||||||
| chr2:85152791 | T | C | 150 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(147): Show |
150 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.441+18341T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152791 | |||||||
| chr2:85152881 | T | C | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+18431T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152881 | |||||||
| chr2:85152929 | T | C | 26 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0148 others(23): Show |
26 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.441+18479T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85152929 | |||||||
| chr2:85153016 | A | G | 6 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+18566A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153016 | |||||||
| chr2:85153070 | C | T | 2 | a0002c0002t0001g0087 a0004c0012t0002g0184 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+18620C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153070 | |||||||
| chr2:85153157 | T | A | 1 | a0002c0002t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.441+18707T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153157 | |||||||
| chr2:85153339 | A | C | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+18889A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153339 | |||||||
| chr2:85153340 | A | AT | 6 | a0001c0001t0001g0076 a0001c0001t0001g0160 a0002c0002t0001g0013 others(3): Show |
6 | HG01257.hp1 HG02486.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+18909dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATATTTTT others(24): Show |
1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.441+18891_441+1889 others(35): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATATTTTT others(25): Show |
2 | a0002c0002t0001g0007 a0002c0002t0002g0008 |
2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.441+18891_441+1889 others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATATTTTT others(26): Show |
1 | a0002c0002t0001g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.441+18891_441+1889 others(37): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATGTTTTT others(11): Show |
3 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+18891_441+1889 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATGTTTTT others(12): Show |
3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 |
3 | HG01256.hp2 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.441+18891_441+1889 others(23): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATGTTTTT others(13): Show |
1 | a0002c0002t0001g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.441+18891_441+1889 others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTT | 32 | a0001c0001t0001g0014 a0001c0001t0001g0111 a0001c0001t0001g0112 others(29): Show |
32 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+18905_441+1890 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTT | 59 | a0001c0001t0001g0015 a0001c0001t0001g0091 a0001c0001t0001g0097 others(56): Show |
59 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.441+18904_441+1890 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT | 6 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0187 others(3): Show |
6 | HG01346.hp2 HG02056.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+18903_441+1890 others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0099 a0001c0001t0001g0211 a0001c0001t0002g0100 others(1): Show |
4 | HG03540.hp2 HG03669.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+18900_441+1890 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(4): Show |
24 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0148 others(21): Show |
24 | HG00597.hp1 HG00639.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+18899_441+1890 others(15): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+18898_441+1890 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(6): Show |
13 | a0001c0001t0005g0001 a0001c0001t0005g0002 a0001c0001t0006g0003 others(10): Show |
13 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+18897_441+1890 others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0208 a0002c0002t0002g0039 |
3 | HG03041.hp1 HG03209.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.441+18896_441+1890 others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0161 a0001c0001t0002g0162 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.441+18895_441+1890 others(19): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0163 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.441+18894_441+1890 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(10): Show |
1 | a0002c0002t0001g0069 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.441+18893_441+1890 others(21): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(11): Show |
1 | a0002c0002t0001g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.441+18892_441+1890 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(17): Show |
1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441+18909_441+1891 others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(18): Show |
5 | a0001c0001t0001g0090 a0002c0002t0001g0012 a0002c0002t0001g0062 others(2): Show |
5 | HG00735.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+18909_441+1891 others(29): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | A | ATTTTTTT others(19): Show |
1 | a0002c0002t0002g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.441+18909_441+1891 others(30): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153340 | AT | A | 5 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0002c0002t0001g0087 others(2): Show |
5 | HG02572.hp2 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+18909delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85153340 | ||||||
| chr2:85153381 | A | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+18931A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153381 | |||||||
| chr2:85153514 | T | G | 8 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
8 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+19064T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153514 | |||||||
| chr2:85153543 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0234 a0005c0006t0010g0233 |
3 | HG02723.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.441+19093G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153543 | |||||||
| chr2:85153621 | G | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
5 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+19171G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153621 | |||||||
| chr2:85153630 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+19180T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153630 | |||||||
| chr2:85153724 | A | T | 1 | a0001c0001t0002g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+19274A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153724 | |||||||
| chr2:85153953 | G | A | 15 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(12): Show |
15 | HG01071.hp2 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+19503G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85153953 | |||||||
| chr2:85154134 | A | G | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+19684A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154134 | |||||||
| chr2:85154147 | C | T | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+19697C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154147 | |||||||
| chr2:85154192 | G | A | 3 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+19742G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154192 | |||||||
| chr2:85154293 | T | C | 10 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0001c0001t0002g0147 others(7): Show |
10 | HG00639.hp1 HG00738.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+19843T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154293 | |||||||
| chr2:85154344 | A | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+19894A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154344 | |||||||
| chr2:85154533 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0225 a0001c0001t0001g0228 |
3 | HG00280.hp1 HG01358.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.441+20083C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154533 | |||||||
| chr2:85154737 | C | T | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.441+20287C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154737 | |||||||
| chr2:85154768 | A | G | 7 | a0001c0001t0001g0088 a0002c0002t0001g0089 a0002c0002t0002g0016 others(4): Show |
7 | HG01109.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+20318A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154768 | |||||||
| chr2:85154823 | C | CT | 6 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+20386dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85154823 | ||||||
| chr2:85154871 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+20421C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154871 | |||||||
| chr2:85154888 | C | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+20438C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154888 | |||||||
| chr2:85154970 | C | A | 2 | a0001c0001t0007g0134 a0004c0005t0001g0135 |
2 | HG01256.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.441+20520C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85154970 | |||||||
| chr2:85155009 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.441+20559G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155009 | |||||||
| chr2:85155177 | C | T | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441+20727C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155177 | |||||||
| chr2:85155236 | G | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.441+20786G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155236 | |||||||
| chr2:85155291 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+20841A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155291 | |||||||
| chr2:85155325 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+20875C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155325 | |||||||
| chr2:85155346 | C | A | 19 | a0001c0001t0001g0090 a0001c0001t0001g0161 a0001c0001t0001g0163 others(16): Show |
19 | HG00735.hp1 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.441+20896C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155346 | |||||||
| chr2:85155350 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.441+20900G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155350 | |||||||
| chr2:85155388 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.441+20938A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155388 | |||||||
| chr2:85155607 | A | T | 120 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(117): Show |
120 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.441+21157A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155607 | |||||||
| chr2:85155910 | G | T | 1 | a0004c0005t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441+21460G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155910 | |||||||
| chr2:85155911 | G | T | 1 | a0004c0005t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441+21461G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85155911 | |||||||
| chr2:85156002 | A | T | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+21552A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156002 | |||||||
| chr2:85156015 | G | A | 2 | a0002c0002t0001g0057 a0002c0002t0002g0058 |
2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.441+21565G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156015 | |||||||
| chr2:85156065 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441+21615A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156065 | |||||||
| chr2:85156318 | T | G | 5 | a0002c0002t0001g0089 a0002c0002t0002g0016 a0002c0002t0002g0018 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+21868T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156318 | |||||||
| chr2:85156562 | T | C | 2 | a0002c0002t0001g0022 a0002c0002t0001g0023 |
2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.441+22112T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156562 | |||||||
| chr2:85156661 | T | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0001g0229 others(4): Show |
7 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+22211T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156661 | |||||||
| chr2:85156782 | C | T | 2 | a0002c0002t0001g0062 a0002c0002t0002g0061 |
2 | HG00735.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.441+22332C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156782 | |||||||
| chr2:85156790 | T | C | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+22340T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85156790 | |||||||
| chr2:85156867 | GATATTTT others(8): Show |
G | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+22447_441+2246 others(19): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85156867 | ||||||
| chr2:85157056 | C | T | 19 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0148 others(16): Show |
19 | HG00597.hp1 HG00639.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+22606C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157056 | |||||||
| chr2:85157245 | G | T | 1 | a0007c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.441+22795G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157245 | |||||||
| chr2:85157264 | C | A | 1 | a0002c0002t0001g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.441+22814C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157264 | |||||||
| chr2:85157629 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.441+23179A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157629 | |||||||
| chr2:85157830 | C | A | 2 | a0001c0001t0002g0102 a0003c0004t0002g0114 |
2 | HG01346.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.441+23380C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157830 | |||||||
| chr2:85157868 | C | G | 7 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0040 others(4): Show |
7 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+23418C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157868 | |||||||
| chr2:85157893 | C | T | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+23443C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157893 | |||||||
| chr2:85157929 | T | C | 28 | a0001c0001t0001g0090 a0001c0001t0001g0161 a0001c0001t0001g0163 others(25): Show |
28 | HG00735.hp1 HG01071.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.441+23479T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157929 | |||||||
| chr2:85157994 | G | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
5 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+23544G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85157994 | |||||||
| chr2:85158272 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.441+23822C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158272 | |||||||
| chr2:85158315 | C | T | 6 | a0001c0001t0001g0092 a0001c0001t0005g0001 a0001c0001t0005g0002 others(3): Show |
6 | HG01257.hp2 HG01258.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+23865C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158315 | |||||||
| chr2:85158345 | T | A | 5 | a0002c0002t0001g0089 a0002c0002t0002g0016 a0002c0002t0002g0018 others(2): Show |
5 | HG01109.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+23895T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158345 | |||||||
| chr2:85158349 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.441+23899G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158349 | |||||||
| chr2:85158580 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+24130T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158580 | |||||||
| chr2:85158672 | G | A | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.441+24222G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158672 | |||||||
| chr2:85158735 | G | A | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+24285G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85158735 | |||||||
| chr2:85159045 | G | A | 1 | a0003c0004t0002g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.441+24595G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85159045 | |||||||
| chr2:85159638 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+25188A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85159638 | |||||||
| chr2:85160046 | C | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02257.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+25596C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160046 | |||||||
| chr2:85160347 | C | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+25897C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160347 | |||||||
| chr2:85160370 | A | G | 133 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(130): Show |
133 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.441+25920A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160370 | |||||||
| chr2:85160382 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+25932G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160382 | |||||||
| chr2:85160628 | G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+26178G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160628 | |||||||
| chr2:85160676 | G | A | 2 | a0002c0003t0002g0086 a0004c0012t0002g0184 |
2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.441+26226G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160676 | |||||||
| chr2:85160829 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+26379G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160829 | |||||||
| chr2:85160901 | GCA | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+26452_441+2645 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160901 | |||||||
| chr2:85160906 | C | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+26456C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160906 | |||||||
| chr2:85160911 | A | G | 2 | a0001c0001t0002g0100 a0002c0002t0002g0017 |
2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+26461A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85160911 | |||||||
| chr2:85161061 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441+26611C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161061 | |||||||
| chr2:85161062 | C | T | 1 | a0002c0002t0001g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.441+26612C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161062 | |||||||
| chr2:85161063 | G | A | 12 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0187 others(9): Show |
12 | HG00621.hp1 HG02080.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+26613G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161063 | |||||||
| chr2:85161134 | C | G | 23 | a0001c0001t0001g0031 a0001c0001t0001g0126 a0001c0001t0001g0139 others(20): Show |
23 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.441+26684C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161134 | |||||||
| chr2:85161185 | G | A | 2 | a0001c0001t0001g0112 a0002c0002t0003g0083 |
2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.441+26735G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161185 | |||||||
| chr2:85161221 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441+26771A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161221 | |||||||
| chr2:85161233 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+26783A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161233 | |||||||
| chr2:85161359 | G | C | 1 | a0001c0001t0007g0134 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.441+26909G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161359 | |||||||
| chr2:85161444 | G | T | 1 | a0001c0001t0002g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.441+26994G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161444 | |||||||
| chr2:85161625 | C | A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0126 a0001c0001t0001g0139 others(19): Show |
22 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.441+27175C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161625 | |||||||
| chr2:85161870 | C | T | 11 | a0001c0001t0001g0160 a0001c0001t0001g0197 a0001c0001t0001g0221 others(8): Show |
11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+27420C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161870 | |||||||
| chr2:85161891 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+27441C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161891 | |||||||
| chr2:85161907 | G | C | 2 | a0001c0001t0001g0112 a0002c0002t0003g0083 |
2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.441+27457G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85161907 | |||||||
| chr2:85162045 | A | G | 36 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(33): Show |
36 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+27595A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162045 | |||||||
| chr2:85162057 | T | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+27607T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162057 | |||||||
| chr2:85162062 | A | G | 11 | a0001c0001t0001g0160 a0001c0001t0001g0197 a0001c0001t0001g0221 others(8): Show |
11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+27612A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162062 | |||||||
| chr2:85162073 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.441+27623A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162073 | |||||||
| chr2:85162111 | T | C | 2 | a0001c0001t0002g0100 a0002c0002t0002g0017 |
2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+27661T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162111 | |||||||
| chr2:85162174 | G | T | 1 | a0001c0001t0006g0005 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.441+27724G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162174 | |||||||
| chr2:85162182 | G | C | 34 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(31): Show |
34 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+27732G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162182 | |||||||
| chr2:85162282 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441+27832C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162282 | |||||||
| chr2:85162489 | C | T | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.441+28039C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162489 | |||||||
| chr2:85162562 | T | C | 36 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(33): Show |
36 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+28112T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162562 | |||||||
| chr2:85162568 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+28118A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162568 | |||||||
| chr2:85162572 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.441+28122T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162572 | |||||||
| chr2:85162582 | C | T | 11 | a0001c0001t0001g0160 a0001c0001t0001g0197 a0001c0001t0001g0221 others(8): Show |
11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+28132C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162582 | |||||||
| chr2:85162591 | T | A | 11 | a0001c0001t0001g0160 a0001c0001t0001g0197 a0001c0001t0001g0221 others(8): Show |
11 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+28141T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162591 | |||||||
| chr2:85162653 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.441+28203C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162653 | |||||||
| chr2:85162667 | G | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+28217G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162667 | |||||||
| chr2:85162717 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+28267C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162717 | |||||||
| chr2:85162852 | T | C | 34 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(31): Show |
34 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+28402T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162852 | |||||||
| chr2:85162918 | C | A | 39 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(36): Show |
39 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.441+28468C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162918 | |||||||
| chr2:85162963 | A | C | 2 | a0001c0001t0001g0197 a0001c0001t0002g0196 |
2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.441+28513A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85162963 | |||||||
| chr2:85163042 | G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+28592G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163042 | |||||||
| chr2:85163080 | G | A | 1 | a0002c0003t0002g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441+28630G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163080 | |||||||
| chr2:85163318 | C | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0131 others(11): Show |
14 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+28868C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163318 | |||||||
| chr2:85163631 | G | C | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+29181G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163631 | |||||||
| chr2:85163659 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+29209G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163659 | |||||||
| chr2:85163709 | G | A | 2 | a0001c0001t0002g0100 a0002c0002t0002g0017 |
2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+29259G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163709 | |||||||
| chr2:85163774 | TA | T | 2 | a0002c0003t0002g0036 a0002c0007t0002g0029 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.441+29325delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163774 | |||||||
| chr2:85163952 | T | C | 1 | a0002c0002t0003g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.441+29502T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85163952 | |||||||
| chr2:85164132 | C | T | 46 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0096 others(43): Show |
46 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.441+29682C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164132 | |||||||
| chr2:85164163 | C | T | 2 | a0001c0001t0001g0213 a0006c0017t0001g0215 |
2 | HG01071.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.441+29713C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164163 | |||||||
| chr2:85164185 | G | A | 39 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(36): Show |
39 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.441+29735G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164185 | |||||||
| chr2:85164252 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0002g0132 a0002c0002t0001g0093 others(2): Show |
5 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+29802G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164252 | |||||||
| chr2:85164344 | G | A | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.441+29894G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164344 | |||||||
| chr2:85164441 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+29991G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164441 | |||||||
| chr2:85164622 | A | T | 12 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0197 others(9): Show |
12 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+30172A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164622 | |||||||
| chr2:85164752 | G | A | 36 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(33): Show |
36 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.441+30302G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164752 | |||||||
| chr2:85164886 | T | C | 41 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(38): Show |
41 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.441+30436T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164886 | |||||||
| chr2:85164970 | A | T | 153 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0091 others(150): Show |
153 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.441+30520A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164970 | |||||||
| chr2:85164988 | T | C | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+30538T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85164988 | |||||||
| chr2:85165032 | A | C | 4 | a0001c0001t0001g0031 a0002c0002t0001g0030 a0002c0002t0001g0032 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+30582A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165032 | |||||||
| chr2:85165036 | G | C | 4 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0007g0134 others(1): Show |
4 | HG01256.hp1 HG02165.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+30586G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165036 | |||||||
| chr2:85165076 | C | T | 31 | a0001c0001t0001g0031 a0001c0001t0001g0092 a0001c0001t0001g0126 others(28): Show |
31 | HG01175.hp2 HG01243.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+30626C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165076 | |||||||
| chr2:85165093 | T | G | 78 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0092 others(75): Show |
78 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.441+30643T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165093 | |||||||
| chr2:85165362 | AACAAGC | A | 30 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0124 others(27): Show |
30 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+30913_441+3091 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165362 | |||||||
| chr2:85165369 | C | T | 30 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0124 others(27): Show |
30 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+30919C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165369 | |||||||
| chr2:85165371 | A | T | 30 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0124 others(27): Show |
30 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+30921A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165371 | |||||||
| chr2:85165424 | T | C | 10 | a0001c0001t0001g0092 a0001c0001t0001g0229 a0001c0001t0001g0230 others(7): Show |
10 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+30974T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165424 | |||||||
| chr2:85165852 | A | G | 12 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0197 others(9): Show |
12 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+31402A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165852 | |||||||
| chr2:85165882 | A | G | 14 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(11): Show |
14 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+31432A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165882 | |||||||
| chr2:85165972 | T | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.441+31522T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85165972 | |||||||
| chr2:85166027 | T | G | 1 | a0002c0002t0001g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.441+31577T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166027 | |||||||
| chr2:85166541 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441+32091G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166541 | |||||||
| chr2:85166564 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+32114C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166564 | |||||||
| chr2:85166638 | A | G | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+32188A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166638 | |||||||
| chr2:85166668 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+32218C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166668 | |||||||
| chr2:85166861 | G | C | 12 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0197 others(9): Show |
12 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+32411G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166861 | |||||||
| chr2:85166869 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.441+32419T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166869 | |||||||
| chr2:85166882 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+32432C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166882 | |||||||
| chr2:85166959 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0166 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+32509C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166959 | |||||||
| chr2:85166988 | T | C | 4 | a0001c0001t0001g0092 a0001c0001t0002g0132 a0002c0002t0001g0093 others(1): Show |
4 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+32538T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166988 | |||||||
| chr2:85166991 | T | C | 88 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(85): Show |
88 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.441+32541T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85166991 | |||||||
| chr2:85167023 | C | T | 11 | a0001c0001t0001g0076 a0001c0001t0001g0183 a0001c0001t0001g0213 others(8): Show |
11 | HG00280.hp2 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+32573C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167023 | |||||||
| chr2:85167139 | T | G | 18 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(15): Show |
18 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+32689T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167139 | |||||||
| chr2:85167168 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0228 a0002c0002t0001g0026 |
3 | HG00280.hp1 HG01358.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.441+32718C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167168 | |||||||
| chr2:85167319 | A | G | 13 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+32869A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167319 | |||||||
| chr2:85167351 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.441+32901T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167351 | |||||||
| chr2:85167414 | T | A | 2 | a0001c0001t0001g0119 a0002c0002t0001g0025 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.441+32964T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167414 | |||||||
| chr2:85167449 | C | G | 27 | a0001c0001t0001g0092 a0001c0001t0001g0145 a0001c0001t0001g0160 others(24): Show |
27 | HG00735.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.441+32999C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167449 | |||||||
| chr2:85167488 | A | G | 66 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(63): Show |
66 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.441+33038A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167488 | |||||||
| chr2:85167506 | C | T | 1 | a0008c0015t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441+33056C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167506 | |||||||
| chr2:85167981 | C | T | 48 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(45): Show |
48 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.441+33531C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85167981 | |||||||
| chr2:85168047 | A | G | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33597A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168047 | |||||||
| chr2:85168068 | TAA | T | 16 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(13): Show |
16 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+33620_441+3362 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168068 | ||||||
| chr2:85168082 | T | A | 1 | a0001c0001t0006g0005 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.441+33632T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168082 | |||||||
| chr2:85168192 | A | AAC | 18 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(15): Show |
18 | HG01515.hp1 HG02257.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+33772_441+3377 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACAC | 5 | a0001c0001t0001g0031 a0001c0001t0002g0098 a0002c0002t0001g0032 others(2): Show |
5 | HG02818.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+33770_441+3377 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACAC | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0002g0132 others(5): Show |
8 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+33768_441+3377 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACACA others(1): Show |
7 | a0001c0001t0001g0088 a0001c0001t0001g0108 a0001c0001t0002g0157 others(4): Show |
7 | HG00639.hp1 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+33766_441+3377 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACACA others(3): Show |
17 | a0001c0001t0001g0119 a0001c0001t0001g0160 a0001c0001t0001g0191 others(14): Show |
17 | HG01168.hp1 HG01934.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.441+33764_441+3377 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACACA others(5): Show |
19 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0130 others(16): Show |
19 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+33762_441+3377 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACACA others(7): Show |
10 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0187 others(7): Show |
10 | HG01358.hp1 HG02572.hp1 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+33760_441+3377 others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACACA others(9): Show |
2 | a0002c0007t0002g0029 a0005c0006t0002g0137 |
2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.441+33758_441+3377 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACACA others(11): Show |
8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(5): Show |
8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+33756_441+3377 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | A | AACACACA others(17): Show |
1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+33750_441+3377 others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168192 | AACAC | A | 15 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(12): Show |
15 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+33770_441+3377 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168192 | ||||||
| chr2:85168224 | A | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+33774A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168224 | |||||||
| chr2:85168234 | A | T | 73 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(70): Show |
73 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.441+33784A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168234 | |||||||
| chr2:85168378 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33928G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168378 | |||||||
| chr2:85168409 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33959C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168409 | |||||||
| chr2:85168420 | G | A | 2 | a0001c0001t0002g0100 a0002c0007t0002g0029 |
2 | HG02647.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+33970G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168420 | |||||||
| chr2:85168421 | A | C | 2 | a0001c0001t0002g0100 a0002c0007t0002g0029 |
2 | HG02647.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.441+33971A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168421 | |||||||
| chr2:85168434 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+33984G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168434 | |||||||
| chr2:85168457 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+34007C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168457 | |||||||
| chr2:85168488 | G | A | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+34038G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168488 | |||||||
| chr2:85168503 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+34053G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168503 | |||||||
| chr2:85168613 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.441+34163T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168613 | |||||||
| chr2:85168626 | CT | C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0222 a0001c0001t0002g0157 others(2): Show |
5 | HG00741.hp2 HG02622.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+34189delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85168626 | ||||||
| chr2:85168672 | A | C | 1 | a0001c0001t0002g0200 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.441+34222A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168672 | |||||||
| chr2:85168714 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+34264C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168714 | |||||||
| chr2:85168783 | G | A | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+34333G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168783 | |||||||
| chr2:85168823 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+34373A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168823 | |||||||
| chr2:85168935 | G | T | 15 | a0001c0001t0001g0160 a0001c0001t0001g0197 a0001c0001t0001g0209 others(12): Show |
15 | HG01168.hp1 HG01934.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+34485G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168935 | |||||||
| chr2:85168956 | G | A | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+34506G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85168956 | |||||||
| chr2:85169024 | A | G | 6 | a0001c0001t0001g0092 a0001c0001t0002g0132 a0001c0001t0002g0220 others(3): Show |
6 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+34574A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169024 | |||||||
| chr2:85169144 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0002g0132 a0002c0002t0001g0093 others(2): Show |
5 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+34694G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169144 | |||||||
| chr2:85169174 | C | G | 16 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(13): Show |
16 | HG02257.hp1 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+34724C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169174 | |||||||
| chr2:85169284 | C | A | 39 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(36): Show |
39 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.441+34834C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169284 | |||||||
| chr2:85169284 | C | G | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+34834C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169284 | |||||||
| chr2:85169366 | T | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+34916T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169366 | |||||||
| chr2:85169504 | T | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35054T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169504 | |||||||
| chr2:85169517 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35067A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169517 | |||||||
| chr2:85169579 | A | G | 13 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+35129A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169579 | |||||||
| chr2:85169770 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35320A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169770 | |||||||
| chr2:85169819 | G | A | 4 | a0001c0001t0001g0088 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+35369G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169819 | |||||||
| chr2:85169836 | G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35386G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169836 | |||||||
| chr2:85169884 | C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+35434C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85169884 | |||||||
| chr2:85170315 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+35865C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170315 | |||||||
| chr2:85170592 | G | A | 1 | a0008c0015t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.441+36142G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170592 | |||||||
| chr2:85170631 | T | G | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.441+36181T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170631 | |||||||
| chr2:85170877 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+36427G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170877 | |||||||
| chr2:85170934 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+36484C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85170934 | |||||||
| chr2:85171038 | G | GA | 4 | a0001c0001t0001g0088 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+36595dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85171038 | ||||||
| chr2:85171080 | G | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+36630G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171080 | |||||||
| chr2:85171124 | A | G | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+36674A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171124 | |||||||
| chr2:85171154 | G | A | 6 | a0001c0001t0001g0092 a0001c0001t0002g0098 a0001c0001t0002g0132 others(3): Show |
6 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+36704G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171154 | |||||||
| chr2:85171204 | C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+36754C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171204 | |||||||
| chr2:85171588 | A | G | 1 | a0002c0002t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.441+37138A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171588 | |||||||
| chr2:85171847 | C | T | 1 | a0002c0002t0001g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.441+37397C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171847 | |||||||
| chr2:85171928 | C | T | 1 | a0002c0002t0002g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.441+37478C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85171928 | |||||||
| chr2:85172039 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0128 |
2 | NA18961.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.441+37589A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172039 | |||||||
| chr2:85172172 | A | G | 2 | a0001c0001t0002g0100 a0003c0004t0002g0115 |
2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+37722A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172172 | |||||||
| chr2:85172173 | C | T | 81 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(78): Show |
81 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.441+37723C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172173 | |||||||
| chr2:85172193 | C | A | 12 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0131 others(9): Show |
12 | HG00597.hp2 HG00639.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+37743C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172193 | |||||||
| chr2:85172209 | A | G | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+37759A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172209 | |||||||
| chr2:85172244 | C | T | 7 | a0001c0001t0001g0088 a0001c0001t0002g0132 a0001c0001t0002g0157 others(4): Show |
7 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+37794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172244 | |||||||
| chr2:85172245 | G | A | 2 | a0001c0001t0002g0100 a0003c0004t0002g0115 |
2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+37795G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172245 | |||||||
| chr2:85172284 | A | C | 2 | a0001c0001t0001g0136 a0005c0006t0002g0137 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.441+37834A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172284 | |||||||
| chr2:85172457 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+38007C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172457 | |||||||
| chr2:85172632 | G | A | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38182G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172632 | |||||||
| chr2:85172701 | T | C | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172701 | |||||||
| chr2:85172715 | C | A | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38265C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172715 | |||||||
| chr2:85172768 | C | T | 2 | a0002c0002t0002g0016 a0002c0002t0012g0021 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.441+38318C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172768 | |||||||
| chr2:85172783 | C | G | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+38333C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172783 | |||||||
| chr2:85172902 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.441+38452C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172902 | |||||||
| chr2:85172929 | G | A | 1 | a0007c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.441+38479G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172929 | |||||||
| chr2:85172939 | G | A | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.441+38489G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172939 | |||||||
| chr2:85172974 | G | A | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.441+38524G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85172974 | |||||||
| chr2:85173038 | C | T | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+38588C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173038 | |||||||
| chr2:85173091 | C | G | 1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.441+38641C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173091 | |||||||
| chr2:85173113 | G | T | 1 | a0001c0001t0002g0200 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.441+38663G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173113 | |||||||
| chr2:85173136 | A | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+38686A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173136 | |||||||
| chr2:85173446 | T | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+38996T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173446 | |||||||
| chr2:85173449 | G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+38999G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173449 | |||||||
| chr2:85173461 | C | T | 41 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0124 others(38): Show |
41 | HG00639.hp2 HG01071.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.441+39011C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173461 | |||||||
| chr2:85173462 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+39012G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173462 | |||||||
| chr2:85173479 | G | C | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+39029G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173479 | |||||||
| chr2:85173574 | C | A | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+39124C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173574 | |||||||
| chr2:85173605 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.441+39155C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173605 | |||||||
| chr2:85173626 | G | T | 1 | a0002c0002t0004g0055 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.441+39176G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173626 | |||||||
| chr2:85173677 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+39227G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173677 | |||||||
| chr2:85173678 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+39228G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173678 | |||||||
| chr2:85173743 | C | CT | 49 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(46): Show |
49 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.441+39302dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173743 | ||||||
| chr2:85173753 | C | CTTTCTTT others(13): Show |
1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+39304_441+3930 others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173753 | ||||||
| chr2:85173753 | C | CTTTCTTT others(15): Show |
3 | a0001c0001t0001g0209 a0002c0003t0002g0086 a0004c0012t0002g0184 |
3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+39304_441+3930 others(26): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173753 | ||||||
| chr2:85173753 | C | CTTTCTTT others(16): Show |
1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441+39304_441+3930 others(27): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85173753 | ||||||
| chr2:85173797 | C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+39347C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173797 | |||||||
| chr2:85173839 | C | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+39389C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173839 | |||||||
| chr2:85173854 | G | A | 27 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(24): Show |
27 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.441+39404G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173854 | |||||||
| chr2:85173893 | C | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+39443C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173893 | |||||||
| chr2:85173977 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+39527C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173977 | |||||||
| chr2:85173982 | G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+39532G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85173982 | |||||||
| chr2:85174215 | T | C | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+39765T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174215 | |||||||
| chr2:85174228 | G | A | 4 | a0001c0001t0001g0136 a0002c0002t0001g0034 a0002c0002t0002g0018 others(1): Show |
4 | HG03209.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+39778G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174228 | |||||||
| chr2:85174465 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.441+40015G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174465 | |||||||
| chr2:85174483 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+40033A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174483 | |||||||
| chr2:85174486 | T | A | 1 | a0001c0001t0002g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+40036T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174486 | |||||||
| chr2:85174541 | A | G | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40091A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174541 | |||||||
| chr2:85174631 | T | C | 10 | a0001c0001t0001g0149 a0001c0001t0001g0199 a0001c0001t0001g0201 others(7): Show |
10 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+40181T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174631 | |||||||
| chr2:85174722 | A | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0107 others(2): Show |
5 | HG00597.hp1 NA18959.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40272A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174722 | |||||||
| chr2:85174755 | A | G | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40305A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174755 | |||||||
| chr2:85174768 | G | A | 1 | a0001c0001t0011g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.441+40318G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174768 | |||||||
| chr2:85174835 | C | T | 140 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(137): Show |
140 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.441+40385C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174835 | |||||||
| chr2:85174932 | G | A | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+40482G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174932 | |||||||
| chr2:85174983 | G | A | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+40533G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174983 | |||||||
| chr2:85174990 | G | A | 6 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0001g0042 others(3): Show |
6 | HG01071.hp2 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+40540G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85174990 | |||||||
| chr2:85175056 | C | T | 12 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+40606C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175056 | |||||||
| chr2:85175213 | C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+40763C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175213 | |||||||
| chr2:85175370 | C | T | 11 | a0001c0001t0001g0113 a0001c0001t0001g0160 a0001c0001t0001g0197 others(8): Show |
11 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+40920C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175370 | |||||||
| chr2:85175521 | G | T | 3 | a0002c0002t0001g0035 a0002c0002t0003g0073 a0002c0002t0003g0074 |
3 | HG01106.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.441+41071G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175521 | |||||||
| chr2:85175691 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+41241T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175691 | |||||||
| chr2:85175744 | G | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+41294G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175744 | |||||||
| chr2:85175851 | A | C | 76 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(73): Show |
76 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.441+41401A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175851 | |||||||
| chr2:85175927 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.441+41477G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85175927 | |||||||
| chr2:85176027 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.441+41577A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176027 | |||||||
| chr2:85176118 | T | C | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+41668T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176118 | |||||||
| chr2:85176225 | C | G | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+41775C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176225 | |||||||
| chr2:85176423 | A | G | 38 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(35): Show |
38 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.441+41973A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176423 | |||||||
| chr2:85176476 | C | T | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+42026C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176476 | |||||||
| chr2:85176510 | G | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+42060G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176510 | |||||||
| chr2:85176760 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+42310G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176760 | |||||||
| chr2:85176913 | G | A | 12 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+42463G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176913 | |||||||
| chr2:85176922 | G | A | 14 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(11): Show |
14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+42472G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176922 | |||||||
| chr2:85176962 | G | C | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+42512G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85176962 | |||||||
| chr2:85176986 | C | CA | 50 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0076 others(47): Show |
50 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.441+42559dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85176986 | ||||||
| chr2:85176986 | C | CAA | 11 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0126 others(8): Show |
11 | HG00597.hp2 HG01981.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+42558_441+4255 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85176986 | ||||||
| chr2:85176986 | CAAAAAAA | C | 12 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+42553_441+4255 others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85176986 | ||||||
| chr2:85177244 | C | T | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+42794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177244 | |||||||
| chr2:85177499 | A | G | 217 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.441+43049A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177499 | |||||||
| chr2:85177566 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.441+43116G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177566 | |||||||
| chr2:85177661 | C | T | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+43211C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177661 | |||||||
| chr2:85177760 | C | G | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+43310C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177760 | |||||||
| chr2:85177814 | A | G | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+43364A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177814 | |||||||
| chr2:85177909 | A | G | 74 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(71): Show |
74 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.441+43459A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85177909 | |||||||
| chr2:85178129 | C | T | 3 | a0001c0001t0001g0119 a0002c0002t0001g0009 a0002c0009t0001g0019 |
3 | HG02895.hp2 HG03195.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.441+43679C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85178129 | |||||||
| chr2:85178139 | G | A | 4 | a0001c0001t0001g0092 a0001c0001t0002g0132 a0002c0002t0001g0093 others(1): Show |
4 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+43689G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85178139 | |||||||
| chr2:85178246 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.441+43796G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85178246 | |||||||
| chr2:85179000 | G | A | 1 | a0003c0004t0002g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.441+44550G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179000 | |||||||
| chr2:85179103 | G | A | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+44653G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179103 | |||||||
| chr2:85179201 | G | A | 2 | a0002c0002t0001g0009 a0002c0009t0001g0019 |
2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.441+44751G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179201 | |||||||
| chr2:85179445 | T | C | 1 | a0004c0012t0002g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.441+44995T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179445 | |||||||
| chr2:85179495 | T | C | 14 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(11): Show |
14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+45045T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179495 | |||||||
| chr2:85179496 | C | T | 14 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(11): Show |
14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+45046C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179496 | |||||||
| chr2:85179726 | C | T | 5 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+45276C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179726 | |||||||
| chr2:85179737 | C | CT | 15 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(12): Show |
15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+45288dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85179737 | ||||||
| chr2:85179753 | T | A | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+45303T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85179753 | |||||||
| chr2:85180047 | G | A | 4 | a0001c0001t0001g0232 a0001c0001t0002g0067 a0002c0002t0002g0016 others(1): Show |
4 | HG02451.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+45597G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180047 | |||||||
| chr2:85180216 | T | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+45766T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180216 | |||||||
| chr2:85180222 | G | T | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+45772G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180222 | |||||||
| chr2:85180224 | T | G | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+45774T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180224 | |||||||
| chr2:85180234 | G | GT | 14 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(11): Show |
14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+45795dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85180234 | ||||||
| chr2:85180240 | T | G | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+45790T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180240 | |||||||
| chr2:85180366 | C | T | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+45916C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180366 | |||||||
| chr2:85180447 | G | A | 12 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(9): Show |
12 | HG01934.hp2 HG02056.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+45997G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180447 | |||||||
| chr2:85180549 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.441+46099A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180549 | |||||||
| chr2:85180577 | A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.441+46127A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180577 | |||||||
| chr2:85180775 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441+46325C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180775 | |||||||
| chr2:85180897 | C | T | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+46447C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180897 | |||||||
| chr2:85180961 | G | A | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+46511G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85180961 | |||||||
| chr2:85181114 | T | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.441+46664T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181114 | |||||||
| chr2:85181175 | G | A | 24 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(21): Show |
24 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+46725G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181175 | |||||||
| chr2:85181241 | G | A | 18 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(15): Show |
18 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+46791G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181241 | |||||||
| chr2:85181245 | G | C | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.441+46795G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181245 | |||||||
| chr2:85181361 | C | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+46911C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181361 | |||||||
| chr2:85181384 | A | G | 3 | a0001c0001t0001g0209 a0002c0003t0002g0086 a0004c0012t0002g0184 |
3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+46934A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181384 | |||||||
| chr2:85181428 | A | G | 92 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(89): Show |
92 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.441+46978A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181428 | |||||||
| chr2:85181700 | G | A | 1 | a0002c0002t0003g0176 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.441+47250G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181700 | |||||||
| chr2:85181843 | G | A | 24 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(21): Show |
24 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.441+47393G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181843 | |||||||
| chr2:85181937 | T | C | 15 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(12): Show |
15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+47487T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85181937 | |||||||
| chr2:85182109 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.441+47659G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182109 | |||||||
| chr2:85182116 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.441+47666G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182116 | |||||||
| chr2:85182177 | G | A | 14 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(11): Show |
14 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+47727G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182177 | |||||||
| chr2:85182236 | C | T | 15 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(12): Show |
15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+47786C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182236 | |||||||
| chr2:85182319 | G | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0097 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02165.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+47869G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182319 | |||||||
| chr2:85182388 | G | A | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+47938G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182388 | |||||||
| chr2:85182446 | C | T | 2 | a0001c0001t0001g0112 a0002c0002t0003g0083 |
2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.441+47996C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182446 | |||||||
| chr2:85182498 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.441+48048G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182498 | |||||||
| chr2:85182867 | A | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+48417A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182867 | |||||||
| chr2:85182966 | G | A | 88 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(85): Show |
88 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.441+48516G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182966 | |||||||
| chr2:85182981 | G | A | 37 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(34): Show |
37 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.441+48531G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85182981 | |||||||
| chr2:85183400 | C | G | 2 | a0001c0001t0001g0091 a0001c0001t0011g0142 |
2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.441+48950C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183400 | |||||||
| chr2:85183444 | T | C | 1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.441+48994T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183444 | |||||||
| chr2:85183509 | C | T | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+49059C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183509 | |||||||
| chr2:85183714 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.441+49264G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183714 | |||||||
| chr2:85183747 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0002g0127 others(1): Show |
4 | HG02165.hp1 NA18961.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+49297G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183747 | |||||||
| chr2:85183810 | C | T | 26 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(23): Show |
26 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.441+49360C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85183810 | |||||||
| chr2:85184047 | G | A | 1 | a0004c0005t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441+49597G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184047 | |||||||
| chr2:85184276 | C | T | 15 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(12): Show |
15 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.441+49826C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184276 | |||||||
| chr2:85184380 | G | A | 7 | a0001c0001t0001g0123 a0001c0001t0001g0151 a0001c0001t0002g0125 others(4): Show |
7 | HG00741.hp1 HG01109.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+49930G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184380 | |||||||
| chr2:85184445 | T | C | 13 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+49995T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184445 | |||||||
| chr2:85184461 | G | A | 12 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(9): Show |
12 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+50011G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184461 | |||||||
| chr2:85184675 | G | A | 12 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(9): Show |
12 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+50225G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184675 | |||||||
| chr2:85184759 | T | TGGTATAG others(58): Show |
1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.441+50313_441+5037 others(69): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85184759 | ||||||
| chr2:85184761 | G | A | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+50311G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85184761 | |||||||
| chr2:85185006 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.441+50556T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185006 | |||||||
| chr2:85185029 | G | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+50579G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185029 | |||||||
| chr2:85185196 | C | G | 1 | a0001c0001t0002g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.441+50746C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185196 | |||||||
| chr2:85185286 | G | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+50836G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185286 | |||||||
| chr2:85185298 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+50848C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185298 | |||||||
| chr2:85185528 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.441+51078G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185528 | |||||||
| chr2:85185622 | C | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+51172C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185622 | |||||||
| chr2:85185653 | T | C | 36 | a0001c0001t0001g0113 a0001c0001t0001g0139 a0001c0001t0001g0140 others(33): Show |
36 | HG01167.hp2 HG01243.hp1 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.441+51203T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185653 | |||||||
| chr2:85185711 | T | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+51261T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185711 | |||||||
| chr2:85185823 | G | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+51373G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185823 | |||||||
| chr2:85185945 | G | A | 103 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(100): Show |
103 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.441+51495G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185945 | |||||||
| chr2:85185958 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.441+51508G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185958 | |||||||
| chr2:85185959 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.441+51509G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85185959 | |||||||
| chr2:85185960 | A | AT | 47 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0088 others(44): Show |
47 | HG00597.hp1 HG01109.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.441+51534dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85185960 | ||||||
| chr2:85185960 | A | ATT | 29 | a0001c0001t0001g0141 a0001c0001t0001g0149 a0001c0001t0001g0161 others(26): Show |
29 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.441+51533_441+5153 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85185960 | ||||||
| chr2:85185960 | AT | A | 29 | a0001c0001t0001g0076 a0001c0001t0001g0090 a0001c0001t0001g0126 others(26): Show |
29 | HG00735.hp1 HG01106.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.441+51534delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85185960 | ||||||
| chr2:85186052 | T | C | 54 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(51): Show |
54 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.441+51602T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186052 | |||||||
| chr2:85186300 | A | G | 3 | a0001c0001t0002g0193 a0002c0002t0001g0037 a0002c0002t0003g0084 |
3 | HG02809.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.441+51850A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186300 | |||||||
| chr2:85186443 | C | CT | 51 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(48): Show |
51 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.441+51993_441+5199 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186443 | |||||||
| chr2:85186540 | T | C | 112 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(109): Show |
112 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.441+52090T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186540 | |||||||
| chr2:85186775 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+52325T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186775 | |||||||
| chr2:85186849 | T | C | 37 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(34): Show |
37 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.441+52399T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186849 | |||||||
| chr2:85186893 | A | C | 37 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(34): Show |
37 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.441+52443A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85186893 | |||||||
| chr2:85187017 | G | A | 154 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(151): Show |
154 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.441+52567G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187017 | |||||||
| chr2:85187197 | A | C | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+52747A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187197 | |||||||
| chr2:85187198 | G | C | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.441+52748G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187198 | |||||||
| chr2:85187214 | G | T | 1 | a0002c0002t0002g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.441+52764G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187214 | |||||||
| chr2:85187333 | A | C | 2 | a0001c0001t0001g0179 a0002c0002t0003g0078 |
2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.441+52883A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187333 | |||||||
| chr2:85187524 | G | A | 50 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(47): Show |
50 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.441+53074G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187524 | |||||||
| chr2:85187714 | C | G | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+53264C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187714 | |||||||
| chr2:85187730 | A | G | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+53280A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187730 | |||||||
| chr2:85187811 | T | C | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+53361T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187811 | |||||||
| chr2:85187843 | C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+53393C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187843 | |||||||
| chr2:85187894 | T | C | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+53444T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85187894 | |||||||
| chr2:85188115 | C | T | 1 | a0003c0004t0002g0106 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.441+53665C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188115 | |||||||
| chr2:85188306 | A | T | 148 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(145): Show |
148 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.441+53856A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188306 | |||||||
| chr2:85188312 | C | A | 8 | a0001c0001t0001g0092 a0001c0001t0001g0232 a0001c0001t0002g0067 others(5): Show |
8 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+53862C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188312 | |||||||
| chr2:85188345 | T | C | 2 | a0002c0002t0001g0009 a0002c0009t0001g0019 |
2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.441+53895T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188345 | |||||||
| chr2:85188350 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+53900G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188350 | |||||||
| chr2:85188369 | A | C | 3 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+53919A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188369 | |||||||
| chr2:85188423 | T | C | 2 | a0001c0001t0001g0179 a0002c0002t0003g0078 |
2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.441+53973T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188423 | |||||||
| chr2:85188680 | C | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+54230C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188680 | |||||||
| chr2:85188691 | G | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+54241G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188691 | |||||||
| chr2:85188815 | CT | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+54367delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85188815 | ||||||
| chr2:85188966 | T | A | 2 | a0002c0002t0001g0009 a0002c0009t0001g0019 |
2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.441+54516T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85188966 | |||||||
| chr2:85189170 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.441+54720T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189170 | |||||||
| chr2:85189173 | C | G | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0209 others(7): Show |
10 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+54723C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189173 | |||||||
| chr2:85189285 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.441+54835G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189285 | |||||||
| chr2:85189391 | A | G | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+54941A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189391 | |||||||
| chr2:85189579 | C | G | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+55129C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189579 | |||||||
| chr2:85189831 | A | G | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+55381A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189831 | |||||||
| chr2:85189990 | G | A | 1 | a0001c0001t0011g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.441+55540G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85189990 | |||||||
| chr2:85190119 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.441+55669C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85190119 | |||||||
| chr2:85190352 | C | T | 6 | a0001c0001t0001g0088 a0001c0001t0002g0157 a0001c0001t0002g0158 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+55902C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85190352 | |||||||
| chr2:85191586 | G | A | 1 | a0002c0002t0002g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.441+57136G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191586 | |||||||
| chr2:85191711 | G | C | 8 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(5): Show |
8 | HG02572.hp2 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+57261G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191711 | |||||||
| chr2:85191718 | G | C | 13 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+57268G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191718 | |||||||
| chr2:85191740 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.441+57290G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191740 | |||||||
| chr2:85191783 | T | C | 84 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(81): Show |
84 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.441+57333T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191783 | |||||||
| chr2:85191825 | C | CA | 20 | a0001c0001t0001g0090 a0001c0001t0001g0144 a0001c0001t0001g0161 others(17): Show |
20 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.441+57391dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85191825 | ||||||
| chr2:85191847 | T | C | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+57397T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191847 | |||||||
| chr2:85191901 | A | T | 1 | a0002c0002t0003g0176 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.441+57451A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85191901 | |||||||
| chr2:85192053 | T | C | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441+57603T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192053 | |||||||
| chr2:85192287 | CT | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+57838delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192287 | |||||||
| chr2:85192375 | G | T | 1 | a0001c0001t0002g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+57925G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192375 | |||||||
| chr2:85192398 | T | A | 27 | a0001c0001t0001g0090 a0001c0001t0001g0161 a0001c0001t0001g0163 others(24): Show |
27 | HG00735.hp1 HG02109.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.441+57948T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192398 | |||||||
| chr2:85192401 | T | A | 49 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(46): Show |
49 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+57951T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192401 | |||||||
| chr2:85192498 | A | G | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.441+58048A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192498 | |||||||
| chr2:85192524 | A | AT | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+58076dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192524 | ||||||
| chr2:85192641 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.441+58191C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192641 | |||||||
| chr2:85192661 | G | T | 31 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(28): Show |
31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+58211G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192661 | |||||||
| chr2:85192663 | G | T | 20 | a0001c0001t0001g0090 a0001c0001t0001g0234 a0001c0001t0002g0193 others(17): Show |
20 | HG00735.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.441+58213G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192663 | |||||||
| chr2:85192691 | C | CT | 23 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(20): Show |
23 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.441+58258dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192691 | ||||||
| chr2:85192691 | C | CTT | 8 | a0001c0001t0001g0209 a0001c0001t0002g0098 a0001c0001t0002g0206 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+58257_441+5825 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192691 | ||||||
| chr2:85192691 | CT | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0001g0234 others(7): Show |
10 | HG00735.hp1 HG01167.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+58258delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85192691 | ||||||
| chr2:85192777 | T | C | 217 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.441+58327T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85192777 | |||||||
| chr2:85193001 | C | T | 88 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(85): Show |
88 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.441+58551C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193001 | |||||||
| chr2:85193058 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+58608G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193058 | |||||||
| chr2:85193080 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.441+58630T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193080 | |||||||
| chr2:85193238 | G | A | 1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.441+58788G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193238 | |||||||
| chr2:85193359 | A | G | 138 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(135): Show |
138 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.441+58909A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193359 | |||||||
| chr2:85193399 | T | C | 2 | a0001c0001t0001g0179 a0002c0002t0003g0078 |
2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.441+58949T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193399 | |||||||
| chr2:85193407 | G | A | 49 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(46): Show |
49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+58957G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193407 | |||||||
| chr2:85193579 | T | C | 23 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(20): Show |
23 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.441+59129T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193579 | |||||||
| chr2:85193747 | T | C | 60 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(57): Show |
60 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.441+59297T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193747 | |||||||
| chr2:85193821 | G | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+59371G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193821 | |||||||
| chr2:85193894 | T | G | 19 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0170 others(16): Show |
19 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.441+59444T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193894 | |||||||
| chr2:85193968 | TA | T | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+59529delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85193968 | ||||||
| chr2:85193969 | A | T | 49 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(46): Show |
49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+59519A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85193969 | |||||||
| chr2:85194246 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.441+59796A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194246 | |||||||
| chr2:85194260 | G | C | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+59810G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194260 | |||||||
| chr2:85194300 | G | A | 13 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+59850G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194300 | |||||||
| chr2:85194398 | G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+59948G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194398 | |||||||
| chr2:85194568 | A | G | 49 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(46): Show |
49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+60118A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194568 | |||||||
| chr2:85194618 | C | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0211 |
2 | HG00597.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.441+60168C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194618 | |||||||
| chr2:85194657 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.441+60207G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194657 | |||||||
| chr2:85194670 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0005g0001 a0001c0001t0006g0003 |
3 | HG00741.hp2 HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.441+60220A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194670 | |||||||
| chr2:85194783 | G | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+60333G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194783 | |||||||
| chr2:85194784 | A | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+60334A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194784 | |||||||
| chr2:85194850 | C | T | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.441+60400C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85194850 | |||||||
| chr2:85195062 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.441+60612G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195062 | |||||||
| chr2:85195191 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.441+60741A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195191 | |||||||
| chr2:85195299 | C | T | 34 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(31): Show |
34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+60849C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195299 | |||||||
| chr2:85195413 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+60963G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195413 | |||||||
| chr2:85195494 | C | T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(5): Show |
8 | HG02572.hp2 HG02717.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+61044C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195494 | |||||||
| chr2:85195649 | A | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+61199A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195649 | |||||||
| chr2:85195695 | C | T | 84 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(81): Show |
84 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.441+61245C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195695 | |||||||
| chr2:85195860 | T | C | 49 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(46): Show |
49 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+61410T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195860 | |||||||
| chr2:85195870 | A | C | 34 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(31): Show |
34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+61420A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195870 | |||||||
| chr2:85195915 | T | A | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.441+61465T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85195915 | |||||||
| chr2:85196072 | T | C | 13 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+61622T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196072 | |||||||
| chr2:85196195 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.441+61745G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196195 | |||||||
| chr2:85196291 | C | T | 13 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0160 others(10): Show |
13 | HG01934.hp2 HG02056.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+61841C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196291 | |||||||
| chr2:85196454 | C | G | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+62004C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196454 | |||||||
| chr2:85196474 | G | A | 3 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0060 |
3 | HG00738.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.441+62024G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196474 | |||||||
| chr2:85196537 | A | AT | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02258.hp1 HG03041.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+62101dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85196537 | ||||||
| chr2:85196537 | AT | A | 13 | a0001c0001t0001g0076 a0001c0001t0001g0171 a0001c0001t0001g0234 others(10): Show |
13 | HG00735.hp1 HG01175.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+62101delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85196537 | ||||||
| chr2:85196657 | A | C | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.441+62207A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196657 | |||||||
| chr2:85196751 | A | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+62301A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196751 | |||||||
| chr2:85196895 | C | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(25): Show |
28 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.441+62445C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196895 | |||||||
| chr2:85196944 | C | T | 32 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(29): Show |
32 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+62494C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85196944 | |||||||
| chr2:85197001 | G | T | 1 | a0002c0002t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+62551G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197001 | |||||||
| chr2:85197007 | C | T | 13 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(10): Show |
13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+62557C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197007 | |||||||
| chr2:85197176 | C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+62726C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197176 | |||||||
| chr2:85197177 | G | A | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.441+62727G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197177 | |||||||
| chr2:85197437 | A | C | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.441+62987A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197437 | |||||||
| chr2:85197670 | T | C | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+63220T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197670 | |||||||
| chr2:85197702 | A | G | 28 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(25): Show |
28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+63252A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197702 | |||||||
| chr2:85197731 | C | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+63281C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197731 | |||||||
| chr2:85197784 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0002g0132 a0002c0002t0001g0093 others(1): Show |
4 | HG01243.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+63334C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197784 | |||||||
| chr2:85197864 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.441+63414A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197864 | |||||||
| chr2:85197925 | T | C | 59 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(56): Show |
59 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.441+63475T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85197925 | |||||||
| chr2:85198215 | C | G | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+63765C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198215 | |||||||
| chr2:85198237 | T | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+63787T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198237 | |||||||
| chr2:85198690 | G | A | 3 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.441+64240G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198690 | |||||||
| chr2:85198730 | A | T | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0002c0002t0002g0058 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+64280A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85198730 | |||||||
| chr2:85198985 | G | GT | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02572.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+64541dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85198985 | ||||||
| chr2:85199084 | CT | C | 2 | a0001c0001t0001g0199 a0001c0001t0002g0202 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.441+64635delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199084 | |||||||
| chr2:85199146 | T | C | 28 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(25): Show |
28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+64696T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199146 | |||||||
| chr2:85199286 | G | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+64836G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199286 | |||||||
| chr2:85199340 | A | G | 28 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(25): Show |
28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+64890A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199340 | |||||||
| chr2:85199601 | G | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+65151G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199601 | |||||||
| chr2:85199704 | C | T | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441+65254C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199704 | |||||||
| chr2:85199986 | G | A | 112 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(109): Show |
112 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.441+65536G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85199986 | |||||||
| chr2:85200127 | CA | C | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 others(1): Show |
4 | HG02258.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+65678delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200127 | |||||||
| chr2:85200580 | A | G | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+66130A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200580 | |||||||
| chr2:85200677 | G | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+66227G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200677 | |||||||
| chr2:85200818 | ATACCTGC others(11): Show |
A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0219 a0007c0013t0001g0143 |
3 | HG02129.hp1 HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.441+66406_441+6642 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85200818 | ||||||
| chr2:85200869 | G | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+66419G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85200869 | |||||||
| chr2:85201129 | G | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0219 a0007c0013t0001g0143 |
3 | HG02129.hp1 HG02135.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.441+66679G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201129 | |||||||
| chr2:85201197 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441+66747C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201197 | |||||||
| chr2:85201271 | A | G | 37 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(34): Show |
37 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.441+66821A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201271 | |||||||
| chr2:85201272 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.441+66822G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201272 | |||||||
| chr2:85201462 | T | G | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.441+67012T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201462 | |||||||
| chr2:85201604 | G | T | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+67154G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201604 | |||||||
| chr2:85201720 | G | A | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.441+67270G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201720 | |||||||
| chr2:85201737 | C | T | 48 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(45): Show |
48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.441+67287C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201737 | |||||||
| chr2:85201937 | TTTTA | T | 5 | a0001c0001t0001g0180 a0001c0001t0001g0209 a0002c0002t0002g0017 others(2): Show |
5 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+67515_441+6751 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85201937 | ||||||
| chr2:85201937 | TTTTATTT others(1): Show |
T | 132 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(129): Show |
132 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.441+67511_441+6751 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85201937 | ||||||
| chr2:85201950 | T | G | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+67500T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85201950 | |||||||
| chr2:85202025 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+67575C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202025 | |||||||
| chr2:85202075 | G | A | 31 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(28): Show |
31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+67625G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202075 | |||||||
| chr2:85202099 | A | G | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+67649A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202099 | |||||||
| chr2:85202316 | G | A | 1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441+67866G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202316 | |||||||
| chr2:85202377 | T | C | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+67927T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202377 | |||||||
| chr2:85202454 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+68004A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202454 | |||||||
| chr2:85202502 | T | C | 31 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(28): Show |
31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+68052T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202502 | |||||||
| chr2:85202690 | T | A | 1 | a0002c0002t0003g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.441+68240T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202690 | |||||||
| chr2:85202865 | G | A | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+68415G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202865 | |||||||
| chr2:85202902 | A | C | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.441+68452A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202902 | |||||||
| chr2:85202960 | A | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+68510A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202960 | |||||||
| chr2:85202979 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.441+68529A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85202979 | |||||||
| chr2:85203037 | A | G | 1 | a0002c0002t0001g0023 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.441+68587A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203037 | |||||||
| chr2:85203056 | T | C | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+68606T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203056 | |||||||
| chr2:85203081 | C | T | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+68631C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203081 | |||||||
| chr2:85203270 | A | G | 1 | a0006c0017t0001g0215 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.441+68820A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203270 | |||||||
| chr2:85203446 | A | G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0002c0002t0002g0017 others(3): Show |
6 | HG02572.hp1 HG03225.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+68996A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203446 | |||||||
| chr2:85203447 | T | C | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+68997T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203447 | |||||||
| chr2:85203465 | G | A | 34 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(31): Show |
34 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+69015G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203465 | |||||||
| chr2:85203511 | A | G | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69061A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203511 | |||||||
| chr2:85203572 | A | T | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69122A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203572 | |||||||
| chr2:85203576 | T | A | 24 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0170 others(21): Show |
24 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+69126T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203576 | |||||||
| chr2:85203746 | A | G | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69296A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203746 | |||||||
| chr2:85203862 | C | T | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69412C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203862 | |||||||
| chr2:85203889 | C | T | 13 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(10): Show |
13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+69439C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203889 | |||||||
| chr2:85203926 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.441+69476C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85203926 | |||||||
| chr2:85204291 | T | TC | 44 | a0001c0001t0001g0088 a0001c0001t0001g0112 a0001c0001t0001g0121 others(41): Show |
44 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.441+69855dupC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | ||||||
| chr2:85204291 | T | TCC | 68 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0095 others(65): Show |
68 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.441+69854_441+6985 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | ||||||
| chr2:85204291 | T | TCCC | 24 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(21): Show |
24 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+69853_441+6985 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | ||||||
| chr2:85204291 | TC | T | 18 | a0001c0001t0001g0138 a0001c0001t0001g0212 a0001c0001t0001g0229 others(15): Show |
18 | HG00735.hp1 HG00741.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.441+69855delC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204291 | ||||||
| chr2:85204296 | C | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+69846C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204296 | |||||||
| chr2:85204334 | G | C | 2 | a0001c0001t0002g0125 a0002c0002t0001g0109 |
2 | NA18959.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.441+69884G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204334 | |||||||
| chr2:85204420 | G | A | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+69970G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204420 | |||||||
| chr2:85204618 | CA | C | 31 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(28): Show |
31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+70171delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204618 | ||||||
| chr2:85204831 | AT | A | 14 | a0001c0001t0001g0124 a0001c0001t0001g0161 a0001c0001t0001g0163 others(11): Show |
14 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+70392delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204831 | ||||||
| chr2:85204844 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.441+70394A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204844 | |||||||
| chr2:85204883 | T | G | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+70433T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204883 | |||||||
| chr2:85204884 | TG | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(7): Show |
10 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+70435delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204884 | |||||||
| chr2:85204885 | G | GT | 104 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(101): Show |
104 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.441+70438dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85204885 | ||||||
| chr2:85204885 | G | T | 1 | a0001c0001t0002g0167 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.441+70435G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204885 | |||||||
| chr2:85204889 | G | T | 132 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(129): Show |
132 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.441+70439G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204889 | |||||||
| chr2:85204931 | C | G | 1 | a0002c0002t0002g0027 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.441+70481C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85204931 | |||||||
| chr2:85205281 | A | C | 28 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(25): Show |
28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+70831A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205281 | |||||||
| chr2:85205337 | T | C | 28 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(25): Show |
28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+70887T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205337 | |||||||
| chr2:85205466 | G | C | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+71016G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205466 | |||||||
| chr2:85205535 | T | TTC | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+71086_441+7108 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85205535 | ||||||
| chr2:85205536 | TG | T | 107 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(104): Show |
107 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.441+71087delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205536 | |||||||
| chr2:85205537 | G | C | 16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0209 others(13): Show |
16 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+71087G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205537 | |||||||
| chr2:85205537 | G | T | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+71087G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205537 | |||||||
| chr2:85205538 | T | C | 107 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(104): Show |
107 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.441+71088T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205538 | |||||||
| chr2:85205539 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.441+71089T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205539 | |||||||
| chr2:85205580 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.441+71130G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205580 | |||||||
| chr2:85205702 | G | A | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.441+71252G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205702 | |||||||
| chr2:85205737 | T | C | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+71287T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205737 | |||||||
| chr2:85205818 | G | C | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+71368G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205818 | |||||||
| chr2:85205827 | T | C | 30 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(27): Show |
30 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+71377T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205827 | |||||||
| chr2:85205969 | A | G | 2 | a0001c0001t0001g0136 a0002c0002t0001g0034 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.441+71519A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85205969 | |||||||
| chr2:85206064 | T | C | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+71614T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206064 | |||||||
| chr2:85206147 | G | A | 31 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(28): Show |
31 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+71697G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206147 | |||||||
| chr2:85206279 | G | A | 28 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(25): Show |
28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+71829G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206279 | |||||||
| chr2:85206300 | C | T | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+71850C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206300 | |||||||
| chr2:85206343 | T | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+71893T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206343 | |||||||
| chr2:85206471 | T | C | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.441+72021T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206471 | |||||||
| chr2:85206670 | G | T | 24 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0170 others(21): Show |
24 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.441+72220G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206670 | |||||||
| chr2:85206724 | T | C | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+72274T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206724 | |||||||
| chr2:85206833 | A | G | 10 | a0001c0001t0001g0149 a0001c0001t0001g0199 a0001c0001t0001g0201 others(7): Show |
10 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+72383A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206833 | |||||||
| chr2:85206966 | AAC | A | 48 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(45): Show |
48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.441+72518_441+7251 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85206966 | ||||||
| chr2:85206981 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+72531C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206981 | |||||||
| chr2:85206985 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.441+72535C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85206985 | |||||||
| chr2:85207250 | A | G | 1 | a0002c0002t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.441+72800A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207250 | |||||||
| chr2:85207309 | A | C | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.441+72859A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207309 | |||||||
| chr2:85207372 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.441+72922C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207372 | |||||||
| chr2:85207417 | C | T | 211 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0076 others(208): Show |
211 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.441+72967C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207417 | |||||||
| chr2:85207446 | T | C | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+72996T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207446 | |||||||
| chr2:85207489 | A | G | 48 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(45): Show |
48 | HG00280.hp2 HG00597.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.441+73039A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207489 | |||||||
| chr2:85207654 | G | A | 25 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0170 others(22): Show |
25 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.441+73204G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207654 | |||||||
| chr2:85207699 | T | G | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+73249T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207699 | |||||||
| chr2:85207706 | A | G | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.441+73256A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207706 | |||||||
| chr2:85207807 | C | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.441+73357C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207807 | |||||||
| chr2:85207916 | T | G | 30 | a0001c0001t0001g0031 a0001c0001t0001g0139 a0001c0001t0001g0140 others(27): Show |
30 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.441+73466T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207916 | |||||||
| chr2:85207997 | C | T | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(10): Show |
13 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+73547C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207997 | |||||||
| chr2:85207999 | C | T | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+73549C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85207999 | |||||||
| chr2:85208031 | T | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+73581T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208031 | |||||||
| chr2:85208101 | T | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+73651T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208101 | |||||||
| chr2:85208158 | G | A | 12 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(9): Show |
12 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+73708G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208158 | |||||||
| chr2:85208239 | G | A | 14 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(11): Show |
14 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+73789G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208239 | |||||||
| chr2:85208346 | A | G | 14 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(11): Show |
14 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+73896A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208346 | |||||||
| chr2:85208574 | A | G | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+74124A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208574 | |||||||
| chr2:85208611 | T | C | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.441+74161T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208611 | |||||||
| chr2:85208821 | A | G | 139 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(136): Show |
139 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.441+74371A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208821 | |||||||
| chr2:85208827 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+74377A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208827 | |||||||
| chr2:85208998 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.442-74497G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85208998 | |||||||
| chr2:85209052 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.442-74443G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209052 | |||||||
| chr2:85209162 | GT | G | 126 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(123): Show |
126 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.442-74331delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85209162 | ||||||
| chr2:85209423 | G | A | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-74072G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209423 | |||||||
| chr2:85209583 | G | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-73912G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209583 | |||||||
| chr2:85209691 | C | A | 2 | a0002c0003t0002g0086 a0004c0012t0002g0184 |
2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.442-73804C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209691 | |||||||
| chr2:85209761 | C | T | 30 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(27): Show |
30 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.442-73734C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85209761 | |||||||
| chr2:85210297 | G | T | 115 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(112): Show |
115 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.442-73198G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210297 | |||||||
| chr2:85210314 | A | G | 115 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(112): Show |
115 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.442-73181A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210314 | |||||||
| chr2:85210361 | G | A | 28 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(25): Show |
28 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-73134G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210361 | |||||||
| chr2:85210443 | C | T | 1 | a0002c0002t0002g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.442-73052C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210443 | |||||||
| chr2:85210614 | G | A | 3 | a0001c0001t0002g0193 a0002c0002t0001g0037 a0002c0002t0003g0084 |
3 | HG02809.hp2 HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.442-72881G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210614 | |||||||
| chr2:85210694 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-72801G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210694 | |||||||
| chr2:85210822 | C | T | 109 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(106): Show |
109 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.442-72673C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210822 | |||||||
| chr2:85210877 | G | A | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-72618G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210877 | |||||||
| chr2:85210942 | C | T | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-72553C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210942 | |||||||
| chr2:85210944 | C | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-72551C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85210944 | |||||||
| chr2:85211153 | A | G | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-72342A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85211153 | |||||||
| chr2:85211224 | TA | T | 86 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(83): Show |
86 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.442-72269delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85211224 | ||||||
| chr2:85211417 | C | T | 30 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0101 others(27): Show |
30 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.442-72078C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85211417 | |||||||
| chr2:85211786 | G | T | 122 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(119): Show |
122 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.442-71709G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85211786 | |||||||
| chr2:85212046 | C | T | 33 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(30): Show |
33 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-71449C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212046 | |||||||
| chr2:85212089 | C | CA | 19 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0191 others(16): Show |
19 | HG00621.hp1 HG00735.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-71379dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | ||||||
| chr2:85212089 | C | CAA | 17 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0104 others(14): Show |
17 | HG00597.hp1 HG01071.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-71380_442-7137 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | ||||||
| chr2:85212089 | CA | C | 75 | a0001c0001t0001g0014 a0001c0001t0001g0097 a0001c0001t0001g0111 others(72): Show |
75 | HG00280.hp1 HG00621.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.442-71379delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | ||||||
| chr2:85212089 | CAA | C | 57 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0096 others(54): Show |
57 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.442-71380_442-7137 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | ||||||
| chr2:85212089 | CAAA | C | 8 | a0001c0001t0002g0165 a0001c0001t0002g0206 a0001c0001t0002g0207 others(5): Show |
8 | HG01167.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-71381_442-7137 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | ||||||
| chr2:85212089 | CAAAAAAA others(1): Show |
C | 27 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0145 others(24): Show |
27 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-71386_442-7137 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | ||||||
| chr2:85212089 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-71392_442-7137 others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85212089 | ||||||
| chr2:85212220 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0002g0102 a0002c0002t0001g0022 others(1): Show |
4 | HG01071.hp1 HG01346.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-71275C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212220 | |||||||
| chr2:85212430 | T | C | 135 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(132): Show |
135 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.442-71065T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212430 | |||||||
| chr2:85212650 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.442-70845G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212650 | |||||||
| chr2:85212748 | A | G | 37 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0095 others(34): Show |
37 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-70747A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212748 | |||||||
| chr2:85212828 | C | A | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-70667C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212828 | |||||||
| chr2:85212867 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-70628A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85212867 | |||||||
| chr2:85213026 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442-70469G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213026 | |||||||
| chr2:85213043 | G | A | 3 | a0001c0001t0001g0209 a0002c0003t0002g0086 a0004c0012t0002g0184 |
3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.442-70452G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213043 | |||||||
| chr2:85213275 | A | G | 140 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(137): Show |
140 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.442-70220A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213275 | |||||||
| chr2:85213300 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-70195A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213300 | |||||||
| chr2:85213713 | T | C | 15 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(12): Show |
15 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-69782T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85213713 | |||||||
| chr2:85214106 | G | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-69389G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214106 | |||||||
| chr2:85214112 | C | A | 2 | a0002c0002t0001g0042 a0002c0002t0002g0044 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.442-69383C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214112 | |||||||
| chr2:85214137 | G | T | 1 | a0002c0002t0002g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.442-69358G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214137 | |||||||
| chr2:85214248 | T | C | 1 | a0002c0002t0001g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.442-69247T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214248 | |||||||
| chr2:85214276 | A | G | 46 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0111 others(43): Show |
46 | HG00280.hp1 HG00621.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-69219A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214276 | |||||||
| chr2:85214689 | A | G | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-68806A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214689 | |||||||
| chr2:85214728 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-68767G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214728 | |||||||
| chr2:85214748 | A | G | 12 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(9): Show |
12 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-68747A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214748 | |||||||
| chr2:85214815 | T | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-68680T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214815 | |||||||
| chr2:85214945 | T | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-68550T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214945 | |||||||
| chr2:85214958 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.442-68537A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85214958 | |||||||
| chr2:85215057 | C | T | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(8): Show |
11 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-68438C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215057 | |||||||
| chr2:85215161 | C | T | 4 | a0001c0001t0001g0197 a0001c0001t0002g0185 a0001c0001t0002g0196 others(1): Show |
4 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-68334C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215161 | |||||||
| chr2:85215167 | C | G | 28 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0131 others(25): Show |
28 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-68328C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215167 | |||||||
| chr2:85215213 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.442-68282T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215213 | |||||||
| chr2:85215227 | G | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.442-68268G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215227 | |||||||
| chr2:85215365 | A | G | 28 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0131 others(25): Show |
28 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-68130A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215365 | |||||||
| chr2:85215617 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0167 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-67878G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215617 | |||||||
| chr2:85215767 | T | TG | 20 | a0001c0001t0001g0031 a0001c0001t0001g0112 a0001c0001t0001g0122 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.442-67719dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85215767 | ||||||
| chr2:85215767 | TG | T | 16 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(13): Show |
16 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-67719delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85215767 | ||||||
| chr2:85215916 | C | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-67579C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85215916 | |||||||
| chr2:85216047 | G | C | 21 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0170 others(18): Show |
21 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-67448G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216047 | |||||||
| chr2:85216246 | G | A | 40 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0001g0124 others(37): Show |
40 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.442-67249G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216246 | |||||||
| chr2:85216256 | G | A | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-67239G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216256 | |||||||
| chr2:85216420 | G | A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01256.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-67075G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216420 | |||||||
| chr2:85216527 | G | A | 153 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(150): Show |
153 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(150): Show |
intron_variant | MODIFIER | c.442-66968G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216527 | |||||||
| chr2:85216583 | T | C | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-66912T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216583 | |||||||
| chr2:85216625 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-66870G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216625 | |||||||
| chr2:85216669 | G | T | 2 | a0002c0003t0002g0086 a0004c0012t0002g0184 |
2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.442-66826G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216669 | |||||||
| chr2:85216697 | G | A | 26 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0131 others(23): Show |
26 | HG00597.hp2 HG00639.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.442-66798G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216697 | |||||||
| chr2:85216711 | G | T | 2 | a0002c0003t0002g0086 a0004c0012t0002g0184 |
2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.442-66784G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216711 | |||||||
| chr2:85216801 | G | A | 94 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0096 others(91): Show |
94 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.442-66694G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216801 | |||||||
| chr2:85216962 | C | A | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-66533C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85216962 | |||||||
| chr2:85217252 | C | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-66243C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217252 | |||||||
| chr2:85217456 | C | T | 21 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0104 others(18): Show |
21 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-66039C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217456 | |||||||
| chr2:85217604 | C | G | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(6): Show |
9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-65891C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217604 | |||||||
| chr2:85217781 | A | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-65714A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85217781 | |||||||
| chr2:85218236 | T | TTTTA | 47 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(44): Show |
47 | HG01106.hp2 HG01175.hp2 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.442-65227_442-6522 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | ||||||
| chr2:85218236 | T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0197 a0002c0002t0001g0057 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-65231_442-6522 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | ||||||
| chr2:85218236 | T | TTTTATTT others(5): Show |
1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.442-65235_442-6522 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | ||||||
| chr2:85218236 | T | TTTTATTT others(9): Show |
8 | a0001c0001t0001g0234 a0001c0001t0002g0206 a0001c0001t0002g0207 others(5): Show |
8 | HG00735.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-65239_442-6522 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218236 | ||||||
| chr2:85218403 | A | T | 13 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(10): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-65092A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218403 | |||||||
| chr2:85218548 | G | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64947G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218548 | |||||||
| chr2:85218638 | A | AG | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64857_442-6485 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218638 | |||||||
| chr2:85218639 | T | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64856T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218639 | |||||||
| chr2:85218639 | T | TGG | 16 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0001g0126 others(13): Show |
16 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-64848_442-6484 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85218639 | ||||||
| chr2:85218648 | G | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 others(1): Show |
4 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-64847G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218648 | |||||||
| chr2:85218649 | A | G | 41 | a0001c0001t0001g0090 a0001c0001t0001g0136 a0001c0001t0001g0145 others(38): Show |
41 | HG00280.hp2 HG00735.hp1 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.442-64846A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218649 | |||||||
| chr2:85218650 | A | G | 6 | a0001c0001t0001g0031 a0001c0001t0002g0206 a0001c0001t0002g0207 others(3): Show |
6 | HG02258.hp1 HG02818.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-64845A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218650 | |||||||
| chr2:85218762 | T | C | 4 | a0001c0001t0001g0197 a0001c0001t0002g0185 a0001c0001t0002g0196 others(1): Show |
4 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-64733T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218762 | |||||||
| chr2:85218993 | G | A | 2 | a0001c0001t0001g0179 a0002c0002t0003g0078 |
2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.442-64502G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85218993 | |||||||
| chr2:85219043 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-64452C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219043 | |||||||
| chr2:85219066 | T | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-64429T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219066 | |||||||
| chr2:85219161 | A | AT | 13 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(10): Show |
13 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-64326dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85219161 | ||||||
| chr2:85219169 | T | C | 19 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0145 others(16): Show |
19 | HG01934.hp2 HG02056.hp2 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-64326T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219169 | |||||||
| chr2:85219321 | A | G | 32 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(29): Show |
32 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.442-64174A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219321 | |||||||
| chr2:85219363 | A | G | 94 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0096 others(91): Show |
94 | HG00597.hp2 HG00639.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.442-64132A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219363 | |||||||
| chr2:85219398 | A | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-64097A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219398 | |||||||
| chr2:85219402 | CA | C | 2 | a0002c0002t0001g0069 a0002c0002t0001g0081 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-64091delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85219402 | ||||||
| chr2:85219560 | C | G | 1 | a0002c0002t0001g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.442-63935C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219560 | |||||||
| chr2:85219876 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442-63619G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219876 | |||||||
| chr2:85219901 | T | A | 32 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(29): Show |
32 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.442-63594T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219901 | |||||||
| chr2:85219940 | A | G | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-63555A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85219940 | |||||||
| chr2:85220217 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-63278A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220217 | |||||||
| chr2:85220320 | T | G | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(6): Show |
9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-63175T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220320 | |||||||
| chr2:85220359 | A | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-63136A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220359 | |||||||
| chr2:85220361 | A | T | 159 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(156): Show |
159 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.442-63134A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220361 | |||||||
| chr2:85220393 | T | C | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(6): Show |
9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-63102T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220393 | |||||||
| chr2:85220412 | A | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-63083A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220412 | |||||||
| chr2:85220449 | A | ACCT | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(6): Show |
9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-63040_442-6303 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85220449 | ||||||
| chr2:85220586 | G | A | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(5): Show |
8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-62909G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220586 | |||||||
| chr2:85220600 | G | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-62895G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220600 | |||||||
| chr2:85220707 | C | T | 132 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(129): Show |
132 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.442-62788C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220707 | |||||||
| chr2:85220807 | G | C | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-62688G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220807 | |||||||
| chr2:85220896 | A | G | 1 | a0005c0006t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.442-62599A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85220896 | |||||||
| chr2:85221102 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-62393C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221102 | |||||||
| chr2:85221233 | G | A | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(6): Show |
9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-62262G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221233 | |||||||
| chr2:85221368 | A | G | 4 | a0001c0001t0001g0197 a0001c0001t0002g0185 a0001c0001t0002g0196 others(1): Show |
4 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-62127A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221368 | |||||||
| chr2:85221372 | G | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-62123G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221372 | |||||||
| chr2:85221507 | G | C | 4 | a0001c0001t0001g0088 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-61988G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221507 | |||||||
| chr2:85221546 | A | G | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-61949A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221546 | |||||||
| chr2:85221557 | G | A | 2 | a0002c0002t0001g0037 a0002c0002t0003g0084 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.442-61938G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221557 | |||||||
| chr2:85221732 | C | G | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(6): Show |
9 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-61763C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221732 | |||||||
| chr2:85221899 | A | G | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-61596A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221899 | |||||||
| chr2:85221913 | A | C | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-61582A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221913 | |||||||
| chr2:85221931 | T | TA | 85 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0096 others(82): Show |
85 | HG00597.hp2 HG00735.hp1 HG01071.hp2 others(82): Show |
intron_variant | MODIFIER | c.442-61550dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85221931 | ||||||
| chr2:85221956 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-61539A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221956 | |||||||
| chr2:85221992 | G | A | 1 | a0002c0002t0002g0039 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.442-61503G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85221992 | |||||||
| chr2:85222069 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.442-61426C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222069 | |||||||
| chr2:85222108 | G | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-61387G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222108 | |||||||
| chr2:85222197 | C | T | 17 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0131 others(14): Show |
17 | HG00597.hp2 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-61298C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222197 | |||||||
| chr2:85222201 | C | T | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-61294C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222201 | |||||||
| chr2:85222256 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-61239G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222256 | |||||||
| chr2:85222311 | G | C | 1 | a0002c0002t0012g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.442-61184G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222311 | |||||||
| chr2:85222348 | A | AC | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-61147_442-6114 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222348 | |||||||
| chr2:85222348 | A | C | 13 | a0001c0001t0001g0148 a0001c0001t0001g0161 a0001c0001t0001g0163 others(10): Show |
13 | HG00639.hp2 HG02145.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-61147A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222348 | |||||||
| chr2:85222351 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.442-61144A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222351 | |||||||
| chr2:85222352 | C | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-61143C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222352 | |||||||
| chr2:85222361 | AAAC | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0099 others(15): Show |
18 | HG00280.hp2 HG01106.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-61131_442-6112 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222361 | ||||||
| chr2:85222364 | C | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0226 a0002c0002t0002g0017 |
3 | HG02056.hp1 HG06807.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.442-61131C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222364 | |||||||
| chr2:85222368 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.442-61127A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222368 | |||||||
| chr2:85222375 | A | C | 32 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(29): Show |
32 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.442-61120A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222375 | |||||||
| chr2:85222417 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.442-61078C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222417 | |||||||
| chr2:85222485 | T | C | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-61010T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222485 | |||||||
| chr2:85222534 | G | A | 1 | a0002c0002t0001g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-60961G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222534 | |||||||
| chr2:85222600 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.442-60895G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222600 | |||||||
| chr2:85222618 | C | G | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-60877C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222618 | |||||||
| chr2:85222669 | C | CA | 25 | a0001c0001t0001g0076 a0001c0001t0001g0113 a0001c0001t0001g0138 others(22): Show |
25 | HG00735.hp2 HG02129.hp1 HG02129.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-60806dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | ||||||
| chr2:85222669 | C | CAA | 54 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0096 others(51): Show |
54 | HG00597.hp2 HG01243.hp1 HG01934.hp2 others(51): Show |
intron_variant | MODIFIER | c.442-60807_442-6080 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | ||||||
| chr2:85222669 | C | CAAA | 14 | a0001c0001t0001g0149 a0001c0001t0001g0156 a0001c0001t0001g0199 others(11): Show |
14 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-60808_442-6080 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | ||||||
| chr2:85222669 | C | CAAAA | 14 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0190 others(11): Show |
14 | HG01071.hp2 HG01109.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-60809_442-6080 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | ||||||
| chr2:85222669 | C | CAAAAA | 7 | a0001c0001t0001g0234 a0002c0002t0001g0040 a0002c0002t0001g0062 others(4): Show |
7 | HG00735.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-60810_442-6080 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85222669 | ||||||
| chr2:85222685 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.442-60810A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222685 | |||||||
| chr2:85222909 | G | A | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-60586G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85222909 | |||||||
| chr2:85223212 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.442-60283G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223212 | |||||||
| chr2:85223238 | C | T | 16 | a0001c0001t0001g0096 a0001c0001t0001g0124 a0001c0001t0001g0131 others(13): Show |
16 | HG00597.hp2 HG01071.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-60257C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223238 | |||||||
| chr2:85223486 | G | A | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-60009G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223486 | |||||||
| chr2:85223582 | T | TG | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.442-59911dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85223582 | ||||||
| chr2:85223691 | G | A | 13 | a0001c0001t0001g0031 a0001c0001t0001g0199 a0001c0001t0001g0201 others(10): Show |
13 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-59804G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223691 | |||||||
| chr2:85223813 | A | G | 4 | a0001c0001t0001g0209 a0002c0002t0002g0017 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-59682A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223813 | |||||||
| chr2:85223836 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0002g0202 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.442-59659C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85223836 | |||||||
| chr2:85224018 | A | T | 6 | a0001c0001t0001g0232 a0001c0001t0002g0067 a0002c0002t0001g0009 others(3): Show |
6 | HG02451.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-59477A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224018 | |||||||
| chr2:85224123 | G | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(5): Show |
8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-59372G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224123 | |||||||
| chr2:85224238 | A | G | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(5): Show |
8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-59257A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224238 | |||||||
| chr2:85224424 | A | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(5): Show |
8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-59071A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224424 | |||||||
| chr2:85224540 | A | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-58955A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224540 | |||||||
| chr2:85224760 | T | C | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-58735T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224760 | |||||||
| chr2:85224997 | T | C | 3 | a0001c0001t0002g0116 a0002c0002t0001g0056 a0002c0002t0002g0047 |
3 | NA18951.hp2 NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.442-58498T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85224997 | |||||||
| chr2:85225623 | A | AT | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0002c0002t0002g0058 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-57868dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85225623 | ||||||
| chr2:85225854 | C | T | 1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.442-57641C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85225854 | |||||||
| chr2:85225855 | G | A | 2 | a0002c0002t0001g0089 a0002c0002t0002g0043 |
2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.442-57640G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85225855 | |||||||
| chr2:85225988 | T | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(5): Show |
8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-57507T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85225988 | |||||||
| chr2:85226448 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-57047A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226448 | |||||||
| chr2:85226470 | T | C | 90 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0096 others(87): Show |
90 | HG00597.hp2 HG00735.hp1 HG01071.hp2 others(87): Show |
intron_variant | MODIFIER | c.442-57025T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226470 | |||||||
| chr2:85226544 | G | GT | 12 | a0001c0001t0001g0031 a0001c0001t0001g0199 a0001c0001t0001g0201 others(9): Show |
12 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-56947dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226544 | ||||||
| chr2:85226590 | T | TCTC | 156 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0076 others(153): Show |
156 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.442-56905_442-5690 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226590 | |||||||
| chr2:85226737 | A | G | 33 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(30): Show |
33 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-56758A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226737 | |||||||
| chr2:85226816 | CT | C | 46 | a0001c0001t0001g0031 a0001c0001t0001g0096 a0001c0001t0001g0108 others(43): Show |
46 | HG00597.hp2 HG01071.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-56661delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226816 | ||||||
| chr2:85226816 | CTT | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0229 a0001c0001t0002g0206 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-56662_442-5666 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226816 | ||||||
| chr2:85226816 | CTTT | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0234 others(5): Show |
8 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-56663_442-5666 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85226816 | ||||||
| chr2:85226916 | A | T | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56579A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226916 | |||||||
| chr2:85226972 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-56523C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85226972 | |||||||
| chr2:85227134 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-56361G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227134 | |||||||
| chr2:85227165 | A | G | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56330A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227165 | |||||||
| chr2:85227246 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0005g0001 a0001c0001t0006g0003 |
3 | HG00741.hp2 HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.442-56249T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227246 | |||||||
| chr2:85227302 | T | C | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56193T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227302 | |||||||
| chr2:85227438 | C | CTT | 5 | a0001c0001t0001g0234 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-56044_442-5604 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227438 | ||||||
| chr2:85227438 | CT | C | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01256.hp1 HG01517.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-56043delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227438 | ||||||
| chr2:85227456 | CAAGTAAG others(6): Show |
C | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.442-56035_442-5602 others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227456 | ||||||
| chr2:85227551 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55944C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227551 | |||||||
| chr2:85227685 | C | G | 14 | a0001c0001t0001g0031 a0001c0001t0001g0149 a0001c0001t0001g0199 others(11): Show |
14 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-55810C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227685 | |||||||
| chr2:85227738 | A | G | 18 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0170 others(15): Show |
18 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-55757A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227738 | |||||||
| chr2:85227764 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0002g0165 |
2 | HG01167.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.442-55731G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227764 | |||||||
| chr2:85227861 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55634G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227861 | |||||||
| chr2:85227925 | A | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0182 a0001c0001t0002g0165 |
3 | HG01167.hp1 HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.442-55570A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85227925 | |||||||
| chr2:85227992 | C | CA | 71 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0112 others(68): Show |
71 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.442-55479dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227992 | ||||||
| chr2:85227992 | C | CAA | 13 | a0001c0001t0001g0120 a0001c0001t0001g0123 a0001c0001t0001g0133 others(10): Show |
13 | HG00621.hp2 HG01175.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.442-55480_442-5547 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227992 | ||||||
| chr2:85227992 | CA | C | 24 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(21): Show |
24 | HG00735.hp1 HG01175.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.442-55479delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85227992 | ||||||
| chr2:85228017 | T | A | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-55478T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228017 | |||||||
| chr2:85228035 | A | G | 13 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(10): Show |
13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-55460A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228035 | |||||||
| chr2:85228048 | A | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55447A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228048 | |||||||
| chr2:85228067 | A | T | 1 | a0010c0011t0002g0231 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442-55428A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228067 | |||||||
| chr2:85228240 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.442-55255C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228240 | |||||||
| chr2:85228254 | T | C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-55241T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228254 | |||||||
| chr2:85228336 | C | T | 1 | a0002c0007t0002g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-55159C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228336 | |||||||
| chr2:85228552 | C | T | 34 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(31): Show |
34 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.442-54943C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228552 | |||||||
| chr2:85228763 | C | T | 3 | a0001c0001t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG02818.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.442-54732C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228763 | |||||||
| chr2:85228816 | C | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-54679C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228816 | |||||||
| chr2:85228831 | C | T | 2 | a0002c0002t0001g0069 a0002c0002t0001g0081 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-54664C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228831 | |||||||
| chr2:85228843 | A | G | 87 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(84): Show |
87 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.442-54652A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228843 | |||||||
| chr2:85228978 | G | A | 1 | a0002c0002t0002g0065 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.442-54517G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85228978 | |||||||
| chr2:85229015 | T | C | 218 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0076 others(215): Show |
218 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(215): Show |
intron_variant | MODIFIER | c.442-54480T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229015 | |||||||
| chr2:85229020 | C | CA | 37 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0131 others(34): Show |
37 | HG00597.hp2 HG00735.hp1 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-54456dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85229020 | ||||||
| chr2:85229020 | C | CAA | 21 | a0001c0001t0001g0031 a0001c0001t0001g0199 a0001c0001t0001g0201 others(18): Show |
21 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.442-54457_442-5445 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85229020 | ||||||
| chr2:85229020 | CA | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0107 a0002c0002t0001g0025 others(2): Show |
5 | HG01975.hp1 HG02647.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-54456delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85229020 | ||||||
| chr2:85229036 | A | G | 1 | a0001c0001t0011g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.442-54459A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229036 | |||||||
| chr2:85229078 | G | A | 2 | a0002c0002t0001g0062 a0002c0002t0002g0061 |
2 | HG00735.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-54417G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229078 | |||||||
| chr2:85229085 | G | A | 12 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0002c0002t0001g0007 others(9): Show |
12 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-54410G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229085 | |||||||
| chr2:85229117 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.442-54378C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229117 | |||||||
| chr2:85229118 | G | A | 9 | a0001c0001t0001g0232 a0001c0001t0002g0067 a0001c0001t0002g0167 others(6): Show |
9 | HG02451.hp2 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-54377G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229118 | |||||||
| chr2:85229198 | T | C | 33 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(30): Show |
33 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-54297T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229198 | |||||||
| chr2:85229299 | A | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-54196A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229299 | |||||||
| chr2:85229426 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.442-54069C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229426 | |||||||
| chr2:85229654 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0124 |
2 | NA18953.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.442-53841G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229654 | |||||||
| chr2:85229762 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-53733C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229762 | |||||||
| chr2:85229825 | T | C | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-53670T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85229825 | |||||||
| chr2:85230332 | G | T | 2 | a0001c0001t0005g0001 a0001c0001t0006g0003 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.442-53163G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230332 | |||||||
| chr2:85230615 | A | G | 22 | a0001c0001t0001g0156 a0001c0001t0001g0170 a0001c0001t0001g0171 others(19): Show |
22 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.442-52880A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230615 | |||||||
| chr2:85230829 | A | G | 33 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(30): Show |
33 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-52666A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230829 | |||||||
| chr2:85230931 | A | G | 28 | a0001c0001t0001g0156 a0001c0001t0001g0170 a0001c0001t0001g0171 others(25): Show |
28 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-52564A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85230931 | |||||||
| chr2:85231088 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.442-52407C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231088 | |||||||
| chr2:85231100 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-52395C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231100 | |||||||
| chr2:85231140 | T | C | 3 | a0001c0001t0002g0129 a0002c0002t0001g0064 a0002c0002t0002g0063 |
3 | HG01074.hp2 HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.442-52355T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231140 | |||||||
| chr2:85231247 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.442-52248C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231247 | |||||||
| chr2:85231255 | C | T | 13 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(10): Show |
13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-52240C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231255 | |||||||
| chr2:85231534 | T | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-51961T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231534 | |||||||
| chr2:85231654 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.442-51841C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231654 | |||||||
| chr2:85231655 | G | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-51840G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231655 | |||||||
| chr2:85231777 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.442-51718C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231777 | |||||||
| chr2:85231778 | G | A | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-51717G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231778 | |||||||
| chr2:85231913 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-51582C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85231913 | |||||||
| chr2:85231972 | GGATTGAG others(11): Show |
G | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-51520_442-5150 others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85231972 | ||||||
| chr2:85232071 | A | G | 22 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(19): Show |
22 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-51424A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232071 | |||||||
| chr2:85232283 | G | A | 1 | a0001c0001t0005g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.442-51212G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232283 | |||||||
| chr2:85232504 | G | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-50991G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232504 | |||||||
| chr2:85232559 | G | T | 33 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(30): Show |
33 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-50936G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232559 | |||||||
| chr2:85232757 | A | G | 80 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(77): Show |
80 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(77): Show |
intron_variant | MODIFIER | c.442-50738A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232757 | |||||||
| chr2:85232992 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-50503C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85232992 | |||||||
| chr2:85233316 | AT | A | 141 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0088 others(138): Show |
141 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.442-50160delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85233316 | ||||||
| chr2:85233316 | ATT | A | 30 | a0001c0001t0001g0031 a0001c0001t0001g0156 a0001c0001t0001g0161 others(27): Show |
30 | HG01167.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.442-50161_442-5016 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85233316 | ||||||
| chr2:85233316 | ATTT | A | 41 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(38): Show |
41 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.442-50162_442-5016 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85233316 | ||||||
| chr2:85233382 | T | C | 215 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0076 others(212): Show |
215 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(212): Show |
intron_variant | MODIFIER | c.442-50113T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233382 | |||||||
| chr2:85233387 | T | C | 83 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(80): Show |
83 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(80): Show |
intron_variant | MODIFIER | c.442-50108T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233387 | |||||||
| chr2:85233472 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.442-50023C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233472 | |||||||
| chr2:85233556 | T | C | 84 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(81): Show |
84 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(81): Show |
intron_variant | MODIFIER | c.442-49939T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233556 | |||||||
| chr2:85233561 | G | A | 2 | a0001c0001t0001g0223 a0002c0002t0002g0020 |
2 | HG01346.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.442-49934G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233561 | |||||||
| chr2:85233813 | G | A | 39 | a0001c0001t0001g0031 a0001c0001t0001g0156 a0001c0001t0001g0161 others(36): Show |
39 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.442-49682G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233813 | |||||||
| chr2:85233827 | C | T | 1 | a0002c0002t0002g0020 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.442-49668C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233827 | |||||||
| chr2:85233917 | C | T | 80 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(77): Show |
80 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(77): Show |
intron_variant | MODIFIER | c.442-49578C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233917 | |||||||
| chr2:85233943 | G | A | 1 | a0002c0002t0002g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.442-49552G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85233943 | |||||||
| chr2:85234020 | TA | T | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-49472delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234020 | ||||||
| chr2:85234094 | C | G | 35 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(32): Show |
35 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.442-49401C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234094 | |||||||
| chr2:85234131 | C | CT | 14 | a0001c0001t0001g0014 a0001c0001t0001g0096 a0001c0001t0001g0120 others(11): Show |
14 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-49342dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234131 | ||||||
| chr2:85234131 | CT | C | 68 | a0001c0001t0001g0090 a0001c0001t0001g0112 a0001c0001t0001g0136 others(65): Show |
68 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.442-49342delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234131 | ||||||
| chr2:85234131 | CTT | C | 15 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0002g0200 others(12): Show |
15 | HG01167.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-49343_442-4934 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85234131 | ||||||
| chr2:85234153 | T | C | 18 | a0001c0001t0001g0123 a0001c0001t0001g0151 a0001c0001t0001g0153 others(15): Show |
18 | HG00741.hp1 HG01109.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-49342T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234153 | |||||||
| chr2:85234236 | G | A | 41 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(38): Show |
41 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.442-49259G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234236 | |||||||
| chr2:85234709 | A | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48786A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234709 | |||||||
| chr2:85234733 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48762C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234733 | |||||||
| chr2:85234886 | T | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48609T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234886 | |||||||
| chr2:85234888 | G | T | 1 | a0001c0001t0002g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.442-48607G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85234888 | |||||||
| chr2:85235124 | A | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48371A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235124 | |||||||
| chr2:85235125 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-48370G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235125 | |||||||
| chr2:85235479 | C | T | 54 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0111 others(51): Show |
54 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.442-48016C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235479 | |||||||
| chr2:85235639 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(4): Show |
7 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-47856G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235639 | |||||||
| chr2:85235650 | G | A | 54 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0111 others(51): Show |
54 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.442-47845G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235650 | |||||||
| chr2:85235888 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-47607T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85235888 | |||||||
| chr2:85235995 | C | CA | 7 | a0001c0001t0001g0209 a0001c0001t0001g0234 a0002c0002t0002g0017 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-47492dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85235995 | ||||||
| chr2:85236015 | G | A | 10 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(7): Show |
10 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-47480G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236015 | |||||||
| chr2:85236046 | G | A | 10 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(7): Show |
10 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-47449G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236046 | |||||||
| chr2:85236172 | C | CT | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-47323_442-4732 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236172 | |||||||
| chr2:85236173 | C | CA | 81 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(78): Show |
81 | HG01071.hp2 HG01109.hp1 HG01167.hp2 others(78): Show |
intron_variant | MODIFIER | c.442-47314dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85236173 | ||||||
| chr2:85236176 | A | AT | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-47319_442-4731 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236176 | |||||||
| chr2:85236176 | A | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-47319A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236176 | |||||||
| chr2:85236259 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-47236T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236259 | |||||||
| chr2:85236386 | G | A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01256.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-47109G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236386 | |||||||
| chr2:85236662 | C | T | 1 | a0002c0002t0003g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.442-46833C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236662 | |||||||
| chr2:85236705 | A | G | 1 | a0003c0004t0002g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.442-46790A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236705 | |||||||
| chr2:85236850 | C | G | 1 | a0001c0001t0011g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.442-46645C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85236850 | |||||||
| chr2:85237032 | C | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0221 a0002c0002t0002g0065 |
3 | HG01934.hp2 HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.442-46463C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237032 | |||||||
| chr2:85237131 | G | A | 6 | a0001c0001t0001g0209 a0001c0001t0001g0234 a0002c0002t0002g0017 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-46364G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237131 | |||||||
| chr2:85237179 | T | A | 1 | a0002c0002t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.442-46316T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237179 | |||||||
| chr2:85237188 | A | G | 1 | a0008c0015t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442-46307A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237188 | |||||||
| chr2:85237370 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-46125G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237370 | |||||||
| chr2:85237403 | C | T | 1 | a0008c0015t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442-46092C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237403 | |||||||
| chr2:85237416 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.442-46079C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237416 | |||||||
| chr2:85237469 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.442-46026A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237469 | |||||||
| chr2:85237553 | A | G | 7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(4): Show |
7 | HG01256.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-45942A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237553 | |||||||
| chr2:85237559 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-45936C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237559 | |||||||
| chr2:85237795 | C | A | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-45700C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237795 | |||||||
| chr2:85237880 | T | C | 2 | a0002c0003t0002g0188 a0002c0007t0002g0029 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-45615T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237880 | |||||||
| chr2:85237903 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.442-45592C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85237903 | |||||||
| chr2:85238012 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-45483C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238012 | |||||||
| chr2:85238108 | G | GCC | 22 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(19): Show |
22 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-45385_442-4538 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238108 | ||||||
| chr2:85238127 | G | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-45368G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238127 | |||||||
| chr2:85238408 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-45087G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238408 | |||||||
| chr2:85238648 | A | T | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.442-44847A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238648 | |||||||
| chr2:85238652 | G | A | 1 | a0002c0003t0002g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.442-44843G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238652 | |||||||
| chr2:85238708 | G | A | 2 | a0001c0001t0001g0076 a0002c0002t0003g0075 |
2 | NA18950.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.442-44787G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85238708 | |||||||
| chr2:85238777 | TTTTA | T | 81 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0092 others(78): Show |
81 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.442-44666_442-4466 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | ||||||
| chr2:85238777 | TTTTATTT others(1): Show |
T | 96 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0091 others(93): Show |
96 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.442-44670_442-4466 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | ||||||
| chr2:85238777 | TTTTATTT others(5): Show |
T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0209 others(7): Show |
10 | HG01071.hp1 HG01175.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-44674_442-4466 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | ||||||
| chr2:85238777 | TTTTATTT others(9): Show |
T | 3 | a0001c0001t0001g0153 a0002c0002t0001g0069 a0002c0002t0001g0081 |
3 | HG01975.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-44678_442-4466 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | ||||||
| chr2:85238777 | TTTTATTT others(13): Show |
T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-44682_442-4466 others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | ||||||
| chr2:85238777 | TTTTATTT others(17): Show |
T | 33 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(30): Show |
33 | HG01934.hp2 HG02056.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.442-44686_442-4466 others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85238777 | ||||||
| chr2:85239152 | T | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-44343T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239152 | |||||||
| chr2:85239155 | A | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-44340A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239155 | |||||||
| chr2:85239159 | T | C | 3 | a0001c0001t0001g0015 a0002c0002t0001g0168 a0002c0002t0001g0172 |
3 | NA18950.hp2 NA19000.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.442-44336T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239159 | |||||||
| chr2:85239199 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.442-44296C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239199 | |||||||
| chr2:85239257 | T | C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-44238T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239257 | |||||||
| chr2:85239277 | G | A | 2 | a0001c0001t0002g0105 a0001c0016t0001g0203 |
2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-44218G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239277 | |||||||
| chr2:85239664 | C | G | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-43831C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239664 | |||||||
| chr2:85239725 | T | C | 1 | a0002c0010t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.442-43770T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239725 | |||||||
| chr2:85239741 | G | A | 34 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(31): Show |
34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-43754G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239741 | |||||||
| chr2:85239762 | A | G | 121 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(118): Show |
121 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(118): Show |
intron_variant | MODIFIER | c.442-43733A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239762 | |||||||
| chr2:85239802 | G | A | 34 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(31): Show |
34 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-43693G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239802 | |||||||
| chr2:85239807 | T | C | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-43688T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239807 | |||||||
| chr2:85239828 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.442-43667C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239828 | |||||||
| chr2:85239901 | G | A | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0002c0002t0002g0058 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-43594G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239901 | |||||||
| chr2:85239933 | G | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-43562G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239933 | |||||||
| chr2:85239944 | T | TA | 6 | a0001c0001t0002g0207 a0002c0002t0001g0040 a0002c0002t0001g0089 others(3): Show |
6 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-43534dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85239944 | ||||||
| chr2:85239944 | TA | T | 171 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0090 others(168): Show |
171 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(168): Show |
intron_variant | MODIFIER | c.442-43534delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85239944 | ||||||
| chr2:85239958 | A | C | 4 | a0001c0001t0001g0149 a0001c0001t0002g0105 a0002c0009t0001g0019 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-43537A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239958 | |||||||
| chr2:85239961 | AC | A | 5 | a0001c0001t0001g0170 a0001c0001t0001g0209 a0001c0001t0001g0234 others(2): Show |
5 | HG01175.hp2 HG01256.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-43533delC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239961 | |||||||
| chr2:85239962 | C | A | 16 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(13): Show |
16 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-43533C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85239962 | |||||||
| chr2:85240124 | G | A | 1 | a0002c0002t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.442-43371G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240124 | |||||||
| chr2:85240316 | G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-43179G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240316 | |||||||
| chr2:85240335 | G | T | 2 | a0002c0002t0001g0089 a0002c0002t0002g0043 |
2 | HG01109.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.442-43160G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240335 | |||||||
| chr2:85240418 | C | G | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-43077C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240418 | |||||||
| chr2:85240541 | G | T | 4 | a0001c0001t0001g0209 a0002c0002t0002g0018 a0002c0003t0002g0086 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-42954G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240541 | |||||||
| chr2:85240551 | C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-42944C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240551 | |||||||
| chr2:85240617 | C | CA | 76 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(73): Show |
76 | HG00735.hp1 HG00741.hp2 HG01109.hp1 others(73): Show |
intron_variant | MODIFIER | c.442-42862dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240617 | ||||||
| chr2:85240617 | C | CAA | 9 | a0001c0001t0001g0149 a0001c0001t0002g0105 a0001c0001t0002g0206 others(6): Show |
9 | HG01243.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-42863_442-4286 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240617 | ||||||
| chr2:85240732 | C | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(2): Show |
5 | HG03041.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-42763C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240732 | |||||||
| chr2:85240752 | G | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-42743G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240752 | |||||||
| chr2:85240776 | C | CA | 42 | a0001c0001t0001g0014 a0001c0001t0001g0090 a0001c0001t0001g0113 others(39): Show |
42 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.442-42700dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240776 | ||||||
| chr2:85240776 | C | CAA | 28 | a0001c0001t0001g0031 a0001c0001t0001g0156 a0001c0001t0001g0161 others(25): Show |
28 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-42701_442-4270 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85240776 | ||||||
| chr2:85240879 | G | A | 35 | a0001c0001t0001g0031 a0001c0001t0001g0156 a0001c0001t0001g0161 others(32): Show |
35 | HG01071.hp2 HG01109.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.442-42616G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240879 | |||||||
| chr2:85240933 | T | G | 5 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-42562T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240933 | |||||||
| chr2:85240995 | T | A | 2 | a0001c0001t0002g0181 a0002c0002t0001g0109 |
2 | NA18959.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.442-42500T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85240995 | |||||||
| chr2:85241431 | G | GTT | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.442-42060_442-4205 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | ||||||
| chr2:85241431 | G | GTTTT | 4 | a0001c0001t0001g0190 a0002c0002t0001g0038 a0002c0002t0001g0042 others(1): Show |
4 | HG01071.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-42062_442-4205 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | ||||||
| chr2:85241431 | G | GTTTTT | 7 | a0001c0001t0001g0156 a0002c0002t0001g0024 a0002c0002t0001g0040 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-42063_442-4205 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | ||||||
| chr2:85241431 | GTTTTTGT others(3): Show |
G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0161 a0001c0001t0001g0163 others(9): Show |
12 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-42058_442-4204 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | ||||||
| chr2:85241431 | GTTTTTGT others(5): Show |
G | 2 | a0001c0001t0002g0103 a0002c0002t0001g0051 |
2 | HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-42058_442-4204 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | ||||||
| chr2:85241431 | GTTTTTGT others(6): Show |
G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(1): Show |
4 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-42058_442-4204 others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241431 | ||||||
| chr2:85241437 | G | GT | 30 | a0001c0001t0001g0076 a0001c0001t0001g0095 a0001c0001t0001g0099 others(27): Show |
30 | HG00597.hp1 HG00621.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.442-42030dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241437 | ||||||
| chr2:85241437 | G | T | 16 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(13): Show |
16 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-42058G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241437 | |||||||
| chr2:85241437 | GT | G | 9 | a0001c0001t0001g0108 a0002c0002t0001g0062 a0002c0002t0001g0109 others(6): Show |
9 | HG00735.hp1 HG02132.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-42030delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241437 | ||||||
| chr2:85241437 | GTT | G | 46 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(43): Show |
46 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-42031_442-4203 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85241437 | ||||||
| chr2:85241439 | T | G | 3 | a0001c0001t0002g0167 a0001c0001t0002g0174 a0001c0001t0002g0175 |
3 | NA18967.hp2 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.442-42056T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241439 | |||||||
| chr2:85241443 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-42052T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241443 | |||||||
| chr2:85241448 | T | G | 4 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 others(1): Show |
4 | HG00735.hp1 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-42047T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241448 | |||||||
| chr2:85241449 | T | G | 44 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(41): Show |
44 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.442-42046T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241449 | |||||||
| chr2:85241455 | T | G | 12 | a0001c0001t0001g0031 a0001c0001t0001g0161 a0001c0001t0001g0163 others(9): Show |
12 | HG02572.hp2 HG02717.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-42040T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241455 | |||||||
| chr2:85241748 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-41747G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241748 | |||||||
| chr2:85241756 | T | G | 1 | a0001c0001t0002g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.442-41739T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241756 | |||||||
| chr2:85241928 | C | T | 3 | a0001c0001t0001g0209 a0002c0003t0002g0086 a0004c0012t0002g0184 |
3 | HG02572.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.442-41567C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85241928 | |||||||
| chr2:85242010 | G | T | 5 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 others(2): Show |
5 | HG00735.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-41485G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242010 | |||||||
| chr2:85242023 | C | CG | 179 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0088 others(176): Show |
179 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(176): Show |
intron_variant | MODIFIER | c.442-41465dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85242023 | ||||||
| chr2:85242123 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0122 |
2 | HG01074.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.442-41372T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242123 | |||||||
| chr2:85242244 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-41251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242244 | |||||||
| chr2:85242244 | TGG | T | 29 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(26): Show |
29 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-41249_442-4124 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85242244 | ||||||
| chr2:85242534 | T | G | 43 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(40): Show |
43 | HG00741.hp2 HG01167.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.442-40961T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242534 | |||||||
| chr2:85242866 | C | T | 13 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(10): Show |
13 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-40629C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242866 | |||||||
| chr2:85242895 | T | C | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.442-40600T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242895 | |||||||
| chr2:85242964 | A | G | 130 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(127): Show |
130 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(127): Show |
intron_variant | MODIFIER | c.442-40531A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242964 | |||||||
| chr2:85242974 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-40521A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242974 | |||||||
| chr2:85242982 | C | T | 47 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(44): Show |
47 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.442-40513C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85242982 | |||||||
| chr2:85243040 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-40455C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243040 | |||||||
| chr2:85243158 | G | A | 25 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(22): Show |
25 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-40337G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243158 | |||||||
| chr2:85243179 | A | G | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-40316A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243179 | |||||||
| chr2:85243276 | G | A | 25 | a0001c0001t0001g0031 a0001c0001t0001g0156 a0001c0001t0001g0161 others(22): Show |
25 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-40219G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243276 | |||||||
| chr2:85243300 | C | T | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-40195C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243300 | |||||||
| chr2:85243473 | AGGGGAAC others(19): Show |
A | 3 | a0001c0001t0002g0103 a0002c0002t0001g0050 a0002c0002t0001g0051 |
3 | HG01516.hp2 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-40015_442-3999 others(30): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85243473 | ||||||
| chr2:85243494 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-40001C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243494 | |||||||
| chr2:85243532 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.442-39963G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243532 | |||||||
| chr2:85243538 | G | A | 1 | a0002c0002t0001g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.442-39957G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243538 | |||||||
| chr2:85243659 | C | G | 9 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0002g0200 others(6): Show |
9 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-39836C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243659 | |||||||
| chr2:85243799 | A | G | 25 | a0001c0001t0001g0031 a0001c0001t0001g0156 a0001c0001t0001g0161 others(22): Show |
25 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-39696A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243799 | |||||||
| chr2:85243864 | A | G | 152 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(149): Show |
152 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(149): Show |
intron_variant | MODIFIER | c.442-39631A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243864 | |||||||
| chr2:85243935 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-39560C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243935 | |||||||
| chr2:85243971 | A | G | 4 | a0002c0002t0001g0062 a0002c0002t0002g0018 a0002c0002t0002g0061 others(1): Show |
4 | HG00735.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-39524A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85243971 | |||||||
| chr2:85244085 | C | G | 1 | a0006c0017t0001g0215 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.442-39410C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244085 | |||||||
| chr2:85244106 | G | C | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-39389G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244106 | |||||||
| chr2:85244336 | T | C | 59 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0097 others(56): Show |
59 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.442-39159T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244336 | |||||||
| chr2:85244513 | G | A | 6 | a0001c0001t0001g0209 a0001c0001t0002g0206 a0001c0001t0002g0207 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38982G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244513 | |||||||
| chr2:85244516 | AG | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38978delG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244516 | |||||||
| chr2:85244830 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.442-38665C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244830 | |||||||
| chr2:85244837 | A | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38658A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244837 | |||||||
| chr2:85244853 | A | G | 14 | a0001c0001t0001g0088 a0001c0001t0001g0199 a0001c0001t0001g0201 others(11): Show |
14 | HG01167.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-38642A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244853 | |||||||
| chr2:85244857 | G | A | 50 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0113 others(47): Show |
50 | HG00741.hp2 HG01168.hp1 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.442-38638G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244857 | |||||||
| chr2:85244932 | G | A | 39 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0001g0136 others(36): Show |
39 | HG00741.hp2 HG01168.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.442-38563G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244932 | |||||||
| chr2:85244965 | G | A | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-38530G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85244965 | |||||||
| chr2:85245039 | C | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-38456C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245039 | |||||||
| chr2:85245112 | C | T | 1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442-38383C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245112 | |||||||
| chr2:85245243 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.442-38252A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245243 | |||||||
| chr2:85245244 | T | C | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-38251T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245244 | |||||||
| chr2:85245475 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-38020T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245475 | |||||||
| chr2:85245529 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.442-37966C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245529 | |||||||
| chr2:85245833 | TA | T | 24 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0205 others(21): Show |
24 | HG01071.hp2 HG01109.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.442-37647delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85245833 | ||||||
| chr2:85245833 | TAA | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0170 a0001c0001t0001g0171 others(4): Show |
7 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-37648_442-3764 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85245833 | ||||||
| chr2:85245844 | A | C | 10 | a0001c0001t0001g0090 a0002c0002t0001g0007 a0002c0002t0001g0010 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-37651A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245844 | |||||||
| chr2:85245846 | A | C | 2 | a0001c0001t0001g0149 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-37649A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85245846 | |||||||
| chr2:85246057 | AATGC | A | 14 | a0001c0001t0001g0156 a0001c0001t0001g0190 a0001c0001t0001g0205 others(11): Show |
14 | HG01071.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-37436_442-3743 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85246057 | ||||||
| chr2:85246137 | C | A | 120 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(117): Show |
120 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(117): Show |
intron_variant | MODIFIER | c.442-37358C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85246137 | |||||||
| chr2:85246341 | G | C | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-37154G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85246341 | |||||||
| chr2:85246765 | AT | A | 36 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0092 others(33): Show |
36 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.442-36723delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85246765 | ||||||
| chr2:85247075 | A | C | 2 | a0002c0003t0002g0188 a0002c0007t0002g0029 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-36420A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247075 | |||||||
| chr2:85247086 | C | T | 1 | a0001c0001t0011g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.442-36409C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247086 | |||||||
| chr2:85247123 | T | C | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-36372T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247123 | |||||||
| chr2:85247160 | G | A | 36 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0092 others(33): Show |
36 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.442-36335G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247160 | |||||||
| chr2:85247217 | C | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-36278C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247217 | |||||||
| chr2:85247302 | C | T | 6 | a0001c0001t0002g0125 a0001c0001t0002g0167 a0001c0001t0002g0174 others(3): Show |
6 | HG01168.hp1 HG02080.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-36193C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247302 | |||||||
| chr2:85247309 | T | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-36186T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247309 | |||||||
| chr2:85247445 | A | C | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-36050A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247445 | |||||||
| chr2:85247684 | G | A | 2 | a0002c0002t0001g0069 a0002c0002t0001g0081 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-35811G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247684 | |||||||
| chr2:85247921 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0124 |
2 | NA18953.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.442-35574A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247921 | |||||||
| chr2:85247931 | C | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-35564C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247931 | |||||||
| chr2:85247951 | C | G | 1 | a0005c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.442-35544C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85247951 | |||||||
| chr2:85248274 | C | T | 45 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0092 others(42): Show |
45 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.442-35221C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248274 | |||||||
| chr2:85248580 | T | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0161 a0001c0001t0001g0163 others(8): Show |
11 | HG02572.hp2 HG02717.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-34915T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248580 | |||||||
| chr2:85248583 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-34912C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248583 | |||||||
| chr2:85248704 | T | C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-34791T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248704 | |||||||
| chr2:85248918 | C | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-34577C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85248918 | |||||||
| chr2:85249000 | G | GA | 44 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.442-34485dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85249000 | ||||||
| chr2:85249001 | A | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-34494A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249001 | |||||||
| chr2:85249057 | T | C | 210 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0076 others(207): Show |
210 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(207): Show |
intron_variant | MODIFIER | c.442-34438T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249057 | |||||||
| chr2:85249088 | T | G | 1 | a0002c0002t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.442-34407T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249088 | |||||||
| chr2:85249129 | G | A | 2 | a0001c0001t0001g0136 a0002c0002t0001g0034 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-34366G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249129 | |||||||
| chr2:85249435 | G | A | 4 | a0001c0001t0002g0103 a0002c0002t0001g0050 a0002c0002t0001g0051 others(1): Show |
4 | HG01175.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-34060G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249435 | |||||||
| chr2:85249653 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.442-33842C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249653 | |||||||
| chr2:85249758 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.442-33737G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85249758 | |||||||
| chr2:85250089 | A | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-33406A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250089 | |||||||
| chr2:85250290 | A | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-33205A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250290 | |||||||
| chr2:85250403 | T | A | 2 | a0002c0003t0002g0188 a0002c0007t0002g0029 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-33092T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250403 | |||||||
| chr2:85250403 | T | C | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-33092T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250403 | |||||||
| chr2:85250442 | A | AT | 44 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0092 others(41): Show |
44 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.442-33041dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85250442 | ||||||
| chr2:85250579 | G | A | 2 | a0002c0002t0001g0062 a0002c0002t0002g0061 |
2 | HG00735.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-32916G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250579 | |||||||
| chr2:85250594 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-32901G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250594 | |||||||
| chr2:85250597 | T | C | 134 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(131): Show |
134 | HG00597.hp1 HG00735.hp1 HG00735.hp2 others(131): Show |
intron_variant | MODIFIER | c.442-32898T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250597 | |||||||
| chr2:85250716 | G | T | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-32779G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250716 | |||||||
| chr2:85250912 | A | G | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-32583A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85250912 | |||||||
| chr2:85251126 | T | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0161 a0001c0001t0001g0163 others(7): Show |
10 | HG02572.hp2 HG02717.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-32369T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251126 | |||||||
| chr2:85251146 | GTTTAC | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(1): Show |
4 | HG03041.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-32346_442-3234 others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85251146 | ||||||
| chr2:85251191 | G | A | 3 | a0002c0002t0001g0062 a0002c0002t0002g0061 a0002c0002t0008g0059 |
3 | HG00735.hp1 HG02559.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.442-32304G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251191 | |||||||
| chr2:85251547 | C | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-31948C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251547 | |||||||
| chr2:85251788 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0219 |
2 | HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.442-31707C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251788 | |||||||
| chr2:85251790 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-31705A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251790 | |||||||
| chr2:85251883 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0006g0005 |
2 | HG00639.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.442-31612G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85251883 | |||||||
| chr2:85252007 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-31488C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252007 | |||||||
| chr2:85252101 | G | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-31394G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252101 | |||||||
| chr2:85252116 | T | G | 4 | a0001c0001t0002g0098 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | HG02258.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-31379T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252116 | |||||||
| chr2:85252117 | G | A | 13 | a0001c0001t0001g0126 a0001c0001t0001g0183 a0001c0001t0001g0222 others(10): Show |
13 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-31378G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252117 | |||||||
| chr2:85252179 | T | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-31316T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252179 | |||||||
| chr2:85252369 | T | G | 1 | a0005c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.442-31126T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252369 | |||||||
| chr2:85252602 | G | A | 2 | a0001c0001t0001g0149 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-30893G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252602 | |||||||
| chr2:85252603 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-30892C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252603 | |||||||
| chr2:85252825 | T | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0173 |
3 | HG01175.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-30670T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252825 | |||||||
| chr2:85252866 | A | C | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-30629A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252866 | |||||||
| chr2:85252888 | T | C | 62 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(59): Show |
62 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.442-30607T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252888 | |||||||
| chr2:85252984 | T | G | 56 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(53): Show |
56 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.442-30511T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85252984 | |||||||
| chr2:85253098 | T | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-30397T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253098 | |||||||
| chr2:85253112 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.442-30383C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253112 | |||||||
| chr2:85253141 | C | T | 1 | a0002c0002t0002g0066 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.442-30354C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253141 | |||||||
| chr2:85253299 | T | C | 39 | a0001c0001t0001g0088 a0001c0001t0001g0113 a0001c0001t0001g0149 others(36): Show |
39 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.442-30196T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253299 | |||||||
| chr2:85253302 | G | A | 61 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(58): Show |
61 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.442-30193G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253302 | |||||||
| chr2:85253341 | A | G | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-30154A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253341 | |||||||
| chr2:85253366 | G | A | 1 | a0002c0002t0001g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-30129G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253366 | |||||||
| chr2:85253413 | G | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0228 a0006c0017t0001g0215 |
3 | HG00280.hp1 HG01168.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.442-30082G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253413 | |||||||
| chr2:85253538 | G | A | 63 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(60): Show |
63 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.442-29957G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253538 | |||||||
| chr2:85253575 | T | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-29920T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253575 | |||||||
| chr2:85253592 | A | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(54): Show |
57 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.442-29903A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253592 | |||||||
| chr2:85253694 | T | G | 63 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(60): Show |
63 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.442-29801T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85253694 | |||||||
| chr2:85254066 | G | A | 1 | a0002c0002t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-29429G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254066 | |||||||
| chr2:85254226 | A | G | 11 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0001c0001t0002g0200 others(8): Show |
11 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-29269A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254226 | |||||||
| chr2:85254276 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-29219G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254276 | |||||||
| chr2:85254302 | C | T | 1 | a0002c0002t0003g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.442-29193C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254302 | |||||||
| chr2:85254401 | G | A | 57 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(54): Show |
57 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.442-29094G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254401 | |||||||
| chr2:85254427 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-29068G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254427 | |||||||
| chr2:85254443 | C | T | 9 | a0001c0001t0001g0031 a0001c0001t0001g0232 a0001c0001t0001g0234 others(6): Show |
9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-29052C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254443 | |||||||
| chr2:85254495 | G | A | 2 | a0002c0002t0001g0009 a0002c0002t0002g0016 |
2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.442-29000G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254495 | |||||||
| chr2:85254694 | C | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-28801C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254694 | |||||||
| chr2:85254946 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-28549G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254946 | |||||||
| chr2:85254984 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-28511C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85254984 | |||||||
| chr2:85255072 | T | C | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-28423T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255072 | |||||||
| chr2:85255092 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-28403G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255092 | |||||||
| chr2:85255120 | G | C | 11 | a0001c0001t0001g0090 a0001c0001t0002g0193 a0001c0001t0002g0200 others(8): Show |
11 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-28375G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255120 | |||||||
| chr2:85255226 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.442-28269C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255226 | |||||||
| chr2:85255246 | C | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-28249C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255246 | |||||||
| chr2:85255623 | G | A | 36 | a0001c0001t0001g0088 a0001c0001t0001g0113 a0001c0001t0001g0160 others(33): Show |
36 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.442-27872G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255623 | |||||||
| chr2:85255643 | C | G | 3 | a0001c0001t0001g0149 a0002c0002t0004g0085 a0009c0014t0002g0164 |
3 | HG02257.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.442-27852C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255643 | |||||||
| chr2:85255880 | G | A | 117 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(114): Show |
117 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.442-27615G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85255880 | |||||||
| chr2:85256022 | G | A | 40 | a0001c0001t0001g0088 a0001c0001t0001g0113 a0001c0001t0001g0149 others(37): Show |
40 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.442-27473G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256022 | |||||||
| chr2:85256118 | G | A | 2 | a0002c0002t0001g0042 a0002c0002t0002g0044 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.442-27377G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256118 | |||||||
| chr2:85256184 | T | C | 1 | a0004c0005t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.442-27311T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256184 | |||||||
| chr2:85256213 | C | G | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.442-27282C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256213 | |||||||
| chr2:85256214 | G | A | 2 | a0001c0001t0001g0179 a0002c0002t0003g0078 |
2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.442-27281G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256214 | |||||||
| chr2:85256227 | A | T | 102 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(99): Show |
102 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.442-27268A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256227 | |||||||
| chr2:85256258 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-27237G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256258 | |||||||
| chr2:85256273 | T | C | 17 | a0001c0001t0001g0113 a0001c0001t0001g0160 a0001c0001t0001g0197 others(14): Show |
17 | HG01074.hp2 HG01106.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-27222T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256273 | |||||||
| chr2:85256293 | G | A | 1 | a0002c0002t0002g0027 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.442-27202G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256293 | |||||||
| chr2:85256566 | A | G | 4 | a0001c0001t0002g0202 a0002c0002t0001g0062 a0002c0002t0002g0061 others(1): Show |
4 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-26929A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256566 | |||||||
| chr2:85256581 | G | T | 37 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(34): Show |
37 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-26914G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256581 | |||||||
| chr2:85256686 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0111 a0001c0001t0001g0128 others(5): Show |
8 | HG01074.hp1 HG01257.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-26809G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256686 | |||||||
| chr2:85256780 | T | A | 34 | a0001c0001t0001g0090 a0001c0001t0001g0099 a0001c0001t0001g0119 others(31): Show |
34 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.442-26715T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256780 | |||||||
| chr2:85256783 | G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-26712G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256783 | |||||||
| chr2:85256812 | A | G | 2 | a0001c0001t0001g0234 a0002c0002t0001g0033 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.442-26683A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85256812 | |||||||
| chr2:85256982 | T | TA | 116 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(113): Show |
116 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(113): Show |
intron_variant | MODIFIER | c.442-26501dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85256982 | ||||||
| chr2:85257396 | G | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0232 a0001c0001t0001g0234 others(6): Show |
9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-26099G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257396 | |||||||
| chr2:85257643 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-25852G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257643 | |||||||
| chr2:85257655 | G | GCCCTGCC others(3): Show |
9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-25834_442-2582 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85257655 | ||||||
| chr2:85257695 | G | A | 86 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0088 others(83): Show |
86 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.442-25800G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257695 | |||||||
| chr2:85257836 | C | T | 76 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(73): Show |
76 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.442-25659C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257836 | |||||||
| chr2:85257899 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.442-25596G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257899 | |||||||
| chr2:85257984 | T | C | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-25511T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85257984 | |||||||
| chr2:85258120 | G | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-25375G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258120 | |||||||
| chr2:85258139 | T | C | 1 | a0002c0003t0002g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.442-25356T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258139 | |||||||
| chr2:85258172 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.442-25323C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258172 | |||||||
| chr2:85258203 | T | C | 27 | a0001c0001t0001g0099 a0001c0001t0001g0119 a0001c0001t0001g0126 others(24): Show |
27 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-25292T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258203 | |||||||
| chr2:85258365 | C | T | 2 | a0001c0001t0002g0195 a0001c0016t0001g0203 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-25130C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258365 | |||||||
| chr2:85258395 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-25100T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258395 | |||||||
| chr2:85258457 | G | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-25038G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258457 | |||||||
| chr2:85258502 | A | G | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24993A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258502 | |||||||
| chr2:85258644 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-24851G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258644 | |||||||
| chr2:85258783 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.442-24712C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258783 | |||||||
| chr2:85258792 | G | A | 73 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(70): Show |
73 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.442-24703G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258792 | |||||||
| chr2:85258909 | C | T | 5 | a0001c0001t0001g0230 a0002c0002t0002g0018 a0002c0002t0002g0058 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-24586C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85258909 | |||||||
| chr2:85259019 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-24476C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259019 | |||||||
| chr2:85259039 | C | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(6): Show |
9 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-24456C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259039 | |||||||
| chr2:85259069 | C | G | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24426C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259069 | |||||||
| chr2:85259089 | T | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-24406T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259089 | |||||||
| chr2:85259107 | C | T | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24388C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259107 | |||||||
| chr2:85259194 | G | A | 4 | a0002c0003t0002g0086 a0004c0005t0001g0135 a0004c0005t0009g0204 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24301G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259194 | |||||||
| chr2:85259231 | T | G | 159 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(156): Show |
159 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.442-24264T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259231 | |||||||
| chr2:85259262 | C | T | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-24233C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259262 | |||||||
| chr2:85259430 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-24065C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259430 | |||||||
| chr2:85259449 | A | C | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-24046A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259449 | |||||||
| chr2:85259449 | A | G | 6 | a0001c0001t0001g0230 a0002c0002t0002g0018 a0002c0002t0002g0058 others(3): Show |
6 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-24046A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259449 | |||||||
| chr2:85259542 | T | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-23953T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259542 | |||||||
| chr2:85259556 | A | C | 4 | a0002c0003t0002g0086 a0004c0005t0001g0135 a0004c0005t0009g0204 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-23939A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259556 | |||||||
| chr2:85259579 | G | A | 3 | a0001c0001t0002g0103 a0002c0002t0001g0050 a0002c0002t0001g0051 |
3 | HG01516.hp2 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.442-23916G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259579 | |||||||
| chr2:85259830 | T | G | 2 | a0001c0001t0001g0149 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-23665T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259830 | |||||||
| chr2:85259853 | G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-23642G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259853 | |||||||
| chr2:85259999 | C | T | 5 | a0001c0001t0001g0097 a0001c0001t0001g0177 a0001c0001t0001g0187 others(2): Show |
5 | HG02523.hp1 NA18747.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-23496C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85259999 | |||||||
| chr2:85260033 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.442-23462G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260033 | |||||||
| chr2:85260034 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.442-23461C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260034 | |||||||
| chr2:85260107 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-23388G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260107 | |||||||
| chr2:85260291 | G | T | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-23204G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260291 | |||||||
| chr2:85260599 | G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-22896G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260599 | |||||||
| chr2:85260643 | C | CA | 72 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(69): Show |
72 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.442-22840dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85260643 | ||||||
| chr2:85260716 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-22779C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260716 | |||||||
| chr2:85260761 | G | A | 12 | a0001c0001t0001g0096 a0001c0001t0001g0123 a0001c0001t0001g0124 others(9): Show |
12 | HG00597.hp2 HG00741.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-22734G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85260761 | |||||||
| chr2:85261122 | T | TGG | 8 | a0001c0001t0001g0101 a0001c0001t0001g0111 a0001c0001t0001g0180 others(5): Show |
8 | HG01074.hp1 HG01168.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-22372_442-2237 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261122 | ||||||
| chr2:85261123 | G | GGT | 27 | a0001c0001t0001g0097 a0001c0001t0001g0113 a0001c0001t0001g0122 others(24): Show |
27 | HG00280.hp1 HG00738.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-22324_442-2232 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | G | GGTGT | 8 | a0001c0001t0001g0119 a0001c0001t0001g0138 a0001c0001t0001g0140 others(5): Show |
8 | HG01261.hp1 HG01891.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-22326_442-2232 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | G | GGTGTGT | 5 | a0001c0001t0001g0088 a0001c0001t0002g0102 a0001c0001t0002g0116 others(2): Show |
5 | HG01346.hp2 HG02886.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-22328_442-2232 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | GGT | G | 49 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0107 others(46): Show |
49 | HG00639.hp1 HG00639.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.442-22324_442-2232 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | GGTGT | G | 27 | a0001c0001t0001g0090 a0001c0001t0001g0149 a0001c0001t0001g0155 others(24): Show |
27 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-22326_442-2232 others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | GGTGTGT | G | 15 | a0001c0001t0001g0091 a0001c0001t0001g0131 a0001c0001t0001g0191 others(12): Show |
15 | HG00597.hp2 HG02080.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-22328_442-2232 others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | GGTGTGTG others(1): Show |
G | 15 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(12): Show |
15 | HG00735.hp1 HG01256.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-22330_442-2232 others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0001g0015 a0001c0001t0002g0105 a0002c0002t0003g0077 |
3 | HG02922.hp2 NA18950.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.442-22332_442-2232 others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | GGTGTGTG others(5): Show |
G | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0002t0001g0034 others(1): Show |
4 | HG02258.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-22334_442-2232 others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261123 | GGTGTGTG others(9): Show |
G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-22338_442-2232 others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261123 | ||||||
| chr2:85261125 | T | G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0092 others(19): Show |
22 | HG00597.hp1 HG00738.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.442-22370T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261125 | |||||||
| chr2:85261127 | T | G | 21 | a0001c0001t0001g0076 a0001c0001t0001g0107 a0001c0001t0001g0108 others(18): Show |
21 | HG00639.hp1 HG01071.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-22368T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261127 | |||||||
| chr2:85261129 | T | G | 6 | a0001c0001t0001g0223 a0001c0001t0002g0132 a0002c0002t0001g0025 others(3): Show |
6 | HG00735.hp2 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-22366T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261129 | |||||||
| chr2:85261131 | T | G | 13 | a0001c0001t0001g0091 a0001c0001t0001g0191 a0001c0001t0001g0218 others(10): Show |
13 | HG02080.hp1 HG02080.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-22364T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261131 | |||||||
| chr2:85261133 | T | G | 5 | a0001c0001t0002g0098 a0001c0001t0002g0125 a0001c0001t0007g0134 others(2): Show |
5 | HG01256.hp1 HG03098.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-22362T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261133 | |||||||
| chr2:85261135 | T | G | 1 | a0002c0002t0003g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.442-22360T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261135 | |||||||
| chr2:85261141 | T | G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-22354T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261141 | |||||||
| chr2:85261172 | G | GTGT | 3 | a0001c0001t0001g0133 a0001c0001t0001g0189 a0001c0001t0002g0210 |
3 | HG01243.hp1 HG02056.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.442-22323_442-2232 others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261172 | |||||||
| chr2:85261328 | A | T | 74 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(71): Show |
74 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.442-22167A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261328 | |||||||
| chr2:85261410 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0178 a0002c0002t0003g0068 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-22085C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261410 | |||||||
| chr2:85261420 | C | T | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-22075C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261420 | |||||||
| chr2:85261726 | TA | T | 65 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(62): Show |
65 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-21758delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85261726 | ||||||
| chr2:85261835 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-21660C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261835 | |||||||
| chr2:85261888 | G | T | 71 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(68): Show |
71 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.442-21607G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85261888 | |||||||
| chr2:85262157 | A | G | 78 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(75): Show |
78 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.442-21338A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262157 | |||||||
| chr2:85262174 | T | A | 74 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(71): Show |
74 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.442-21321T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262174 | |||||||
| chr2:85262268 | C | CT | 90 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(87): Show |
90 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.442-21227_442-2122 others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262268 | |||||||
| chr2:85262315 | G | C | 2 | a0001c0001t0001g0211 a0002c0002t0004g0055 |
2 | HG02056.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.442-21180G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262315 | |||||||
| chr2:85262392 | G | GA | 5 | a0001c0001t0001g0230 a0001c0001t0002g0195 a0001c0016t0001g0203 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-21090dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85262392 | ||||||
| chr2:85262392 | GA | G | 12 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0170 others(9): Show |
12 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-21090delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85262392 | ||||||
| chr2:85262524 | A | G | 3 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-20971A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262524 | |||||||
| chr2:85262895 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0187 a0001c0001t0001g0189 |
3 | NA18747.hp1 NA18943.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.442-20600A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262895 | |||||||
| chr2:85262989 | T | A | 54 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(51): Show |
54 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.442-20506T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85262989 | |||||||
| chr2:85263044 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-20451G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263044 | |||||||
| chr2:85263170 | C | T | 1 | a0002c0002t0003g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.442-20325C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263170 | |||||||
| chr2:85263299 | T | C | 5 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0002t0004g0085 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-20196T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263299 | |||||||
| chr2:85263319 | A | AG | 55 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(52): Show |
55 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.442-20169dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85263319 | ||||||
| chr2:85263853 | C | T | 6 | a0001c0001t0001g0149 a0001c0001t0002g0206 a0001c0001t0002g0207 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-19642C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263853 | |||||||
| chr2:85263854 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.442-19641G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263854 | |||||||
| chr2:85263881 | C | T | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-19614C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85263881 | |||||||
| chr2:85264103 | G | T | 1 | a0002c0002t0003g0079 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.442-19392G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264103 | |||||||
| chr2:85264113 | A | G | 3 | a0001c0001t0001g0199 a0002c0002t0007g0006 a0002c0010t0001g0186 |
3 | HG02965.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.442-19382A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264113 | |||||||
| chr2:85264130 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-19365C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264130 | |||||||
| chr2:85264242 | T | C | 56 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(53): Show |
56 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.442-19253T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264242 | |||||||
| chr2:85264277 | C | CA | 2 | a0002c0002t0001g0093 a0002c0002t0001g0094 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.442-19217dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85264277 | ||||||
| chr2:85264297 | T | C | 88 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(85): Show |
88 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.442-19198T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264297 | |||||||
| chr2:85264551 | C | T | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-18944C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264551 | |||||||
| chr2:85264559 | A | G | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-18936A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264559 | |||||||
| chr2:85264624 | T | C | 62 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(59): Show |
62 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.442-18871T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264624 | |||||||
| chr2:85264647 | G | A | 88 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(85): Show |
88 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.442-18848G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264647 | |||||||
| chr2:85264744 | A | ATT | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-18750_442-1874 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85264744 | ||||||
| chr2:85264803 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442-18692C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85264803 | |||||||
| chr2:85265018 | C | T | 89 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(86): Show |
89 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.442-18477C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265018 | |||||||
| chr2:85265032 | G | A | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-18463G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265032 | |||||||
| chr2:85265268 | G | T | 88 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(85): Show |
88 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.442-18227G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265268 | |||||||
| chr2:85265292 | T | TA | 85 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(82): Show |
85 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.442-18190dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85265292 | ||||||
| chr2:85265484 | C | G | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-18011C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265484 | |||||||
| chr2:85265596 | G | A | 1 | a0002c0002t0007g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-17899G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265596 | |||||||
| chr2:85265766 | G | GTT | 10 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(7): Show |
10 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-17718_442-1771 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85265766 | ||||||
| chr2:85265791 | A | G | 1 | a0002c0002t0001g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.442-17704A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265791 | |||||||
| chr2:85265879 | A | C | 88 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(85): Show |
88 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.442-17616A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85265879 | |||||||
| chr2:85266197 | G | A | 1 | a0001c0001t0002g0118 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.442-17298G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266197 | |||||||
| chr2:85266313 | A | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-17182A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266313 | |||||||
| chr2:85266446 | C | T | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-17049C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266446 | |||||||
| chr2:85266586 | T | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-16909T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266586 | |||||||
| chr2:85266596 | C | T | 2 | a0001c0001t0002g0195 a0001c0016t0001g0203 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-16899C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266596 | |||||||
| chr2:85266606 | C | T | 5 | a0001c0001t0002g0202 a0002c0002t0001g0062 a0002c0002t0002g0061 others(2): Show |
5 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-16889C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266606 | |||||||
| chr2:85266642 | T | G | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-16853T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266642 | |||||||
| chr2:85266952 | C | T | 1 | a0007c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.442-16543C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266952 | |||||||
| chr2:85266986 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-16509G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85266986 | |||||||
| chr2:85267190 | A | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-16305A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267190 | |||||||
| chr2:85267198 | G | A | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-16297G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267198 | |||||||
| chr2:85267263 | G | A | 47 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(44): Show |
47 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.442-16232G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267263 | |||||||
| chr2:85267292 | C | T | 5 | a0001c0001t0001g0230 a0002c0002t0002g0018 a0002c0002t0002g0058 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-16203C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267292 | |||||||
| chr2:85267330 | C | CA | 15 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0155 others(12): Show |
15 | HG01175.hp1 HG02080.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-16142dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267330 | ||||||
| chr2:85267330 | CA | C | 11 | a0001c0001t0001g0108 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
11 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-16142delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267330 | ||||||
| chr2:85267474 | C | A | 5 | a0001c0001t0001g0230 a0002c0002t0002g0018 a0002c0002t0002g0058 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-16021C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267474 | |||||||
| chr2:85267649 | C | CA | 58 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(55): Show |
58 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.442-15828dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267649 | ||||||
| chr2:85267649 | CA | C | 15 | a0001c0001t0001g0230 a0001c0001t0002g0129 a0002c0002t0001g0051 others(12): Show |
15 | HG01074.hp2 HG01517.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-15828delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85267649 | ||||||
| chr2:85267760 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-15735C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85267760 | |||||||
| chr2:85268135 | A | G | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-15360A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268135 | |||||||
| chr2:85268213 | G | T | 4 | a0002c0003t0002g0086 a0004c0005t0001g0135 a0004c0005t0009g0204 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-15282G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268213 | |||||||
| chr2:85268370 | G | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-15125G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268370 | |||||||
| chr2:85268471 | C | CTT | 45 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(42): Show |
45 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.442-15006_442-1500 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268471 | ||||||
| chr2:85268471 | CT | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-15005delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268471 | ||||||
| chr2:85268472 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0002g0196 |
2 | HG02257.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.442-15023T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268472 | |||||||
| chr2:85268536 | C | T | 16 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0163 others(13): Show |
16 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-14959C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268536 | |||||||
| chr2:85268621 | T | C | 1 | a0002c0002t0003g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.442-14874T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268621 | |||||||
| chr2:85268661 | C | T | 16 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0163 others(13): Show |
16 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-14834C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268661 | |||||||
| chr2:85268712 | G | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-14783G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268712 | |||||||
| chr2:85268732 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-14763G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268732 | |||||||
| chr2:85268759 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-14736C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268759 | |||||||
| chr2:85268767 | TA | T | 148 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(145): Show |
148 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.442-14711delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268767 | ||||||
| chr2:85268767 | TAA | T | 10 | a0001c0001t0001g0230 a0001c0001t0002g0206 a0001c0001t0002g0207 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-14712_442-1471 others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85268767 | ||||||
| chr2:85268808 | G | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-14687G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268808 | |||||||
| chr2:85268862 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-14633G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268862 | |||||||
| chr2:85268950 | T | C | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-14545T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268950 | |||||||
| chr2:85268976 | T | C | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-14519T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85268976 | |||||||
| chr2:85269011 | A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-14484A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269011 | |||||||
| chr2:85269032 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0002g0100 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.442-14463C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269032 | |||||||
| chr2:85269209 | G | A | 233 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(230): Show |
233 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(230): Show |
intron_variant | MODIFIER | c.442-14286G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269209 | |||||||
| chr2:85269229 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01891.hp2 HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.442-14266G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269229 | |||||||
| chr2:85269401 | C | T | 5 | a0001c0001t0001g0230 a0002c0002t0002g0018 a0002c0002t0002g0058 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-14094C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269401 | |||||||
| chr2:85269473 | A | G | 9 | a0001c0001t0001g0031 a0001c0001t0001g0232 a0001c0001t0001g0234 others(6): Show |
9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-14022A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269473 | |||||||
| chr2:85269587 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-13908C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269587 | |||||||
| chr2:85269716 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.442-13779T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269716 | |||||||
| chr2:85269815 | G | A | 1 | a0009c0014t0002g0164 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.442-13680G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269815 | |||||||
| chr2:85269838 | A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-13657A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269838 | |||||||
| chr2:85269881 | T | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0232 a0001c0001t0001g0234 others(6): Show |
9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-13614T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269881 | |||||||
| chr2:85269981 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-13514C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85269981 | |||||||
| chr2:85270015 | C | A | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.442-13480C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270015 | |||||||
| chr2:85270268 | C | T | 4 | a0001c0001t0002g0202 a0002c0002t0001g0062 a0002c0002t0002g0061 others(1): Show |
4 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-13227C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270268 | |||||||
| chr2:85270774 | C | T | 3 | a0001c0001t0002g0200 a0002c0002t0001g0037 a0002c0002t0003g0084 |
3 | HG01167.hp2 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.442-12721C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270774 | |||||||
| chr2:85270775 | G | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(5): Show |
8 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-12720G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270775 | |||||||
| chr2:85270777 | G | A | 77 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(74): Show |
77 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.442-12718G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270777 | |||||||
| chr2:85270781 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-12714G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270781 | |||||||
| chr2:85270933 | G | T | 2 | a0001c0001t0002g0098 a0002c0002t0004g0085 |
2 | HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.442-12562G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85270933 | |||||||
| chr2:85271065 | A | G | 4 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0188 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-12430A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271065 | |||||||
| chr2:85271098 | G | A | 3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0003t0002g0082 |
3 | HG02258.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-12397G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271098 | |||||||
| chr2:85271253 | C | T | 2 | a0001c0001t0002g0210 a0002c0002t0001g0013 |
2 | HG01243.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.442-12242C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271253 | |||||||
| chr2:85271287 | G | A | 11 | a0001c0001t0001g0230 a0001c0001t0002g0098 a0002c0002t0002g0018 others(8): Show |
11 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-12208G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271287 | |||||||
| chr2:85271370 | G | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0232 a0001c0001t0001g0234 others(6): Show |
9 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-12125G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271370 | |||||||
| chr2:85271660 | A | G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(59): Show |
62 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.442-11835A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271660 | |||||||
| chr2:85271763 | C | T | 38 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(35): Show |
38 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.442-11732C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271763 | |||||||
| chr2:85271797 | C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-11698C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271797 | |||||||
| chr2:85271845 | G | A | 76 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(73): Show |
76 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.442-11650G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85271845 | |||||||
| chr2:85272016 | G | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-11479G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272016 | |||||||
| chr2:85272043 | C | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-11452C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272043 | |||||||
| chr2:85272064 | C | A | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-11431C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272064 | |||||||
| chr2:85272070 | C | T | 1 | a0002c0002t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.442-11425C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272070 | |||||||
| chr2:85272109 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.442-11386G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272109 | |||||||
| chr2:85272413 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0206 a0001c0001t0002g0207 |
3 | HG02258.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442-11082C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272413 | |||||||
| chr2:85272439 | C | T | 72 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(69): Show |
72 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.442-11056C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272439 | |||||||
| chr2:85272519 | G | A | 64 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(61): Show |
64 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-10976G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272519 | |||||||
| chr2:85272631 | C | CA | 21 | a0001c0001t0001g0099 a0001c0001t0001g0126 a0001c0001t0001g0145 others(18): Show |
21 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-10850dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85272631 | ||||||
| chr2:85272631 | CA | C | 7 | a0001c0001t0001g0119 a0001c0001t0001g0214 a0001c0001t0001g0228 others(4): Show |
7 | HG00280.hp1 HG01168.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-10850delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85272631 | ||||||
| chr2:85272903 | T | C | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-10592T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272903 | |||||||
| chr2:85272997 | A | C | 1 | a0002c0002t0001g0117 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.442-10498A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85272997 | |||||||
| chr2:85273020 | G | A | 1 | a0002c0002t0003g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.442-10475G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273020 | |||||||
| chr2:85273029 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-10466C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273029 | |||||||
| chr2:85273128 | A | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-10367A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273128 | |||||||
| chr2:85273155 | A | G | 93 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(90): Show |
93 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.442-10340A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273155 | |||||||
| chr2:85273269 | A | T | 5 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0002c0003t0002g0036 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-10226A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273269 | |||||||
| chr2:85273326 | C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-10169C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273326 | |||||||
| chr2:85273466 | G | T | 3 | a0001c0001t0001g0136 a0002c0002t0001g0089 a0002c0002t0002g0043 |
3 | HG01109.hp1 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-10029G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273466 | |||||||
| chr2:85273595 | T | G | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.442-9900T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273595 | |||||||
| chr2:85273743 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-9752G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273743 | |||||||
| chr2:85273826 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-9669C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273826 | |||||||
| chr2:85273838 | G | A | 15 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0163 others(12): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-9657G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273838 | |||||||
| chr2:85273950 | G | A | 71 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(68): Show |
71 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.442-9545G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85273950 | |||||||
| chr2:85274031 | G | A | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-9464G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274031 | |||||||
| chr2:85274058 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442-9437G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274058 | |||||||
| chr2:85274242 | C | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-9253C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274242 | |||||||
| chr2:85274261 | C | A | 65 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(62): Show |
65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-9234C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274261 | |||||||
| chr2:85274267 | G | A | 65 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(62): Show |
65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-9228G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274267 | |||||||
| chr2:85274286 | C | T | 65 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(62): Show |
65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-9209C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274286 | |||||||
| chr2:85274290 | C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-9205C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274290 | |||||||
| chr2:85274342 | G | A | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-9153G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274342 | |||||||
| chr2:85274344 | G | C | 66 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(63): Show |
66 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.442-9151G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274344 | |||||||
| chr2:85274583 | A | G | 5 | a0002c0003t0002g0082 a0002c0003t0002g0086 a0004c0005t0001g0135 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8912A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274583 | |||||||
| chr2:85274636 | G | A | 5 | a0002c0003t0002g0082 a0002c0003t0002g0086 a0004c0005t0001g0135 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8859G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274636 | |||||||
| chr2:85274876 | G | A | 66 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(63): Show |
66 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.442-8619G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274876 | |||||||
| chr2:85274908 | T | G | 5 | a0002c0003t0002g0082 a0002c0003t0002g0086 a0004c0005t0001g0135 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8587T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85274908 | |||||||
| chr2:85275093 | C | G | 1 | a0002c0002t0003g0146 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.442-8402C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275093 | |||||||
| chr2:85275113 | G | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(45): Show |
48 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.442-8382G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275113 | |||||||
| chr2:85275141 | A | C | 216 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(213): Show |
216 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(213): Show |
intron_variant | MODIFIER | c.442-8354A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275141 | |||||||
| chr2:85275176 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.442-8319C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275176 | |||||||
| chr2:85275296 | G | A | 118 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(115): Show |
118 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.442-8199G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275296 | |||||||
| chr2:85275312 | C | T | 5 | a0002c0003t0002g0082 a0002c0003t0002g0086 a0004c0005t0001g0135 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8183C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275312 | |||||||
| chr2:85275641 | G | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.442-7854G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275641 | |||||||
| chr2:85275919 | C | CA | 39 | a0001c0001t0001g0090 a0001c0001t0001g0099 a0001c0001t0001g0113 others(36): Show |
39 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.442-7558dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | ||||||
| chr2:85275919 | C | CAA | 71 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(68): Show |
71 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.442-7559_442-7558d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | ||||||
| chr2:85275919 | C | CAAA | 65 | a0001c0001t0001g0015 a0001c0001t0001g0091 a0001c0001t0001g0097 others(62): Show |
65 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-7560_442-7558d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | ||||||
| chr2:85275919 | C | CAAAA | 10 | a0001c0001t0001g0119 a0001c0001t0001g0136 a0001c0001t0001g0155 others(7): Show |
10 | HG00280.hp1 HG01168.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-7561_442-7558d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85275919 | ||||||
| chr2:85275938 | T | A | 28 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0123 others(25): Show |
28 | HG00741.hp1 HG01891.hp2 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-7557T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85275938 | |||||||
| chr2:85276016 | G | T | 47 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(44): Show |
47 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.442-7479G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276016 | |||||||
| chr2:85276070 | C | G | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0103 others(3): Show |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-7425C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276070 | |||||||
| chr2:85276289 | T | C | 3 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-7206T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276289 | |||||||
| chr2:85276413 | G | A | 2 | a0001c0001t0001g0178 a0002c0002t0003g0079 |
2 | NA18966.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.442-7082G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276413 | |||||||
| chr2:85276445 | A | C | 71 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(68): Show |
71 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.442-7050A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276445 | |||||||
| chr2:85276551 | A | C | 64 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(61): Show |
64 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-6944A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276551 | |||||||
| chr2:85276588 | C | T | 3 | a0001c0001t0001g0136 a0002c0002t0001g0089 a0002c0002t0002g0043 |
3 | HG01109.hp1 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.442-6907C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276588 | |||||||
| chr2:85276723 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.442-6772A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276723 | |||||||
| chr2:85276873 | A | G | 154 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(151): Show |
154 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.442-6622A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85276873 | |||||||
| chr2:85277068 | G | A | 64 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(61): Show |
64 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.442-6427G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277068 | |||||||
| chr2:85277309 | G | A | 5 | a0002c0003t0002g0082 a0002c0003t0002g0086 a0004c0005t0001g0135 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-6186G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277309 | |||||||
| chr2:85277372 | A | G | 2 | a0001c0001t0001g0149 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.442-6123A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277372 | |||||||
| chr2:85277581 | G | A | 77 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(74): Show |
77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-5914G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277581 | |||||||
| chr2:85277743 | G | T | 15 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0163 others(12): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-5752G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277743 | |||||||
| chr2:85277754 | A | G | 77 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(74): Show |
77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-5741A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277754 | |||||||
| chr2:85277759 | A | G | 1 | a0002c0002t0003g0079 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.442-5736A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277759 | |||||||
| chr2:85277827 | G | A | 2 | a0001c0001t0001g0090 a0002c0002t0001g0030 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.442-5668G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277827 | |||||||
| chr2:85277866 | A | G | 133 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(130): Show |
133 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.442-5629A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277866 | |||||||
| chr2:85277882 | TAG | T | 3 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-5610_442-5609d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85277882 | ||||||
| chr2:85277984 | T | C | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442-5511T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277984 | |||||||
| chr2:85277992 | C | T | 1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-5503C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85277992 | |||||||
| chr2:85278138 | C | T | 2 | a0001c0001t0001g0179 a0002c0002t0003g0078 |
2 | HG02129.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.442-5357C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278138 | |||||||
| chr2:85278202 | C | T | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0002c0009t0001g0019 others(1): Show |
4 | HG02258.hp1 HG02895.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-5293C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278202 | |||||||
| chr2:85278257 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.442-5238G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278257 | |||||||
| chr2:85278346 | G | A | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.442-5149G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278346 | |||||||
| chr2:85278439 | T | C | 77 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(74): Show |
77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-5056T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278439 | |||||||
| chr2:85278479 | C | T | 17 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0001g0190 others(14): Show |
17 | HG01071.hp2 HG01074.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-5016C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278479 | |||||||
| chr2:85278588 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0002g0116 a0001c0001t0002g0118 others(1): Show |
4 | HG02056.hp1 NA18951.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-4907G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278588 | |||||||
| chr2:85278797 | C | T | 47 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(44): Show |
47 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.442-4698C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278797 | |||||||
| chr2:85278857 | T | A | 77 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(74): Show |
77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4638T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278857 | |||||||
| chr2:85278877 | G | A | 77 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(74): Show |
77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4618G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278877 | |||||||
| chr2:85278915 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.442-4580G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278915 | |||||||
| chr2:85278981 | G | A | 145 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(142): Show |
145 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(142): Show |
intron_variant | MODIFIER | c.442-4514G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85278981 | |||||||
| chr2:85279019 | C | T | 70 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(67): Show |
70 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.442-4476C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279019 | |||||||
| chr2:85279037 | G | A | 124 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(121): Show |
124 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.442-4458G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279037 | |||||||
| chr2:85279056 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-4439C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279056 | |||||||
| chr2:85279066 | GT | G | 15 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0163 others(12): Show |
15 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.442-4428delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279066 | |||||||
| chr2:85279140 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0006g0005 |
2 | HG00639.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.442-4355G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279140 | |||||||
| chr2:85279329 | C | T | 12 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0163 others(9): Show |
12 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-4166C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279329 | |||||||
| chr2:85279377 | A | ACGTT | 77 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(74): Show |
77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4118_442-4117i others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279377 | |||||||
| chr2:85279409 | AAAAT | A | 65 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(62): Show |
65 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-4074_442-4071d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85279409 | ||||||
| chr2:85279465 | T | C | 77 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(74): Show |
77 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-4030T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279465 | |||||||
| chr2:85279590 | C | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-3905C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279590 | |||||||
| chr2:85279668 | C | T | 5 | a0001c0001t0002g0202 a0002c0002t0001g0057 a0002c0002t0001g0062 others(2): Show |
5 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-3827C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279668 | |||||||
| chr2:85279712 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.442-3783A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279712 | |||||||
| chr2:85279970 | A | C | 2 | a0002c0003t0002g0036 a0002c0003t0002g0188 |
2 | HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.442-3525A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85279970 | |||||||
| chr2:85280095 | A | G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-3400A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280095 | |||||||
| chr2:85280211 | T | C | 124 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(121): Show |
124 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.442-3284T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280211 | |||||||
| chr2:85280220 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.442-3275T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280220 | |||||||
| chr2:85280526 | G | T | 3 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.442-2969G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280526 | |||||||
| chr2:85280534 | G | A | 70 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(67): Show |
70 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.442-2961G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280534 | |||||||
| chr2:85280665 | A | T | 70 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(67): Show |
70 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.442-2830A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280665 | |||||||
| chr2:85280823 | A | G | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-2672A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280823 | |||||||
| chr2:85280942 | C | A | 79 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0112 others(76): Show |
79 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.442-2553C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280942 | |||||||
| chr2:85280991 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0002g0067 a0002c0002t0012g0021 |
3 | HG02451.hp2 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.442-2504G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85280991 | |||||||
| chr2:85281020 | CT | C | 69 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0096 others(66): Show |
69 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-2454delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281020 | ||||||
| chr2:85281020 | CTT | C | 11 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0152 others(8): Show |
11 | HG01167.hp2 HG01243.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-2455_442-2454d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281020 | ||||||
| chr2:85281020 | CTTT | C | 134 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(131): Show |
134 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.442-2456_442-2454d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281020 | ||||||
| chr2:85281134 | C | T | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-2361C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281134 | |||||||
| chr2:85281147 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-2348C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281147 | |||||||
| chr2:85281180 | T | C | 151 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0076 others(148): Show |
151 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.442-2315T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281180 | |||||||
| chr2:85281213 | C | A | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.442-2282C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281213 | |||||||
| chr2:85281276 | T | C | 91 | a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0097 others(88): Show |
91 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.442-2219T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281276 | |||||||
| chr2:85281325 | A | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-2170A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281325 | |||||||
| chr2:85281331 | T | C | 93 | a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0097 others(90): Show |
93 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.442-2164T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281331 | |||||||
| chr2:85281497 | T | C | 1 | a0002c0002t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.442-1998T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281497 | |||||||
| chr2:85281702 | G | A | 98 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0095 others(95): Show |
98 | HG00280.hp2 HG00597.hp1 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.442-1793G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281702 | |||||||
| chr2:85281727 | G | A | 70 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(67): Show |
70 | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.442-1768G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281727 | |||||||
| chr2:85281847 | T | C | 7 | a0001c0001t0001g0123 a0001c0001t0001g0153 a0001c0001t0002g0181 others(4): Show |
7 | HG00741.hp1 HG01952.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1648T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281847 | |||||||
| chr2:85281932 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-1563T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85281932 | |||||||
| chr2:85281989 | C | CT | 84 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(81): Show |
84 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.442-1497dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85281989 | ||||||
| chr2:85282334 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-1161C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282334 | |||||||
| chr2:85282416 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.442-1079T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282416 | |||||||
| chr2:85282453 | A | G | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-1042A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282453 | |||||||
| chr2:85282468 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442-1027G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282468 | |||||||
| chr2:85282541 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-954G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282541 | |||||||
| chr2:85282690 | G | A | 12 | a0001c0001t0001g0126 a0001c0001t0001g0183 a0001c0001t0001g0222 others(9): Show |
12 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-805G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282690 | |||||||
| chr2:85282794 | T | TTG | 54 | a0001c0001t0001g0015 a0001c0001t0001g0090 a0001c0001t0001g0101 others(51): Show |
54 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.442-653_442-652dup others(2): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | T | TTGTG | 24 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0091 others(21): Show |
24 | HG00738.hp1 HG01074.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.442-655_442-652dup others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | T | TTGTGTG | 18 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0133 others(15): Show |
18 | HG00735.hp2 HG01257.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-657_442-652dup others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | T | TTGTGTGT others(1): Show |
22 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0140 others(19): Show |
22 | HG00597.hp2 HG00738.hp2 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.442-659_442-652dup others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | T | TTGTGTGT others(3): Show |
8 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0197 others(5): Show |
8 | HG01256.hp1 HG02080.hp1 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-661_442-652dup others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0121 others(2): Show |
5 | HG03139.hp2 HG03486.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-663_442-652dup others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | T | TTGTGTGT others(7): Show |
3 | a0001c0001t0001g0095 a0001c0001t0001g0163 a0005c0006t0002g0137 |
3 | HG00597.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.442-665_442-652dup others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTG | T | 13 | a0001c0001t0001g0113 a0001c0001t0001g0183 a0001c0001t0001g0228 others(10): Show |
13 | HG00280.hp1 HG00280.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-653_442-652del others(2): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTG | T | 15 | a0001c0001t0001g0126 a0001c0001t0001g0201 a0001c0001t0001g0222 others(12): Show |
15 | HG00741.hp2 HG01106.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-655_442-652del others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTGTG | T | 4 | a0001c0001t0002g0147 a0002c0002t0001g0050 a0002c0002t0001g0051 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-657_442-652del others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTGTGT others(1): Show |
T | 16 | a0001c0001t0001g0099 a0001c0001t0001g0145 a0001c0001t0001g0170 others(13): Show |
16 | HG00735.hp1 HG01175.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-659_442-652del others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0002g0127 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.442-661_442-652del others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0232 a0002c0002t0012g0021 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.442-663_442-652del others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-665_442-652del others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-673_442-652del others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282794 | TTGTGTGT others(21): Show |
T | 5 | a0002c0003t0002g0082 a0002c0003t0002g0086 a0004c0005t0001g0135 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-679_442-652del others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85282794 | ||||||
| chr2:85282895 | G | A | 76 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(73): Show |
76 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.442-600G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282895 | |||||||
| chr2:85282932 | A | G | 7 | a0002c0003t0002g0036 a0002c0003t0002g0082 a0002c0003t0002g0086 others(4): Show |
7 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-563A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282932 | |||||||
| chr2:85282970 | A | G | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-525A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85282970 | |||||||
| chr2:85283010 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.442-485C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283010 | |||||||
| chr2:85283102 | A | G | 1 | a0001c0001t0002g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.442-393A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283102 | |||||||
| chr2:85283172 | C | G | 56 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(53): Show |
56 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.442-323C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283172 | |||||||
| chr2:85283222 | G | A | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.442-273G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283222 | |||||||
| chr2:85283251 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0124 |
2 | NA18953.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.442-244A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283251 | |||||||
| chr2:85283261 | C | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-234C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283261 | |||||||
| chr2:85283265 | T | TCCC | 35 | a0001c0001t0001g0088 a0001c0001t0001g0099 a0001c0001t0001g0145 others(32): Show |
35 | HG00280.hp2 HG02056.hp2 HG02257.hp1 others(32): Show |
intron_variant | MODIFIER | c.442-222_442-220dup others(3): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85283265 | ||||||
| chr2:85283265 | T | TCCCC | 46 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0113 others(43): Show |
46 | HG01167.hp2 HG01358.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-223_442-220dup others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85283265 | ||||||
| chr2:85283271 | C | CCCG | 49 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(46): Show |
49 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.442-222_442-221ins others(3): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 85283271 | ||||||
| chr2:85283271 | C | CG | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-224_442-223ins others(1): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283271 | |||||||
| chr2:85283274 | C | G | 1 | a0002c0002t0001g0117 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.442-221C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283274 | |||||||
| chr2:85283277 | A | G | 56 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(53): Show |
56 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.442-218A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283277 | |||||||
| chr2:85283289 | G | A | 2 | a0001c0001t0002g0195 a0001c0016t0001g0203 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.442-206G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283289 | |||||||
| chr2:85283302 | G | A | 48 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(45): Show |
48 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.442-193G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283302 | |||||||
| chr2:85283337 | A | G | 1 | a0002c0002t0003g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.442-158A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283337 | |||||||
| chr2:85283341 | G | A | 1 | a0002c0002t0002g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442-154G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 3/11 | chr2 | 85283341 | |||||||
| chr2:85283654 | A | G | 148 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(145): Show |
148 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.525+76A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283654 | |||||||
| chr2:85283708 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+130G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283708 | |||||||
| chr2:85283802 | C | T | 1 | a0002c0002t0002g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525+224C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283802 | |||||||
| chr2:85283842 | A | G | 159 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(156): Show |
159 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(156): Show |
intron_variant | MODIFIER | c.525+264A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283842 | |||||||
| chr2:85283855 | C | T | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+277C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283855 | |||||||
| chr2:85283859 | C | T | 2 | a0001c0001t0007g0134 a0005c0006t0002g0137 |
2 | HG01256.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.525+281C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283859 | |||||||
| chr2:85283897 | G | A | 2 | a0001c0001t0002g0195 a0001c0016t0001g0203 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525+319G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283897 | |||||||
| chr2:85283898 | T | C | 92 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(89): Show |
92 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.525+320T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85283898 | |||||||
| chr2:85283992 | C | CTGTTTT | 2 | a0001c0001t0001g0201 a0002c0002t0001g0236 |
2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.525+438_525+443dup others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85283992 | ||||||
| chr2:85284357 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.525+779C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284357 | |||||||
| chr2:85284454 | C | G | 2 | a0001c0001t0001g0149 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.525+876C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284454 | |||||||
| chr2:85284471 | A | G | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+893A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284471 | |||||||
| chr2:85284477 | A | T | 2 | a0001c0001t0001g0149 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.525+899A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284477 | |||||||
| chr2:85284512 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.525+934A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284512 | |||||||
| chr2:85284514 | C | A | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.525+936C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284514 | |||||||
| chr2:85284523 | A | T | 27 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0123 others(24): Show |
27 | HG00741.hp1 HG01891.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.525+945A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284523 | |||||||
| chr2:85284639 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.525+1061G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284639 | |||||||
| chr2:85284707 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.525+1129A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284707 | |||||||
| chr2:85284939 | A | G | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+1361A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284939 | |||||||
| chr2:85284950 | A | C | 2 | a0001c0001t0001g0234 a0002c0002t0001g0033 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.525+1372A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284950 | |||||||
| chr2:85284972 | G | A | 11 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0211 others(8): Show |
11 | HG02056.hp2 HG02165.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.525+1394G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85284972 | |||||||
| chr2:85285016 | G | A | 4 | a0001c0001t0002g0098 a0001c0001t0002g0195 a0001c0016t0001g0203 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+1438G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285016 | |||||||
| chr2:85285032 | T | G | 2 | a0001c0001t0002g0195 a0001c0016t0001g0203 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.525+1454T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285032 | |||||||
| chr2:85285101 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.525+1523C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285101 | |||||||
| chr2:85285149 | T | C | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0105 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1571T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285149 | |||||||
| chr2:85285165 | G | A | 5 | a0001c0001t0002g0098 a0001c0001t0002g0195 a0001c0016t0001g0203 others(2): Show |
5 | HG02622.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+1587G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285165 | |||||||
| chr2:85285175 | G | A | 1 | a0002c0002t0001g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.525+1597G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285175 | |||||||
| chr2:85285232 | C | CA | 10 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0149 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1666dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85285232 | ||||||
| chr2:85285234 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.525+1656A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285234 | |||||||
| chr2:85285363 | T | C | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0105 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1785T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285363 | |||||||
| chr2:85285370 | G | A | 1 | a0003c0004t0002g0106 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.525+1792G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285370 | |||||||
| chr2:85285489 | T | TG | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0105 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1912dupG | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85285489 | ||||||
| chr2:85285505 | C | T | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0105 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1927C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285505 | |||||||
| chr2:85285552 | T | C | 152 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(149): Show |
152 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.525+1974T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285552 | |||||||
| chr2:85285611 | C | G | 1 | a0001c0001t0002g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.525+2033C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285611 | |||||||
| chr2:85285684 | G | A | 6 | a0001c0001t0002g0202 a0002c0002t0001g0057 a0002c0002t0001g0062 others(3): Show |
6 | HG00735.hp1 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+2106G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285684 | |||||||
| chr2:85285786 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.525+2208G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285786 | |||||||
| chr2:85285837 | T | C | 4 | a0001c0001t0002g0105 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | HG02258.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+2259T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285837 | |||||||
| chr2:85285838 | T | G | 152 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0076 others(149): Show |
152 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.525+2260T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285838 | |||||||
| chr2:85285844 | C | T | 2 | a0002c0002t0001g0034 a0002c0002t0002g0066 |
2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.525+2266C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285844 | |||||||
| chr2:85285856 | G | T | 8 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(5): Show |
8 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+2278G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285856 | |||||||
| chr2:85285901 | A | G | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0105 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+2323A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285901 | |||||||
| chr2:85285929 | C | T | 10 | a0001c0001t0001g0149 a0001c0001t0001g0230 a0001c0001t0002g0105 others(7): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+2351C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285929 | |||||||
| chr2:85285945 | A | C | 3 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525+2367A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85285945 | |||||||
| chr2:85286038 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.525+2460A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286038 | |||||||
| chr2:85286041 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.525+2463A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286041 | |||||||
| chr2:85286115 | C | T | 55 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0091 others(52): Show |
55 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.525+2537C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286115 | |||||||
| chr2:85286191 | C | CA | 17 | a0001c0001t0001g0124 a0001c0001t0001g0149 a0001c0001t0002g0098 others(14): Show |
17 | HG01952.hp1 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.525+2632dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85286191 | ||||||
| chr2:85286191 | CA | C | 5 | a0001c0001t0002g0202 a0001c0001t0011g0142 a0002c0002t0001g0062 others(2): Show |
5 | HG00735.hp1 HG01884.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+2632delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85286191 | ||||||
| chr2:85286363 | C | A | 90 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(87): Show |
90 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.525+2785C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286363 | |||||||
| chr2:85286370 | A | C | 84 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(81): Show |
84 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.525+2792A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286370 | |||||||
| chr2:85286371 | C | A | 81 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(78): Show |
81 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.525+2793C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286371 | |||||||
| chr2:85286373 | A | C | 47 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0096 others(44): Show |
47 | HG00741.hp1 HG01891.hp2 HG01952.hp1 others(44): Show |
intron_variant | MODIFIER | c.525+2795A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286373 | |||||||
| chr2:85286374 | A | AC | 10 | a0001c0001t0001g0149 a0001c0001t0002g0105 a0002c0002t0001g0057 others(7): Show |
10 | HG02257.hp1 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+2796_525+2797i others(3): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286374 | |||||||
| chr2:85286379 | A | G | 3 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525+2801A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286379 | |||||||
| chr2:85286387 | C | A | 3 | a0001c0001t0001g0230 a0002c0002t0002g0058 a0010c0011t0002g0231 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525+2809C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286387 | |||||||
| chr2:85286582 | G | A | 1 | a0002c0002t0003g0075 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.525+3004G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286582 | |||||||
| chr2:85286599 | G | C | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+3021G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286599 | |||||||
| chr2:85286681 | G | C | 77 | a0001c0001t0001g0031 a0001c0001t0001g0088 a0001c0001t0001g0090 others(74): Show |
77 | HG00280.hp2 HG00741.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.525+3103G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286681 | |||||||
| chr2:85286804 | A | T | 1 | a0003c0004t0002g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.525+3226A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286804 | |||||||
| chr2:85286935 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0005g0001 a0001c0001t0006g0003 others(1): Show |
4 | HG00741.hp2 HG01106.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+3357C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85286935 | |||||||
| chr2:85287001 | A | G | 25 | a0001c0001t0001g0099 a0001c0001t0001g0112 a0001c0001t0001g0126 others(22): Show |
25 | HG00280.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.525+3423A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287001 | |||||||
| chr2:85287059 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+3481G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287059 | |||||||
| chr2:85287110 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.525+3532C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287110 | |||||||
| chr2:85287139 | C | T | 9 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0131 others(6): Show |
9 | HG00597.hp2 HG02080.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+3561C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287139 | |||||||
| chr2:85287207 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0219 |
2 | HG02129.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.525+3629C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287207 | |||||||
| chr2:85287228 | T | A | 1 | a0002c0002t0001g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.525+3650T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287228 | |||||||
| chr2:85287453 | A | G | 22 | a0001c0001t0001g0088 a0001c0001t0001g0113 a0001c0001t0001g0149 others(19): Show |
22 | HG02056.hp2 HG02165.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.525+3875A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287453 | |||||||
| chr2:85287594 | A | G | 52 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0096 others(49): Show |
52 | HG00741.hp1 HG01167.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.525+4016A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287594 | |||||||
| chr2:85287809 | G | A | 29 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0123 others(26): Show |
29 | HG00741.hp1 HG01167.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.525+4231G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85287809 | |||||||
| chr2:85288020 | T | C | 5 | a0002c0003t0002g0082 a0002c0003t0002g0086 a0004c0005t0001g0135 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+4442T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288020 | |||||||
| chr2:85288415 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+4837G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288415 | |||||||
| chr2:85288620 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.525+5042T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288620 | |||||||
| chr2:85288653 | G | A | 1 | a0002c0002t0001g0007 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.525+5075G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288653 | |||||||
| chr2:85288870 | G | A | 1 | a0002c0002t0001g0056 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.525+5292G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288870 | |||||||
| chr2:85288967 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.525+5389G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85288967 | |||||||
| chr2:85289094 | C | A | 9 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0002c0002t0001g0050 others(6): Show |
9 | HG01106.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+5516C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289094 | |||||||
| chr2:85289194 | A | G | 19 | a0001c0001t0001g0088 a0001c0001t0001g0113 a0001c0001t0001g0197 others(16): Show |
19 | HG02056.hp2 HG02165.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.525+5616A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289194 | |||||||
| chr2:85289221 | A | AGT | 25 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0001t0001g0126 others(22): Show |
25 | HG00621.hp2 HG00741.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.525+5674_525+5675d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | ||||||
| chr2:85289221 | A | AGTGT | 48 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0092 others(45): Show |
48 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.525+5672_525+5675d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | ||||||
| chr2:85289221 | A | AGTGTGT | 9 | a0001c0001t0001g0230 a0001c0001t0002g0125 a0001c0001t0002g0167 others(6): Show |
9 | HG01243.hp1 HG02080.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.525+5670_525+5675d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | ||||||
| chr2:85289221 | A | AGTGTGTG others(1): Show |
4 | a0001c0001t0002g0202 a0002c0002t0001g0062 a0002c0002t0002g0061 others(1): Show |
4 | HG00735.hp1 HG01884.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+5668_525+5675d others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | ||||||
| chr2:85289221 | A | AGTGTGTG others(5): Show |
5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0208 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+5664_525+5675d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | ||||||
| chr2:85289221 | AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+5662_525+5675d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289221 | ||||||
| chr2:85289457 | G | T | 2 | a0001c0001t0002g0181 a0002c0002t0001g0109 |
2 | NA18959.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.525+5879G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289457 | |||||||
| chr2:85289667 | G | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.525+6089G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289667 | |||||||
| chr2:85289916 | C | T | 21 | a0001c0001t0001g0099 a0001c0001t0001g0112 a0001c0001t0001g0126 others(18): Show |
21 | HG00741.hp2 HG01106.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.525+6338C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289916 | |||||||
| chr2:85289918 | C | T | 1 | a0002c0009t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.525+6340C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289918 | |||||||
| chr2:85289965 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.525+6387C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289965 | |||||||
| chr2:85289967 | C | G | 78 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0088 others(75): Show |
78 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.525+6389C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85289967 | |||||||
| chr2:85289976 | G | GT | 14 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0002g0102 others(11): Show |
14 | HG01106.hp1 HG01168.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.525+6413dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289976 | ||||||
| chr2:85289976 | GT | G | 102 | a0001c0001t0001g0014 a0001c0001t0001g0076 a0001c0001t0001g0088 others(99): Show |
102 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.525+6413delT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85289976 | ||||||
| chr2:85290071 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0218 a0001c0001t0002g0125 others(4): Show |
7 | HG02080.hp1 HG02258.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+6493G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290071 | |||||||
| chr2:85290077 | A | G | 23 | a0001c0001t0001g0099 a0001c0001t0001g0112 a0001c0001t0001g0126 others(20): Show |
23 | HG00741.hp2 HG01106.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.525+6499A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290077 | |||||||
| chr2:85290169 | C | T | 89 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(86): Show |
89 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.525+6591C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290169 | |||||||
| chr2:85290263 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0111 a0001c0001t0001g0128 others(18): Show |
21 | HG01074.hp1 HG01106.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.525+6685G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290263 | |||||||
| chr2:85290372 | C | T | 3 | a0002c0002t0001g0069 a0002c0002t0001g0081 a0002c0002t0004g0085 |
3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.525+6794C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290372 | |||||||
| chr2:85290400 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.525+6822T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290400 | |||||||
| chr2:85290430 | T | A | 30 | a0001c0001t0001g0014 a0001c0001t0001g0111 a0001c0001t0001g0128 others(27): Show |
30 | HG01074.hp1 HG01106.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.525+6852T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290430 | |||||||
| chr2:85290467 | T | C | 68 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0096 others(65): Show |
68 | HG00597.hp2 HG00738.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.525+6889T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290467 | |||||||
| chr2:85290627 | A | G | 68 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0107 others(65): Show |
68 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.525+7049A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290627 | |||||||
| chr2:85290646 | G | A | 63 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0107 others(60): Show |
63 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.525+7068G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290646 | |||||||
| chr2:85290660 | A | G | 28 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0001g0161 others(25): Show |
28 | HG01074.hp2 HG01109.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.525+7082A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290660 | |||||||
| chr2:85290668 | C | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0179 others(8): Show |
11 | HG02129.hp2 HG02257.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+7090C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290668 | |||||||
| chr2:85290691 | T | G | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.525+7113T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290691 | |||||||
| chr2:85290706 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0011g0142 |
2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.525+7128C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290706 | |||||||
| chr2:85290783 | G | A | 14 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0170 others(11): Show |
14 | HG00738.hp2 HG01106.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.525+7205G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85290783 | |||||||
| chr2:85291042 | C | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.525+7464C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291042 | |||||||
| chr2:85291094 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0197 a0001c0001t0001g0208 others(3): Show |
6 | HG02257.hp2 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+7516T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291094 | |||||||
| chr2:85291141 | A | G | 1 | a0001c0001t0005g0001 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.525+7563A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291141 | |||||||
| chr2:85291151 | C | T | 4 | a0002c0002t0001g0034 a0002c0002t0001g0069 a0002c0002t0001g0081 others(1): Show |
4 | HG02895.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+7573C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291151 | |||||||
| chr2:85291360 | T | C | 25 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0111 others(22): Show |
25 | HG00280.hp2 HG01074.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.525+7782T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291360 | |||||||
| chr2:85291431 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.525+7853A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291431 | |||||||
| chr2:85291493 | C | T | 1 | a0002c0002t0002g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.525+7915C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291493 | |||||||
| chr2:85291560 | A | AGTTTTG | 2 | a0001c0001t0001g0183 a0002c0003t0002g0036 |
2 | HG02451.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.525+8012_525+8017d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291560 | ||||||
| chr2:85291560 | AGTTTTG | A | 64 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0090 others(61): Show |
64 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.525+8012_525+8017d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291560 | ||||||
| chr2:85291560 | AGTTTTGG others(5): Show |
A | 19 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0098 others(16): Show |
19 | HG00735.hp1 HG00735.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.525+8006_525+8017d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291560 | ||||||
| chr2:85291591 | G | T | 14 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0098 others(11): Show |
14 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.525+8013G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291591 | |||||||
| chr2:85291725 | T | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.525+8147T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291725 | |||||||
| chr2:85291954 | T | C | 15 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0098 others(12): Show |
15 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.525+8376T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85291954 | |||||||
| chr2:85291982 | TGGTCATA others(330): Show |
T | 210 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(207): Show |
210 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(207): Show |
intron_variant | MODIFIER | c.525+8421_525+8757d others(2): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291982 | ||||||
| chr2:85291993 | A | AT | 5 | a0001c0001t0001g0214 a0001c0001t0002g0166 a0002c0002t0001g0173 others(2): Show |
5 | HG00738.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+8460dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291993 | ||||||
| chr2:85291993 | A | ATTTTTT | 6 | a0001c0001t0002g0147 a0001c0001t0005g0002 a0002c0002t0001g0050 others(3): Show |
6 | HG01258.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+8455_525+8460d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85291993 | ||||||
| chr2:85292580 | C | T | 3 | a0001c0001t0005g0004 a0004c0005t0001g0135 a0004c0005t0009g0204 |
3 | HG01168.hp1 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.525+9002C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85292580 | |||||||
| chr2:85292717 | C | A | 6 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(3): Show |
6 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+9139C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85292717 | |||||||
| chr2:85293065 | C | T | 13 | a0001c0001t0001g0107 a0001c0001t0001g0139 a0001c0001t0001g0140 others(10): Show |
13 | HG01071.hp1 HG01261.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-9419C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293065 | |||||||
| chr2:85293149 | A | G | 3 | a0001c0001t0002g0162 a0001c0001t0002g0210 a0010c0011t0002g0231 |
3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.526-9335A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293149 | |||||||
| chr2:85293415 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.526-9069C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293415 | |||||||
| chr2:85293811 | A | G | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526-8673A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293811 | |||||||
| chr2:85293922 | C | T | 2 | a0001c0001t0002g0185 a0002c0002t0002g0011 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.526-8562C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293922 | |||||||
| chr2:85293965 | A | C | 40 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0230 others(37): Show |
40 | HG00280.hp2 HG01168.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.526-8519A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293965 | |||||||
| chr2:85293965 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.526-8519A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293965 | |||||||
| chr2:85293982 | C | A | 151 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(148): Show |
151 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.526-8502C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85293982 | |||||||
| chr2:85294026 | A | AT | 15 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0002g0116 others(12): Show |
15 | HG00738.hp1 HG01175.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.526-8430dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTT | 6 | a0001c0001t0002g0162 a0002c0002t0001g0069 a0002c0002t0008g0059 others(3): Show |
6 | HG02559.hp1 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-8435_526-8430d others(8): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT | 15 | a0001c0001t0001g0108 a0001c0001t0001g0124 a0001c0001t0001g0130 others(12): Show |
15 | HG01261.hp2 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.526-8436_526-8430d others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT others(1): Show |
29 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0091 others(26): Show |
29 | HG01074.hp1 HG01109.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.526-8437_526-8430d others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT others(2): Show |
36 | a0001c0001t0001g0088 a0001c0001t0001g0107 a0001c0001t0001g0122 others(33): Show |
36 | HG00639.hp2 HG01109.hp2 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.526-8438_526-8430d others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT others(3): Show |
12 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0001g0183 others(9): Show |
12 | HG01256.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.526-8439_526-8430d others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0090 a0001c0001t0001g0126 a0001c0001t0001g0209 others(1): Show |
4 | HG02135.hp2 HG03225.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-8440_526-8430d others(13): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0192 a0002c0002t0001g0064 |
2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.526-8442_526-8430d others(15): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT others(8): Show |
1 | a0002c0002t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.526-8444_526-8430d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294026 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0213 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.526-8447_526-8430d others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294026 | ||||||
| chr2:85294045 | T | TTTTTTTC | 14 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0001g0154 others(11): Show |
14 | HG00621.hp1 HG01257.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.526-8433_526-8432i others(9): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294045 | ||||||
| chr2:85294045 | T | TTTTTTTT others(1): Show |
43 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0092 others(40): Show |
43 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.526-8432_526-8431i others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294045 | ||||||
| chr2:85294045 | T | TTTTTTTT others(2): Show |
5 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0002c0002t0001g0038 others(2): Show |
5 | HG00738.hp2 HG01071.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-8431_526-8430i others(11): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85294045 | ||||||
| chr2:85294046 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.526-8438T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294046 | |||||||
| chr2:85294048 | T | C | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-8436T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294048 | |||||||
| chr2:85294071 | CTGTCGCC others(8): Show |
C | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-8412_526-8398d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294071 | |||||||
| chr2:85294073 | G | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(157): Show |
160 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.526-8411G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294073 | |||||||
| chr2:85294092 | A | G | 1 | a0002c0002t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.526-8392A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294092 | |||||||
| chr2:85294100 | G | A | 4 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0005g0002 others(1): Show |
4 | HG01074.hp2 HG01243.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-8384G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294100 | |||||||
| chr2:85294129 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.526-8355C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294129 | |||||||
| chr2:85294130 | G | A | 1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.526-8354G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294130 | |||||||
| chr2:85294132 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-8352A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294132 | |||||||
| chr2:85294142 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.526-8342T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294142 | |||||||
| chr2:85294145 | G | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-8339G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294145 | |||||||
| chr2:85294282 | C | T | 2 | a0001c0001t0002g0098 a0002c0002t0001g0045 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-8202C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294282 | |||||||
| chr2:85294316 | G | C | 2 | a0001c0016t0001g0203 a0004c0005t0001g0135 |
2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.526-8168G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294316 | |||||||
| chr2:85294340 | A | G | 2 | a0001c0001t0007g0134 a0002c0002t0007g0006 |
2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.526-8144A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294340 | |||||||
| chr2:85294400 | G | A | 155 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(152): Show |
155 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.526-8084G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294400 | |||||||
| chr2:85294400 | G | C | 5 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0111 others(2): Show |
5 | HG01074.hp1 HG01175.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-8084G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294400 | |||||||
| chr2:85294789 | T | C | 161 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(158): Show |
161 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.526-7695T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85294789 | |||||||
| chr2:85295040 | T | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-7444T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295040 | |||||||
| chr2:85295070 | C | G | 25 | a0001c0001t0001g0214 a0001c0001t0002g0103 a0001c0001t0002g0129 others(22): Show |
25 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.526-7414C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295070 | |||||||
| chr2:85295111 | C | A | 1 | a0002c0002t0003g0078 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.526-7373C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295111 | |||||||
| chr2:85295119 | A | G | 1 | a0005c0006t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.526-7365A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295119 | |||||||
| chr2:85295262 | C | T | 2 | a0001c0001t0002g0098 a0002c0002t0001g0045 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-7222C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295262 | |||||||
| chr2:85295387 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-7097A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295387 | |||||||
| chr2:85295495 | C | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0148 a0002c0002t0003g0071 |
3 | HG00639.hp2 HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.526-6989C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295495 | |||||||
| chr2:85295775 | C | CT | 26 | a0001c0001t0001g0076 a0001c0001t0001g0112 a0001c0001t0001g0170 others(23): Show |
26 | HG00741.hp1 HG01167.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.526-6687dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85295775 | ||||||
| chr2:85295775 | C | CTT | 133 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(130): Show |
133 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(130): Show |
intron_variant | MODIFIER | c.526-6688_526-6687d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85295775 | ||||||
| chr2:85295775 | C | CTTT | 30 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0113 others(27): Show |
30 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.526-6689_526-6687d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85295775 | ||||||
| chr2:85295803 | C | A | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6681C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295803 | |||||||
| chr2:85295885 | C | T | 2 | a0001c0001t0002g0098 a0002c0002t0001g0045 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-6599C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85295885 | |||||||
| chr2:85296041 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-6443A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296041 | |||||||
| chr2:85296097 | G | A | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6387G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296097 | |||||||
| chr2:85296153 | A | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(157): Show |
160 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.526-6331A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296153 | |||||||
| chr2:85296182 | A | G | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6302A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296182 | |||||||
| chr2:85296353 | G | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(157): Show |
160 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.526-6131G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296353 | |||||||
| chr2:85296418 | T | G | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-6066T>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296418 | |||||||
| chr2:85296558 | G | C | 2 | a0001c0001t0002g0098 a0002c0002t0001g0045 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.526-5926G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85296558 | |||||||
| chr2:85297246 | A | G | 12 | a0001c0001t0001g0107 a0001c0001t0001g0139 a0001c0001t0001g0140 others(9): Show |
12 | HG01071.hp1 HG01261.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-5238A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297246 | |||||||
| chr2:85297280 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.526-5204C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297280 | |||||||
| chr2:85297322 | G | A | 2 | a0001c0001t0002g0165 a0002c0002t0004g0072 |
2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.526-5162G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297322 | |||||||
| chr2:85297367 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-5117G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297367 | |||||||
| chr2:85297545 | G | T | 5 | a0001c0001t0001g0208 a0002c0002t0001g0007 a0002c0002t0001g0012 others(2): Show |
5 | HG02145.hp1 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-4939G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297545 | |||||||
| chr2:85297551 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526-4933C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297551 | |||||||
| chr2:85297635 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526-4849G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297635 | |||||||
| chr2:85297699 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-4785C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297699 | |||||||
| chr2:85297726 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-4758A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297726 | |||||||
| chr2:85297753 | C | T | 155 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(152): Show |
155 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.526-4731C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297753 | |||||||
| chr2:85297895 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.526-4589T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297895 | |||||||
| chr2:85297901 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.526-4583G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297901 | |||||||
| chr2:85297912 | C | T | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-4572C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297912 | |||||||
| chr2:85297996 | C | T | 6 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(3): Show |
6 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-4488C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85297996 | |||||||
| chr2:85298026 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.526-4458C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298026 | |||||||
| chr2:85298083 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.526-4401G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298083 | |||||||
| chr2:85298191 | C | CAAAA | 6 | a0001c0001t0001g0136 a0001c0001t0002g0116 a0001c0001t0002g0127 others(3): Show |
6 | HG01109.hp1 HG01168.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-4281_526-4278d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298191 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0156 |
2 | HG01074.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.526-4287_526-4278d others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298191 | C | CAAAAAAA others(4): Show |
44 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0096 others(41): Show |
44 | HG00639.hp2 HG01071.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.526-4288_526-4278d others(13): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298191 | C | CAAAAAAA others(5): Show |
49 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(46): Show |
49 | HG00621.hp2 HG01109.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.526-4289_526-4278d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298191 | C | CAAAAAAA others(6): Show |
77 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0092 others(74): Show |
77 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.526-4290_526-4278d others(15): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298191 | C | CAAAAAAA others(7): Show |
16 | a0001c0001t0001g0133 a0001c0001t0001g0141 a0001c0001t0001g0154 others(13): Show |
16 | HG01106.hp2 HG01934.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.526-4291_526-4278d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298191 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0002g0193 a0001c0001t0002g0202 a0003c0004t0002g0106 others(1): Show |
4 | HG00735.hp2 HG01884.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-4292_526-4278d others(17): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298191 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0002g0105 a0003c0004t0002g0114 a0009c0014t0002g0164 |
3 | HG02148.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.526-4278_526-4277i others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298191 | ||||||
| chr2:85298216 | G | A | 152 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(149): Show |
152 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.526-4268G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298216 | |||||||
| chr2:85298218 | G | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-4266G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298218 | |||||||
| chr2:85298221 | C | T | 4 | a0001c0001t0002g0098 a0001c0001t0007g0134 a0002c0002t0001g0045 others(1): Show |
4 | HG01256.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-4263C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298221 | |||||||
| chr2:85298223 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.526-4261G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298223 | |||||||
| chr2:85298350 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0229 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526-4134G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298350 | |||||||
| chr2:85298367 | C | T | 187 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(184): Show |
187 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.526-4117C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298367 | |||||||
| chr2:85298481 | C | CA | 22 | a0001c0001t0001g0088 a0001c0001t0001g0144 a0001c0001t0001g0156 others(19): Show |
22 | HG01168.hp2 HG01243.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-3982dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | ||||||
| chr2:85298481 | C | CAA | 20 | a0001c0001t0001g0136 a0001c0001t0002g0116 a0001c0001t0002g0127 others(17): Show |
20 | HG00280.hp2 HG01168.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.526-3983_526-3982d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | ||||||
| chr2:85298481 | C | CAAA | 6 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0002c0002t0001g0030 others(3): Show |
6 | HG01109.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-3984_526-3982d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | ||||||
| chr2:85298481 | CA | C | 59 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0092 others(56): Show |
59 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.526-3982delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85298481 | ||||||
| chr2:85298499 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.526-3985A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298499 | |||||||
| chr2:85298500 | AAAG | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(2): Show |
5 | HG00735.hp1 HG00735.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-3983_526-3981d others(5): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298500 | |||||||
| chr2:85298587 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-3897A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298587 | |||||||
| chr2:85298699 | GGC | G | 19 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0002g0116 others(16): Show |
19 | HG00280.hp2 HG01975.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.526-3784_526-3783d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298699 | |||||||
| chr2:85298875 | C | G | 1 | a0008c0015t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.526-3609C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298875 | |||||||
| chr2:85298907 | C | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0001g0226 others(2): Show |
5 | HG02135.hp1 NA18951.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-3577C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298907 | |||||||
| chr2:85298918 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.526-3566C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85298918 | |||||||
| chr2:85299111 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.526-3373A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299111 | |||||||
| chr2:85299276 | G | A | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.526-3208G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299276 | |||||||
| chr2:85299386 | CTA | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0218 a0001c0001t0006g0003 |
3 | HG01516.hp1 HG02258.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.526-3097_526-3096d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299386 | |||||||
| chr2:85299455 | G | A | 6 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(3): Show |
6 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-3029G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299455 | |||||||
| chr2:85299492 | CA | C | 48 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0090 others(45): Show |
48 | HG00621.hp2 HG01074.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.526-2991delA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299492 | |||||||
| chr2:85299576 | G | A | 1 | a0004c0005t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.526-2908G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299576 | |||||||
| chr2:85299683 | A | G | 22 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0002g0116 others(19): Show |
22 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-2801A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299683 | |||||||
| chr2:85299790 | T | C | 187 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(184): Show |
187 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.526-2694T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299790 | |||||||
| chr2:85299846 | G | A | 1 | a0005c0006t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.526-2638G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299846 | |||||||
| chr2:85299860 | A | AAC | 5 | a0001c0001t0002g0147 a0002c0002t0002g0027 a0002c0002t0002g0046 others(2): Show |
5 | HG00738.hp1 HG01168.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2581_526-2580d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACAC | 4 | a0001c0001t0001g0151 a0001c0001t0001g0214 a0003c0004t0002g0106 others(1): Show |
4 | HG00735.hp2 HG01109.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-2583_526-2580d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(1): Show |
5 | a0001c0001t0001g0112 a0002c0002t0002g0018 a0002c0002t0002g0066 others(2): Show |
5 | HG02723.hp1 HG03491.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-2587_526-2580d others(10): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(3): Show |
1 | a0002c0002t0001g0064 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.526-2589_526-2580d others(12): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(5): Show |
4 | a0001c0001t0001g0213 a0001c0001t0002g0102 a0002c0002t0001g0040 others(1): Show |
4 | HG01071.hp1 HG01346.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-2591_526-2580d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(7): Show |
8 | a0001c0001t0001g0160 a0001c0001t0001g0179 a0001c0001t0001g0211 others(5): Show |
8 | HG01256.hp1 HG01891.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.526-2593_526-2580d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(9): Show |
5 | a0001c0001t0001g0126 a0001c0001t0001g0192 a0002c0002t0001g0032 others(2): Show |
5 | HG01261.hp1 HG02135.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2595_526-2580d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(11): Show |
14 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0001g0130 others(11): Show |
14 | HG00621.hp1 HG00738.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.526-2597_526-2580d others(20): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(13): Show |
11 | a0001c0001t0001g0119 a0001c0001t0001g0128 a0001c0001t0001g0149 others(8): Show |
11 | HG00280.hp1 HG01257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.526-2599_526-2580d others(22): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(15): Show |
19 | a0001c0001t0001g0014 a0001c0001t0001g0090 a0001c0001t0001g0091 others(16): Show |
19 | HG00597.hp1 HG00597.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.526-2601_526-2580d others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(17): Show |
28 | a0001c0001t0001g0122 a0001c0001t0001g0138 a0001c0001t0001g0145 others(25): Show |
28 | HG00280.hp2 HG00741.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.526-2603_526-2580d others(26): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(19): Show |
24 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0001g0111 others(21): Show |
24 | HG00621.hp2 HG00639.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.526-2605_526-2580d others(28): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(21): Show |
11 | a0001c0001t0001g0092 a0001c0001t0001g0124 a0001c0001t0001g0153 others(8): Show |
11 | HG01175.hp1 HG01516.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-2607_526-2580d others(30): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(23): Show |
13 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0108 others(10): Show |
13 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-2609_526-2580d others(32): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(25): Show |
11 | a0001c0001t0001g0133 a0001c0001t0001g0152 a0001c0001t0001g0178 others(8): Show |
11 | HG01981.hp1 HG02056.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.526-2611_526-2580d others(34): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(27): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0226 a0001c0001t0002g0118 others(2): Show |
5 | HG06807.hp1 NA18906.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-2613_526-2580d others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(29): Show |
4 | a0001c0001t0001g0141 a0001c0001t0002g0175 a0002c0002t0001g0089 others(1): Show |
4 | HG01109.hp1 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.526-2615_526-2580d others(38): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(33): Show |
2 | a0001c0001t0001g0189 a0002c0002t0002g0058 |
2 | HG02717.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.526-2619_526-2580d others(42): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | AACACACA others(37): Show |
2 | a0002c0002t0001g0052 a0002c0002t0002g0017 |
2 | HG03017.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.526-2623_526-2580d others(46): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0031 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.526-2624_526-2623i others(19): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | |||||||
| chr2:85299860 | A | ACACACAC others(12): Show |
1 | a0001c0001t0002g0159 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.526-2624_526-2623i others(21): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | |||||||
| chr2:85299860 | A | ACACACAC others(14): Show |
1 | a0001c0001t0001g0099 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.526-2624_526-2623i others(23): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | |||||||
| chr2:85299860 | A | ACACACAC others(22): Show |
5 | a0001c0001t0001g0104 a0001c0001t0001g0224 a0001c0001t0002g0174 others(2): Show |
5 | HG02083.hp2 HG03139.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-2624_526-2623i others(31): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | |||||||
| chr2:85299860 | A | ACACACAC others(26): Show |
2 | a0001c0001t0001g0144 a0001c0001t0002g0110 |
2 | NA18967.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.526-2624_526-2623i others(35): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | |||||||
| chr2:85299860 | A | ACACACAC others(28): Show |
1 | a0001c0001t0002g0167 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.526-2624_526-2623i others(37): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299860 | |||||||
| chr2:85299860 | AAC | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(2): Show |
5 | HG01106.hp1 HG01358.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2581_526-2580d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | AACAC | A | 3 | a0001c0001t0002g0193 a0001c0001t0002g0202 a0009c0014t0002g0164 |
3 | HG01884.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.526-2583_526-2580d others(6): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | AACACACA others(5): Show |
A | 1 | a0004c0005t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.526-2591_526-2580d others(14): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | AACACACA others(7): Show |
A | 5 | a0001c0016t0001g0203 a0002c0002t0002g0043 a0002c0002t0004g0085 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-2593_526-2580d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299860 | AACACACA others(9): Show |
A | 13 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0002g0067 others(10): Show |
13 | HG01168.hp1 HG01261.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-2595_526-2580d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85299860 | ||||||
| chr2:85299949 | C | T | 1 | a0007c0013t0001g0143 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.526-2535C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299949 | |||||||
| chr2:85299955 | G | A | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-2529G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299955 | |||||||
| chr2:85299973 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.526-2511C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85299973 | |||||||
| chr2:85300166 | A | G | 6 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0196 others(3): Show |
6 | HG01167.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.526-2318A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300166 | |||||||
| chr2:85300261 | T | C | 1 | a0002c0003t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.526-2223T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300261 | |||||||
| chr2:85300328 | T | C | 23 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0002g0116 others(20): Show |
23 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.526-2156T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300328 | |||||||
| chr2:85300434 | A | T | 22 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0002g0116 others(19): Show |
22 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-2050A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300434 | |||||||
| chr2:85300463 | G | T | 32 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0212 others(29): Show |
32 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.526-2021G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300463 | |||||||
| chr2:85300578 | C | T | 23 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0002g0116 others(20): Show |
23 | HG00280.hp2 HG01243.hp1 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.526-1906C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300578 | |||||||
| chr2:85300649 | G | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0218 a0001c0001t0006g0003 |
3 | HG01516.hp1 HG02258.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.526-1835G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300649 | |||||||
| chr2:85300738 | G | T | 12 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0002g0067 others(9): Show |
12 | HG01261.hp2 HG02258.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-1746G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300738 | |||||||
| chr2:85300783 | C | CT | 13 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(10): Show |
13 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.526-1687dupT | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85300783 | ||||||
| chr2:85300851 | C | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1633C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300851 | |||||||
| chr2:85300946 | A | C | 1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.526-1538A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300946 | |||||||
| chr2:85300999 | C | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0198 |
2 | HG02080.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.526-1485C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85300999 | |||||||
| chr2:85301086 | C | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1398C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301086 | |||||||
| chr2:85301123 | ACTTAT | A | 4 | a0001c0001t0002g0098 a0001c0001t0007g0134 a0002c0002t0001g0045 others(1): Show |
4 | HG01256.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-1355_526-1351d others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85301123 | ||||||
| chr2:85301128 | T | C | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1356T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301128 | |||||||
| chr2:85301132 | A | T | 1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-1352A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301132 | |||||||
| chr2:85301146 | T | C | 10 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-1338T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301146 | |||||||
| chr2:85301172 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.526-1312A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301172 | |||||||
| chr2:85301184 | T | A | 1 | a0002c0002t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.526-1300T>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301184 | |||||||
| chr2:85301261 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-1223G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301261 | |||||||
| chr2:85301520 | A | G | 10 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-964A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301520 | |||||||
| chr2:85301572 | T | TTTTC | 10 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-910_526-907dup others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85301572 | ||||||
| chr2:85301681 | A | C | 1 | a0006c0017t0001g0215 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.526-803A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301681 | |||||||
| chr2:85301719 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.526-765G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301719 | |||||||
| chr2:85301784 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.526-700A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301784 | |||||||
| chr2:85301861 | C | T | 1 | a0001c0001t0007g0134 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.526-623C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301861 | |||||||
| chr2:85301896 | C | T | 1 | a0001c0001t0006g0005 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.526-588C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301896 | |||||||
| chr2:85301897 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.526-587G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301897 | |||||||
| chr2:85301967 | A | C | 2 | a0002c0002t0001g0009 a0002c0002t0001g0087 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.526-517A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | chr2 | 85301967 | |||||||
| chr2:85302144 | C | CA | 9 | a0001c0001t0001g0111 a0001c0001t0001g0151 a0001c0001t0001g0155 others(6): Show |
9 | HG01074.hp1 HG01109.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-330dupA | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 85302144 | ||||||
| chr2:85302658 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.658+42C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302658 | |||||||
| chr2:85302717 | C | T | 2 | a0001c0001t0002g0185 a0002c0002t0002g0011 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.658+101C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302717 | |||||||
| chr2:85302858 | A | G | 156 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(153): Show |
156 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.658+242A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302858 | |||||||
| chr2:85302904 | T | C | 22 | a0001c0001t0001g0212 a0001c0001t0001g0230 a0001c0001t0002g0116 others(19): Show |
22 | HG00280.hp2 HG01243.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.658+288T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302904 | |||||||
| chr2:85302942 | T | C | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.658+326T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302942 | |||||||
| chr2:85302943 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.658+327G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302943 | |||||||
| chr2:85302994 | C | G | 1 | a0002c0002t0002g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.658+378C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85302994 | |||||||
| chr2:85303270 | C | G | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.659-625C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303270 | |||||||
| chr2:85303276 | G | A | 30 | a0001c0001t0001g0088 a0001c0001t0001g0161 a0001c0001t0001g0163 others(27): Show |
30 | HG00735.hp1 HG00735.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.659-619G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303276 | |||||||
| chr2:85303295 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.659-600G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303295 | |||||||
| chr2:85303304 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.659-591G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303304 | |||||||
| chr2:85303438 | A | G | 209 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(206): Show |
209 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.659-457A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303438 | |||||||
| chr2:85303540 | G | A | 3 | a0001c0001t0002g0162 a0001c0001t0002g0210 a0010c0011t0002g0231 |
3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.659-355G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303540 | |||||||
| chr2:85303553 | T | C | 10 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.659-342T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303553 | |||||||
| chr2:85303673 | G | A | 1 | a0002c0002t0001g0056 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.659-222G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 5/11 | chr2 | 85303673 | |||||||
| chr2:85304128 | A | G | 15 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0002g0067 others(12): Show |
15 | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.762-127A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 6/11 | chr2 | 85304128 | |||||||
| chr2:85304373 | T | C | 2 | a0002c0002t0001g0109 a0002c0002t0003g0080 |
2 | HG02132.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.845+35T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304373 | |||||||
| chr2:85304445 | C | G | 2 | a0002c0002t0002g0018 a0002c0002t0002g0066 |
2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.845+107C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304445 | |||||||
| chr2:85304456 | C | A | 73 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0092 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.845+118C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304456 | |||||||
| chr2:85304667 | T | C | 6 | a0001c0001t0002g0129 a0001c0001t0002g0132 a0001c0001t0002g0166 others(3): Show |
6 | HG01074.hp2 HG01243.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.845+329T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304667 | |||||||
| chr2:85304684 | C | A | 212 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(209): Show |
212 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(209): Show |
intron_variant | MODIFIER | c.845+346C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304684 | |||||||
| chr2:85304795 | T | C | 16 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0002g0067 others(13): Show |
16 | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.845+457T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304795 | |||||||
| chr2:85304803 | G | A | 2 | a0001c0001t0007g0134 a0002c0002t0007g0006 |
2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.846-457G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304803 | |||||||
| chr2:85304808 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.846-452G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304808 | |||||||
| chr2:85304988 | C | T | 2 | a0001c0001t0007g0134 a0002c0002t0007g0006 |
2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.846-272C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304988 | |||||||
| chr2:85304999 | C | A | 3 | a0001c0001t0002g0162 a0001c0001t0002g0210 a0010c0011t0002g0231 |
3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.846-261C>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85304999 | |||||||
| chr2:85305082 | C | G | 213 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(210): Show |
213 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.846-178C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85305082 | |||||||
| chr2:85305147 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.846-113T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 7/11 | chr2 | 85305147 | |||||||
| chr2:85305457 | G | A | 1 | a0003c0004t0002g0114 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.989+54G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305457 | |||||||
| chr2:85305462 | C | G | 4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0223 others(1): Show |
4 | HG01346.hp1 HG01891.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.989+59C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305462 | |||||||
| chr2:85305478 | A | C | 1 | a0005c0006t0002g0137 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.989+75A>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305478 | |||||||
| chr2:85305689 | G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.989+286G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305689 | |||||||
| chr2:85305745 | G | C | 2 | a0001c0001t0002g0098 a0002c0002t0008g0059 |
2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.989+342G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305745 | |||||||
| chr2:85305862 | C | T | 1 | a0002c0002t0004g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.990-344C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305862 | |||||||
| chr2:85305909 | C | T | 1 | a0002c0002t0003g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.990-297C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85305909 | |||||||
| chr2:85306039 | G | A | 1 | a0005c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.990-167G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85306039 | |||||||
| chr2:85306104 | G | A | 18 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0140 others(15): Show |
18 | HG01071.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.990-102G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 8/11 | chr2 | 85306104 | |||||||
| chr2:85306448 | C | G | 18 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0002g0067 others(15): Show |
18 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.1150-4C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 9/11 | chr2 | 85306448 | |||||||
| chr2:85306719 | C | T | 13 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0002g0067 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1257+160C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306719 | |||||||
| chr2:85306734 | G | A | 5 | a0001c0001t0002g0185 a0002c0002t0002g0011 a0002c0002t0002g0016 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+175G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306734 | |||||||
| chr2:85306864 | CTG | C | 2 | a0002c0002t0001g0009 a0002c0002t0001g0087 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1257+309_1257+310d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 85306864 | ||||||
| chr2:85306881 | G | T | 5 | a0001c0001t0002g0193 a0001c0001t0002g0202 a0002c0002t0004g0085 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257+322G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306881 | |||||||
| chr2:85306900 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0002g0125 |
2 | NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1257+341G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306900 | |||||||
| chr2:85306916 | G | A | 21 | a0001c0001t0001g0099 a0001c0001t0001g0145 a0001c0001t0001g0212 others(18): Show |
21 | HG00280.hp2 HG01167.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1257+357G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85306916 | |||||||
| chr2:85307080 | G | T | 15 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(12): Show |
15 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1257+521G>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307080 | |||||||
| chr2:85307119 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1258-523A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307119 | |||||||
| chr2:85307173 | T | TAACCC | 148 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(145): Show |
148 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.1258-467_1258-463d others(7): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 85307173 | ||||||
| chr2:85307192 | C | T | 5 | a0001c0001t0002g0067 a0001c0001t0002g0157 a0001c0001t0005g0001 others(2): Show |
5 | HG01261.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258-450C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307192 | |||||||
| chr2:85307214 | G | A | 3 | a0001c0016t0001g0203 a0004c0005t0001g0135 a0004c0005t0009g0204 |
3 | HG02615.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1258-428G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307214 | |||||||
| chr2:85307243 | A | G | 8 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(5): Show |
8 | HG00735.hp1 HG00735.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1258-399A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307243 | |||||||
| chr2:85307269 | T | C | 44 | a0001c0001t0001g0088 a0001c0001t0001g0161 a0001c0001t0001g0163 others(41): Show |
44 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-373T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307269 | |||||||
| chr2:85307390 | G | C | 1 | a0002c0002t0001g0169 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1258-252G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307390 | |||||||
| chr2:85307406 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1258-236T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307406 | |||||||
| chr2:85307444 | G | A | 9 | a0001c0001t0002g0125 a0001c0001t0002g0147 a0001c0001t0002g0165 others(6): Show |
9 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1258-198G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307444 | |||||||
| chr2:85307446 | G | A | 28 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(25): Show |
28 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1258-196G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307446 | |||||||
| chr2:85307451 | T | C | 44 | a0001c0001t0001g0088 a0001c0001t0001g0161 a0001c0001t0001g0163 others(41): Show |
44 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1258-191T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307451 | |||||||
| chr2:85307574 | C | T | 3 | a0001c0001t0002g0162 a0001c0001t0002g0210 a0010c0011t0002g0231 |
3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1258-68C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 10/11 | chr2 | 85307574 | |||||||
| chr2:85307820 | G | A | 3 | a0001c0001t0002g0162 a0001c0001t0002g0210 a0010c0011t0002g0231 |
3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1333+103G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85307820 | |||||||
| chr2:85307827 | G | A | 21 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0002g0105 others(18): Show |
21 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1333+110G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85307827 | |||||||
| chr2:85307887 | G | C | 1 | a0002c0002t0001g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1333+170G>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85307887 | |||||||
| chr2:85308064 | C | T | 11 | a0001c0001t0002g0125 a0001c0001t0002g0147 a0001c0001t0002g0165 others(8): Show |
11 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1333+347C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308064 | |||||||
| chr2:85308099 | C | T | 3 | a0001c0001t0002g0193 a0001c0001t0002g0202 a0009c0014t0002g0164 |
3 | HG01884.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1333+382C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308099 | |||||||
| chr2:85308163 | GCA | G | 2 | a0001c0001t0007g0134 a0002c0002t0007g0006 |
2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1333+448_1333+449d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308163 | ||||||
| chr2:85308178 | A | T | 7 | a0001c0001t0001g0149 a0001c0001t0001g0208 a0002c0002t0001g0007 others(4): Show |
7 | HG02145.hp1 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1333+461A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308178 | |||||||
| chr2:85308180 | C | T | 1 | a0005c0006t0010g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1333+463C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308180 | |||||||
| chr2:85308181 | A | G | 39 | a0001c0001t0001g0088 a0001c0001t0001g0161 a0001c0001t0001g0163 others(36): Show |
39 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1333+464A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308181 | |||||||
| chr2:85308197 | T | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0001c0001t0002g0193 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1333+480T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308197 | |||||||
| chr2:85308246 | T | C | 7 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 others(4): Show |
7 | HG01257.hp2 HG01934.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1333+529T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308246 | |||||||
| chr2:85308290 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1333+573A>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308290 | |||||||
| chr2:85308314 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1333+597C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308314 | |||||||
| chr2:85308376 | C | CCATTCTC others(101): Show |
1 | a0002c0002t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1334-652_1334-651i others(110): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308376 | ||||||
| chr2:85308376 | C | CCATTCTC others(81): Show |
10 | a0001c0001t0002g0125 a0001c0001t0002g0147 a0001c0001t0002g0165 others(7): Show |
10 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1334-652_1334-651i others(90): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308376 | ||||||
| chr2:85308382 | A | ACCTTCCC others(29): Show |
1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(38): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | ||||||
| chr2:85308382 | A | ACCTTCCC others(76): Show |
58 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0091 others(55): Show |
58 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(85): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | ||||||
| chr2:85308382 | A | ACCTTCCC others(96): Show |
3 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0002c0002t0004g0085 |
3 | HG01109.hp2 NA18522.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(105): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | ||||||
| chr2:85308382 | A | ACCTTCCC others(317): Show |
1 | a0002c0002t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(326): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | ||||||
| chr2:85308382 | A | ACCTTCCC others(77): Show |
2 | a0002c0002t0001g0022 a0002c0002t0001g0023 |
2 | HG02735.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1334-587_1334-586i others(86): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308382 | ||||||
| chr2:85308382 | A | T | 13 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0002g0125 others(10): Show |
13 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1334-647A>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308382 | |||||||
| chr2:85308385 | T | TTCCCTCC others(108): Show |
2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(117): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(341): Show |
2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(350): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(81): Show |
1 | a0002c0003t0002g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(90): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(61): Show |
5 | a0001c0001t0002g0067 a0001c0001t0002g0157 a0001c0001t0005g0001 others(2): Show |
5 | HG01261.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(70): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(133): Show |
1 | a0002c0003t0002g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(142): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(77): Show |
28 | a0001c0001t0001g0099 a0001c0001t0001g0145 a0001c0001t0001g0177 others(25): Show |
28 | HG00280.hp2 HG01074.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(86): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(175): Show |
3 | a0001c0001t0001g0088 a0001c0001t0001g0201 a0002c0009t0001g0019 |
3 | HG02886.hp2 HG02895.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(184): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(357): Show |
2 | a0002c0002t0001g0069 a0002c0002t0001g0081 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(366): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308385 | T | TTCCCTCC others(57): Show |
7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0002g0196 others(4): Show |
7 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334-613_1334-612i others(66): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308385 | ||||||
| chr2:85308401 | T | TTCCCTCC others(68): Show |
1 | a0004c0005t0009g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1334-613_1334-612i others(77): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308401 | ||||||
| chr2:85308401 | T | TTCCCTCC others(73): Show |
1 | a0001c0001t0002g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(82): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308401 | ||||||
| chr2:85308409 | C | CTTTCCCC others(73): Show |
2 | a0001c0001t0002g0185 a0005c0006t0010g0233 |
2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(82): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308409 | ||||||
| chr2:85308409 | C | CTTTCCCC others(73): Show |
3 | a0001c0001t0002g0110 a0001c0001t0002g0118 a0004c0012t0002g0184 |
3 | NA18951.hp1 NA19011.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(82): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308409 | ||||||
| chr2:85308414 | C | CCCCTCCC others(163): Show |
2 | a0001c0001t0002g0193 a0009c0014t0002g0164 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1334-613_1334-612i others(172): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308414 | ||||||
| chr2:85308414 | C | CCCCTCCC others(309): Show |
1 | a0001c0001t0002g0202 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1334-613_1334-612i others(318): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308414 | ||||||
| chr2:85308417 | T | C | 133 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0091 others(130): Show |
133 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.1334-612T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308417 | |||||||
| chr2:85308417 | T | TTCCCTCC others(96): Show |
1 | a0008c0015t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1334-601_1334-600i others(105): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308417 | ||||||
| chr2:85308417 | T | TTCCCTCC others(161): Show |
1 | a0001c0001t0002g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1334-587_1334-586i others(170): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308417 | ||||||
| chr2:85308417 | T | TTCCCTCC others(33): Show |
7 | a0001c0001t0001g0230 a0002c0002t0001g0009 a0002c0002t0001g0030 others(4): Show |
7 | HG02109.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334-586_1334-585i others(42): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308417 | ||||||
| chr2:85308433 | C | CTCCCTCC others(9): Show |
1 | a0001c0001t0005g0004 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1334-586_1334-571d others(18): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308433 | ||||||
| chr2:85308442 | TTTCTCTT others(7): Show |
T | 1 | a0002c0002t0002g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1334-586_1334-573d others(16): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308442 | |||||||
| chr2:85308444 | T | C | 2 | a0001c0016t0001g0203 a0004c0005t0001g0135 |
2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1334-585T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308444 | |||||||
| chr2:85308447 | C | G | 141 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0088 others(138): Show |
141 | HG00280.hp2 HG00621.hp2 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.1334-582C>G | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308447 | |||||||
| chr2:85308447 | C | T | 2 | a0001c0016t0001g0203 a0004c0005t0001g0135 |
2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1334-582C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308447 | |||||||
| chr2:85308449 | T | C | 2 | a0001c0016t0001g0203 a0004c0005t0001g0135 |
2 | HG02615.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1334-580T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308449 | |||||||
| chr2:85308456 | CCT | C | 92 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0090 others(89): Show |
92 | HG00621.hp2 HG00639.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.1334-568_1334-567d others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308456 | ||||||
| chr2:85308457 | C | CTCCCTCC others(161): Show |
1 | a0004c0005t0001g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1334-570_1334-569i others(170): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | ||||||
| chr2:85308457 | C | CTCCCTCC others(15): Show |
1 | a0001c0016t0001g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1334-570_1334-569i others(24): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | ||||||
| chr2:85308457 | C | CTT | 14 | a0001c0001t0001g0230 a0001c0001t0002g0185 a0002c0002t0001g0009 others(11): Show |
14 | HG02109.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1334-571_1334-570i others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | ||||||
| chr2:85308457 | C | CTTTCTCT others(27): Show |
1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1334-571_1334-570i others(36): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308457 | ||||||
| chr2:85308483 | T | C | 11 | a0001c0001t0001g0090 a0001c0001t0001g0149 a0001c0001t0001g0190 others(8): Show |
11 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1334-546T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308483 | |||||||
| chr2:85308491 | C | T | 11 | a0001c0001t0001g0090 a0001c0001t0001g0149 a0001c0001t0001g0190 others(8): Show |
11 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1334-538C>T | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308491 | |||||||
| chr2:85308493 | TC | T | 25 | a0001c0001t0001g0088 a0001c0001t0001g0179 a0001c0001t0001g0192 others(22): Show |
25 | HG00639.hp1 HG00741.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1334-529delC | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85308493 | ||||||
| chr2:85308793 | G | A | 1 | a0002c0002t0008g0059 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1334-236G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308793 | |||||||
| chr2:85308903 | G | A | 2 | a0001c0001t0001g0131 a0002c0002t0003g0075 |
2 | HG00597.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1334-126G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308903 | |||||||
| chr2:85308919 | G | A | 2 | a0002c0002t0008g0059 a0004c0005t0009g0204 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1334-110G>A | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308919 | |||||||
| chr2:85308982 | T | C | 5 | a0001c0001t0002g0098 a0001c0001t0002g0110 a0001c0001t0002g0118 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1334-47T>C | TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | chr2 | 85308982 | |||||||
| chr2:85309005 | CTCTT | C | 2 | a0001c0001t0007g0134 a0002c0002t0007g0006 |
2 | HG01256.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1334-19_1334-16del others(4): Show |
TCF7L1 | ENSG00000152284.5 | transcript | ENST00000282111.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 85309005 |