Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81567 |
| ensemblid | ENSG00000239264.9 |
| hgncid | 21073 |
| symbol | TXNDC5 |
| name | thioredoxin domain containing 5 |
| refseq_nuc | NM_030810.5 |
| refseq_prot | NP_110437.2 |
| ensembl_nuc | ENST00000379757.9 |
| ensembl_prot | ENSP00000369081.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 7881517 |
| end | 7910788 |
| strand | - |
| ver | v1.2 |
| region | chr6:7881517-7910788 |
| region5000 | chr6:7876517-7915788 |
| regionname0 | TXNDC5_chr6_7881517_7910788 |
| regionname5000 | TXNDC5_chr6_7876517_7915788 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 432 | 388 | 94 | 65 | 170 | 16 | 41 | 128 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0002 | 0/0 | 433 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(428): Show |
chr6 | 7876517 | 7915788 |
| a0003 | 0/0 | 432 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0004 | 0/0 | 432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0005 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0006 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0007 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0008 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0009 | 0/0 | 432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| a0010 | 0/0 | 432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | MPARP others(427): Show |
chr6 | 7876517 | 7915788 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1296 | 329 | 68 | 55 | 150 | 14 | 40 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0001c0002 | 0/0 | 1296 | 27 | 22 | 2 | 0 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0001c0003 | 0/0 | 1296 | 24 | 0 | 7 | 17 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0001c0004 | 0/0 | 1296 | 5 | 4 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0001c0009 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0001c0010 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0001c0016 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0002c0005 | 0/0 | 1299 | 4 | 0 | 4 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1294): Show |
chr6 | 7876517 | 7915788 | ||
| a0003c0007 | 0/0 | 1296 | 2 | 0 | 1 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0004c0006 | 0/0 | 1296 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0005c0012 | 0/0 | 1296 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0006c0011 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0007c0013 | 0/0 | 1296 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0008c0008 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0009c0015 | 0/0 | 1296 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 | ||
| a0010c0014 | 0/0 | 1296 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | ATGCC others(1291): Show |
chr6 | 7876517 | 7915788 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2938 | 251 | 36 | 46 | 124 | 12 | 31 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0002 | 0/0 | 2923 | 15 | 14 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0003 | 0/0 | 2923 | 31 | 4 | 5 | 13 | 2 | 7 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0004 | 0/0 | 2923 | 7 | 7 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0005 | 0/0 | 2939 | 6 | 0 | 0 | 6 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2934): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0006 | 0/0 | 2938 | 4 | 1 | 1 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0008 | 0/0 | 2938 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0009 | 0/0 | 2933 | 2 | 1 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2928): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0011 | 0/0 | 2923 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0012 | 0/0 | 2923 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0013 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0014 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0015 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2956): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0016 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0018 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0019 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0020 | 0/0 | 2918 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2913): Show |
chr6 | 7876517 | 7915788 |
| a0001c0001t0022 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0002t0001 | 0/0 | 2938 | 5 | 5 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0002t0002 | 0/0 | 2923 | 15 | 10 | 2 | 0 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0001c0002t0007 | 0/0 | 2938 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0002t0010 | 0/0 | 2938 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0002t0021 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0003t0001 | 0/0 | 2938 | 24 | 0 | 7 | 17 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0004t0002 | 0/0 | 2923 | 5 | 4 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0001c0009t0001 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0010t0001 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0001c0016t0003 | 0/0 | 2923 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0002c0005t0001 | 0/0 | 2941 | 4 | 0 | 4 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2936): Show |
chr6 | 7876517 | 7915788 |
| a0003c0007t0001 | 0/0 | 2938 | 2 | 0 | 1 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0004c0006t0001 | 0/0 | 2938 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0005c0012t0001 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0006c0011t0002 | 0/0 | 2923 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0007c0013t0001 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0008c0008t0002 | 0/0 | 2923 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2918): Show |
chr6 | 7876517 | 7915788 |
| a0009c0015t0017 | 0/0 | 2938 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| a0010c0014t0001 | 0/0 | 2938 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | AGCCC others(2933): Show |
chr6 | 7876517 | 7915788 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 1 | 8 | 10 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0009 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0017 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0055 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0004g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0005g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0008g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0012g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0014g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0015g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0016g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0018g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0019g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0020g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0001t0022g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0007g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0010g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0002t0021g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0004t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0004t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0009t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0001c0016t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0002c0005t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0002c0005t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0003c0007t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0003c0007t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0004c0006t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0005c0012t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0006c0011t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0007c0013t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0008c0008t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0009c0015t0017g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| a0010c0014t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0241 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00621 | hp2 | a0001 | c0016 | t0003 | g0236 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0212 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00735 | hp1 | a0002 | c0005 | t0001 | g0022 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00741 | hp1 | a0001 | c0001 | t0016 | g0106 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG00741 | hp2 | a0005 | c0012 | t0001 | g0074 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0081 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01074 | hp2 | a0002 | c0005 | t0001 | g0022 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0124 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01261 | hp1 | a0002 | c0005 | t0001 | g0022 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01361 | hp1 | a0001 | c0004 | t0002 | g0123 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01433 | hp2 | a0002 | c0005 | t0001 | g0252 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0031 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0031 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0230 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01943 | hp1 | a0003 | c0007 | t0001 | g0250 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0159 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02165 | hp1 | a0001 | c0001 | t0020 | g0215 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02257 | hp1 | a0001 | c0002 | t0010 | g0118 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02258 | hp1 | a0006 | c0011 | t0002 | g0059 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0043 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02273 | hp2 | a0007 | c0013 | t0001 | g0154 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02280 | hp2 | a0001 | c0002 | t0010 | g0183 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0176 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0259 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0257 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02647 | hp1 | a0001 | c0002 | t0007 | g0119 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02723 | hp2 | a0001 | c0001 | t0015 | g0194 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0146 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02818 | hp2 | a0008 | c0008 | t0002 | g0056 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02896 | hp1 | a0004 | c0006 | t0001 | g0040 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02897 | hp1 | a0004 | c0006 | t0001 | g0040 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03041 | hp1 | a0001 | c0002 | t0007 | g0019 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0019 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0019 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03225 | hp1 | a0001 | c0002 | t0021 | g0253 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0131 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0073 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0216 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03654 | hp1 | a0009 | c0015 | t0017 | g0079 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0117 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03831 | hp2 | a0003 | c0007 | t0001 | g0251 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0217 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03942 | hp2 | a0010 | c0014 | t0001 | g0071 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18522 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18952 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18972 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18972 | hp2 | a0001 | c0009 | t0001 | g0057 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18981 | hp1 | a0001 | c0010 | t0001 | g0058 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19074 | hp1 | a0001 | c0001 | t0018 | g0144 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19076 | hp1 | a0001 | c0001 | t0022 | g0260 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19083 | hp1 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19083 | hp2 | a0001 | c0001 | t0012 | g0231 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA19240 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ASW | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0156 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02486 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0108 | REF | REF | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7883187 | G | A | 1 | a0007 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.1256C>T | p.Ser419Leu | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1268/2938 | 1256/1299 | 419/432 | chr6 | 7883187 | |||
| chr6:7884463 | G | A | 1 | a0010 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1072C>T | p.Pro358Ser | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/10 | 1084/2938 | 1072/1299 | 358/432 | chr6 | 7884463 | |||
| chr6:7885974 | A | G | 1 | a0004 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1033T>C | p.Phe345Leu | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/10 | 1045/2938 | 1033/1299 | 345/432 | chr6 | 7885974 | |||
| chr6:7889521 | G | C | 1 | a0009 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.793C>G | p.Leu265Val | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/10 | 805/2938 | 793/1299 | 265/432 | chr6 | 7889521 | |||
| chr6:7891641 | C | T | 1 | a0005 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.712G>A | p.Glu238Lys | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/10 | 724/2938 | 712/1299 | 238/432 | chr6 | 7891641 | |||
| chr6:7895115 | C | T | 1 | a0006 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.607G>A | p.Val203Ile | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/10 | 619/2938 | 607/1299 | 203/432 | chr6 | 7895115 | |||
| chr6:7910598 | G | A | 1 | a0008 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.179C>T | p.Pro60Leu | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 191/2938 | 179/1299 | 60/432 | chr6 | 7910598 | |||
| chr6:7910632 | G | A | 1 | a0003 | 2 | HG01943.hp1 HG03831.hp2 |
missense_variant | MODERATE | c.145C>T | p.Pro49Ser | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 157/2938 | 145/1299 | 49/432 | chr6 | 7910632 | |||
| chr6:7910637 | T | TCCG | 1 | a0002 | 4 | HG00735.hp1 HG01074.hp2 HG01261.hp1 others(1): Show |
conservative_inframe_insertion | MODERATE | c.137_139dupCGG | p.Ala46dup | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 151/2938 | 139/1299 | 47/432 | chr6 | 7910637 | |||
| chr6:7910745 | A | G | 1 | a0008 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.32T>C | p.Leu11Pro | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 44/2938 | 32/1299 | 11/432 | chr6 | 7910745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7883153 | G | A | 3 | a0001c0002 a0001c0004 a0006c0011 |
33 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(30): Show |
synonymous_variant | LOW | c.1290C>T | p.Asp430Asp | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1302/2938 | 1290/1299 | 430/432 | chr6 | 7883153 | |||
| chr6:7884419 | C | T | 1 | a0001c0003 | 24 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(21): Show |
synonymous_variant | LOW | c.1116G>A | p.Ala372Ala | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/10 | 1128/2938 | 1116/1299 | 372/432 | chr6 | 7884419 | |||
| chr6:7891714 | G | A | 1 | a0001c0004 | 5 | HG01361.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
synonymous_variant | LOW | c.639C>T | p.Phe213Phe | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/10 | 651/2938 | 639/1299 | 213/432 | chr6 | 7891714 | |||
| chr6:7904600 | G | A | 1 | a0001c0016 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.387C>T | p.Ser129Ser | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/10 | 399/2938 | 387/1299 | 129/432 | chr6 | 7904600 | |||
| chr6:7910681 | C | T | 1 | a0001c0010 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.96G>A | p.Gly32Gly | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 108/2938 | 96/1299 | 32/432 | chr6 | 7910681 | |||
| chr6:7910729 | C | T | 1 | a0001c0009 | 1 | NA18972.hp2 | synonymous_variant | LOW | c.48G>A | p.Ala16Ala | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 60/2938 | 48/1299 | 16/432 | chr6 | 7910729 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7881520 | T | A | 1 | a0001c0001t0016 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1624A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1624 | chr6 | 7881520 | ||||||
| chr6:7881520 | T | TA | 1 | a0001c0001t0005 | 6 | HG00609.hp2 HG02080.hp1 NA18954.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1623dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1623 | chr6 | 7881520 | ||||||
| chr6:7881521 | A | T | 1 | a0001c0001t0006 | 4 | HG01074.hp1 HG03490.hp1 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1623T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1623 | chr6 | 7881521 | ||||||
| chr6:7881563 | A | C | 1 | a0001c0001t0012 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1581T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1581 | chr6 | 7881563 | ||||||
| chr6:7881619 | GTTGTGTG others(4): Show |
G | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1514_*1524delTGTA others(7): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1514 | chr6 | 7881619 | ||||||
| chr6:7881631 | A | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1513T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1513 | chr6 | 7881631 | ||||||
| chr6:7881632 | G | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1512C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1512 | chr6 | 7881632 | ||||||
| chr6:7881698 | T | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1446A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1446 | chr6 | 7881698 | ||||||
| chr6:7881788 | G | C | 2 | a0001c0002t0007 a0001c0002t0021 |
5 | HG02647.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1356C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1356 | chr6 | 7881788 | ||||||
| chr6:7881843 | G | A | 1 | a0009c0015t0017 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1301C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1301 | chr6 | 7881843 | ||||||
| chr6:7881919 | CCTAT | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1221_*1224delATAG | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1221 | chr6 | 7881919 | ||||||
| chr6:7881972 | G | A | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1172C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1172 | chr6 | 7881972 | ||||||
| chr6:7882046 | C | CCAGAGCA others(16): Show |
1 | a0001c0001t0015 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075_*1097dupACAG others(19): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1097 | chr6 | 7882046 | ||||||
| chr6:7882100 | C | T | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1044G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1044 | chr6 | 7882100 | ||||||
| chr6:7882213 | C | T | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*931G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 931 | chr6 | 7882213 | ||||||
| chr6:7882276 | G | C | 1 | a0001c0001t0011 | 2 | HG02572.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*868C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 868 | chr6 | 7882276 | ||||||
| chr6:7882412 | G | A | 1 | a0001c0001t0018 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 732 | chr6 | 7882412 | ||||||
| chr6:7882749 | G | A | 1 | a0001c0001t0019 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 395 | chr6 | 7882749 | ||||||
| chr6:7882840 | C | T | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0020 others(1): Show |
34 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*304G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 304 | chr6 | 7882840 | ||||||
| chr6:7882954 | AAACTT | A | 2 | a0001c0001t0009 a0001c0001t0020 |
3 | HG02165.hp1 HG03453.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*185_*189delAAGTT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 185 | chr6 | 7882954 | ||||||
| chr6:7882962 | C | T | 1 | a0001c0001t0008 | 2 | NA18952.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*182G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 182 | chr6 | 7882962 | ||||||
| chr6:7883082 | G | C | 1 | a0001c0002t0010 | 2 | HG02257.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 62 | chr6 | 7883082 | ||||||
| chr6:7910778 | G | A | 1 | a0001c0001t0022 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 2 | chr6 | 7910778 | ||||||
| chr6:7910778 | G | C | 3 | a0001c0001t0004 a0001c0001t0011 a0001c0002t0021 |
10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-2C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 2 | chr6 | 7910778 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7883286 | A | G | 3 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 |
7 | HG01109.hp2 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-20T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883286 | |||||||
| chr6:7883400 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1177-134A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883400 | |||||||
| chr6:7883442 | G | A | 1 | a0001c0001t0001g0039 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1177-176C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883442 | |||||||
| chr6:7883614 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1177-348T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883614 | |||||||
| chr6:7883632 | C | T | 1 | a0001c0001t0001g0011 | 5 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-366G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883632 | |||||||
| chr6:7883683 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0141 a0001c0001t0001g0197 |
6 | HG00558.hp2 HG00609.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177-417T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883683 | |||||||
| chr6:7883872 | T | G | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1176+487A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883872 | |||||||
| chr6:7883902 | C | T | 1 | a0002c0005t0001g0022 | 3 | HG00735.hp1 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1176+457G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883902 | |||||||
| chr6:7884003 | C | T | 1 | a0001c0001t0006g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1176+356G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884003 | |||||||
| chr6:7884009 | G | A | 25 | a0001c0001t0003g0017 a0001c0001t0003g0038 a0001c0001t0003g0041 others(22): Show |
33 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1176+350C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884009 | |||||||
| chr6:7884058 | C | T | 3 | a0001c0002t0002g0031 a0001c0002t0002g0116 a0001c0002t0002g0117 |
4 | HG00639.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176+301G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884058 | |||||||
| chr6:7884089 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1176+270C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884089 | |||||||
| chr6:7884174 | G | A | 1 | a0001c0001t0003g0147 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1176+185C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884174 | |||||||
| chr6:7884184 | G | A | 1 | a0001c0002t0002g0124 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1176+175C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884184 | |||||||
| chr6:7884218 | CCAAA | C | 6 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1176+137_1176+140d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884218 | |||||||
| chr6:7884272 | AGAGTGAG others(11): Show |
A | 1 | a0001c0001t0003g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1176+69_1176+86del others(18): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884272 | |||||||
| chr6:7884495 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02083.hp2 | splice_region_variant&intron_variant | LOW | c.1047-7G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7884495 | |||||||
| chr6:7884951 | C | A | 5 | a0001c0001t0001g0135 a0001c0001t0001g0165 a0001c0001t0001g0213 others(2): Show |
5 | HG00733.hp2 HG01256.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-463G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7884951 | |||||||
| chr6:7885021 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1047-533G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885021 | |||||||
| chr6:7885069 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(176): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.1047-581G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885069 | |||||||
| chr6:7885082 | G | C | 1 | a0001c0001t0002g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1047-594C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885082 | |||||||
| chr6:7885131 | T | C | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047-643A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885131 | |||||||
| chr6:7885285 | T | C | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1046+676A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885285 | |||||||
| chr6:7885395 | A | G | 7 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(4): Show |
9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1046+566T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885395 | |||||||
| chr6:7885428 | C | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0137 others(10): Show |
20 | HG00423.hp1 HG00544.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1046+533G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885428 | |||||||
| chr6:7885514 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1046+447G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885514 | |||||||
| chr6:7885564 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1046+397G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885564 | |||||||
| chr6:7886139 | A | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0121 a0001c0001t0002g0122 |
4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-96T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886139 | |||||||
| chr6:7886221 | T | G | 1 | a0001c0003t0001g0182 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.964-178A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886221 | |||||||
| chr6:7886301 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(123): Show |
208 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.964-258G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886301 | |||||||
| chr6:7886384 | G | T | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.964-341C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886384 | |||||||
| chr6:7886406 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(180): Show |
283 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.964-363A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886406 | |||||||
| chr6:7886500 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.964-457G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886500 | |||||||
| chr6:7886509 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.964-466A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886509 | |||||||
| chr6:7886570 | C | G | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-527G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886570 | |||||||
| chr6:7886600 | C | T | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-557G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886600 | |||||||
| chr6:7886672 | A | G | 54 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0224 others(51): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.964-629T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886672 | |||||||
| chr6:7886726 | CTA | C | 2 | a0001c0002t0002g0016 a0001c0002t0002g0126 |
5 | HG02895.hp2 HG02897.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-685_964-684del others(2): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886726 | |||||||
| chr6:7886898 | A | G | 57 | a0001c0001t0001g0075 a0001c0001t0001g0166 a0001c0001t0001g0198 others(54): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.964-855T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886898 | |||||||
| chr6:7886913 | C | T | 1 | a0001c0003t0001g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.964-870G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886913 | |||||||
| chr6:7886990 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
211 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.964-947T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886990 | |||||||
| chr6:7887104 | G | A | 52 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0001g0179 others(49): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-1061C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887104 | |||||||
| chr6:7887106 | C | CAACT | 52 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0001g0179 others(49): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-1067_964-1064d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887106 | |||||||
| chr6:7887184 | T | C | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-1141A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887184 | |||||||
| chr6:7887187 | TGTGGCCC others(19): Show |
T | 1 | a0005c0012t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.964-1170_964-1145d others(28): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887187 | |||||||
| chr6:7887371 | G | A | 6 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-1328C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887371 | |||||||
| chr6:7887419 | C | T | 2 | a0001c0004t0002g0015 a0001c0004t0002g0123 |
5 | HG01361.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+1286G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887419 | |||||||
| chr6:7887437 | CT | C | 30 | a0001c0001t0001g0224 a0001c0001t0001g0232 a0001c0001t0003g0017 others(27): Show |
39 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+1267delA | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887437 | |||||||
| chr6:7887482 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.963+1223C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887482 | |||||||
| chr6:7887501 | T | TCTC | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(180): Show |
283 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.963+1201_963+1203d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887501 | |||||||
| chr6:7887586 | G | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(182): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.963+1119C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887586 | |||||||
| chr6:7887600 | G | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0121 a0001c0001t0002g0122 |
4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1105C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887600 | |||||||
| chr6:7887633 | C | T | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.963+1072G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887633 | |||||||
| chr6:7887681 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.963+1024T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887681 | |||||||
| chr6:7887712 | C | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(180): Show |
283 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.963+993G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887712 | |||||||
| chr6:7887716 | T | C | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+989A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887716 | |||||||
| chr6:7887739 | T | A | 1 | a0001c0001t0003g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.963+966A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887739 | |||||||
| chr6:7887833 | A | G | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+872T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887833 | |||||||
| chr6:7887901 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+804G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887901 | |||||||
| chr6:7887935 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
210 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.963+770G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887935 | |||||||
| chr6:7887967 | T | A | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+738A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887967 | |||||||
| chr6:7888018 | T | C | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+687A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888018 | |||||||
| chr6:7888032 | T | C | 7 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(4): Show |
9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.963+673A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888032 | |||||||
| chr6:7888095 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(180): Show |
283 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.963+610G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888095 | |||||||
| chr6:7888312 | C | G | 1 | a0001c0001t0008g0027 | 2 | NA18952.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.963+393G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888312 | |||||||
| chr6:7888378 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.963+327T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888378 | |||||||
| chr6:7888450 | A | T | 7 | a0001c0001t0001g0227 a0001c0001t0001g0239 a0001c0001t0002g0226 others(4): Show |
7 | HG01884.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+255T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888450 | |||||||
| chr6:7888500 | G | A | 2 | a0003c0007t0001g0250 a0003c0007t0001g0251 |
2 | HG01943.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.963+205C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888500 | |||||||
| chr6:7888516 | G | A | 7 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(4): Show |
9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.963+189C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888516 | |||||||
| chr6:7888666 | G | A | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+39C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888666 | |||||||
| chr6:7888676 | T | C | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+29A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888676 | |||||||
| chr6:7888855 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(182): Show |
285 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(282): Show |
splice_region_variant&intron_variant | LOW | c.820-7T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7888855 | |||||||
| chr6:7888868 | G | A | 1 | a0001c0003t0001g0176 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.820-20C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7888868 | |||||||
| chr6:7888959 | G | A | 1 | a0010c0014t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.820-111C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7888959 | |||||||
| chr6:7889021 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.820-173G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889021 | |||||||
| chr6:7889077 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(125): Show |
207 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.820-229G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889077 | |||||||
| chr6:7889125 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.820-277T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889125 | |||||||
| chr6:7889232 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
222 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.819+263T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889232 | |||||||
| chr6:7889233 | A | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+262T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889233 | |||||||
| chr6:7889646 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.733-65T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889646 | |||||||
| chr6:7889661 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.733-80G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889661 | |||||||
| chr6:7889705 | GC | G | 7 | a0001c0001t0001g0227 a0001c0001t0001g0239 a0001c0001t0002g0226 others(4): Show |
7 | HG01884.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-125delG | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889705 | |||||||
| chr6:7889839 | T | C | 1 | a0001c0003t0001g0136 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.733-258A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889839 | |||||||
| chr6:7889888 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
222 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.733-307A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889888 | |||||||
| chr6:7889934 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0015g0194 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-353A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889934 | |||||||
| chr6:7889983 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.733-402T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889983 | |||||||
| chr6:7890039 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
194 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.733-458C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890039 | |||||||
| chr6:7890355 | C | CGG | 3 | a0001c0001t0002g0033 a0001c0001t0002g0121 a0001c0001t0002g0122 |
4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-776_733-775dup others(2): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890355 | |||||||
| chr6:7890543 | A | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(133): Show |
222 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.733-962T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890543 | |||||||
| chr6:7890619 | C | T | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.732+1002G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890619 | |||||||
| chr6:7890721 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.732+900T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890721 | |||||||
| chr6:7890754 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.732+867T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890754 | |||||||
| chr6:7890758 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.732+863A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890758 | |||||||
| chr6:7890773 | G | C | 1 | a0004c0006t0001g0040 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.732+848C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890773 | |||||||
| chr6:7890846 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+775C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890846 | |||||||
| chr6:7890927 | G | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
197 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.732+694C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890927 | |||||||
| chr6:7890935 | T | A | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.732+686A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890935 | |||||||
| chr6:7890997 | T | C | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.732+624A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890997 | |||||||
| chr6:7891039 | G | A | 1 | a0001c0001t0003g0246 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.732+582C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891039 | |||||||
| chr6:7891050 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.732+571C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891050 | |||||||
| chr6:7891151 | T | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+470A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891151 | |||||||
| chr6:7891170 | T | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0082 others(14): Show |
23 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+451A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891170 | |||||||
| chr6:7891281 | C | T | 1 | a0001c0001t0001g0011 | 5 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+340G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891281 | |||||||
| chr6:7891292 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.732+329C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891292 | |||||||
| chr6:7891317 | T | G | 2 | a0001c0002t0010g0118 a0001c0002t0010g0183 |
2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.732+304A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891317 | |||||||
| chr6:7891356 | C | T | 1 | a0001c0001t0019g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.732+265G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891356 | |||||||
| chr6:7891440 | G | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0165 a0001c0001t0001g0213 others(2): Show |
5 | HG00733.hp2 HG01256.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+181C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891440 | |||||||
| chr6:7891449 | A | C | 14 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0002g0016 others(11): Show |
23 | HG01081.hp1 HG01361.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.732+172T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891449 | |||||||
| chr6:7891541 | C | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.732+80G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891541 | |||||||
| chr6:7891542 | G | A | 38 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0232 others(35): Show |
47 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.732+79C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891542 | |||||||
| chr6:7891543 | G | T | 1 | a0008c0008t0002g0056 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.732+78C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891543 | |||||||
| chr6:7891570 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.732+51A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891570 | |||||||
| chr6:7891910 | C | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(176): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.617-174G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7891910 | |||||||
| chr6:7891918 | C | T | 2 | a0001c0001t0002g0168 a0001c0001t0003g0147 |
2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.617-182G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7891918 | |||||||
| chr6:7892000 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.617-264T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892000 | |||||||
| chr6:7892014 | C | T | 1 | a0001c0001t0005g0178 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.617-278G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892014 | |||||||
| chr6:7892090 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.617-354C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892090 | |||||||
| chr6:7892092 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.617-356T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892092 | |||||||
| chr6:7892220 | GTCT | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0199 |
5 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-487_617-485del others(3): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892220 | |||||||
| chr6:7892342 | G | A | 38 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0232 others(35): Show |
47 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.617-606C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892342 | |||||||
| chr6:7892589 | G | A | 4 | a0001c0003t0001g0032 a0001c0003t0001g0043 a0001c0003t0001g0156 others(1): Show |
6 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.617-853C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892589 | |||||||
| chr6:7892718 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617-982A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892718 | |||||||
| chr6:7892789 | A | T | 14 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0002g0016 others(11): Show |
23 | HG01081.hp1 HG01361.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.617-1053T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892789 | |||||||
| chr6:7892832 | G | A | 7 | a0001c0001t0001g0221 a0001c0002t0001g0120 a0001c0002t0001g0134 others(4): Show |
9 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.617-1096C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892832 | |||||||
| chr6:7892854 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.617-1118T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892854 | |||||||
| chr6:7892930 | T | C | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.617-1194A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892930 | |||||||
| chr6:7892942 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.617-1206C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892942 | |||||||
| chr6:7893054 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
197 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.617-1318T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893054 | |||||||
| chr6:7893094 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.617-1358G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893094 | |||||||
| chr6:7893169 | T | C | 1 | a0001c0001t0006g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.617-1433A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893169 | |||||||
| chr6:7893240 | C | G | 6 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-1504G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893240 | |||||||
| chr6:7893385 | G | A | 5 | a0001c0001t0002g0168 a0001c0001t0003g0041 a0001c0001t0003g0147 others(2): Show |
6 | HG01243.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.617-1649C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893385 | |||||||
| chr6:7893489 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0096 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.616+1617G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893489 | |||||||
| chr6:7893490 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.616+1616C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893490 | |||||||
| chr6:7893497 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.616+1609G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893497 | |||||||
| chr6:7893535 | G | GCCTGCCG others(12): Show |
2 | a0001c0001t0001g0239 a0001c0001t0002g0033 |
3 | HG01891.hp2 HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.616+1552_616+1570d others(21): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893535 | |||||||
| chr6:7893550 | T | C | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.616+1556A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893550 | |||||||
| chr6:7893651 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.616+1455G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893651 | |||||||
| chr6:7893664 | T | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0141 a0001c0001t0001g0170 others(1): Show |
7 | HG00558.hp2 HG00609.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.616+1442A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893664 | |||||||
| chr6:7893668 | G | A | 1 | a0001c0010t0001g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.616+1438C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893668 | |||||||
| chr6:7893676 | G | A | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.616+1430C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893676 | |||||||
| chr6:7893695 | CTT | C | 2 | a0001c0001t0003g0055 a0001c0001t0003g0241 |
3 | HG00280.hp1 HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.616+1409_616+1410d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893695 | |||||||
| chr6:7893732 | A | G | 1 | a0001c0001t0013g0146 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.616+1374T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893732 | |||||||
| chr6:7893781 | A | C | 7 | a0001c0001t0004g0023 a0001c0001t0004g0254 a0001c0001t0004g0255 others(4): Show |
9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.616+1325T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893781 | |||||||
| chr6:7893837 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.616+1269G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893837 | |||||||
| chr6:7893849 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.616+1257C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893849 | |||||||
| chr6:7893920 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.616+1186G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893920 | |||||||
| chr6:7894089 | A | G | 1 | a0001c0001t0008g0027 | 2 | NA18952.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.616+1017T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894089 | |||||||
| chr6:7894249 | C | T | 1 | a0001c0003t0001g0156 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.616+857G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894249 | |||||||
| chr6:7894453 | A | C | 1 | a0001c0001t0001g0035 | 2 | NA19000.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.616+653T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894453 | |||||||
| chr6:7894462 | T | C | 16 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(13): Show |
28 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.616+644A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894462 | |||||||
| chr6:7894561 | G | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
219 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.616+545C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894561 | |||||||
| chr6:7894947 | G | A | 1 | a0001c0001t0005g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.616+159C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894947 | |||||||
| chr6:7895087 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.616+19T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7895087 | |||||||
| chr6:7895342 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.520-140C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895342 | |||||||
| chr6:7895655 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0049 others(2): Show |
9 | HG00423.hp2 HG00558.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-453G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895655 | |||||||
| chr6:7895673 | A | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0177 a0001c0002t0001g0152 others(2): Show |
6 | HG01884.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-471T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895673 | |||||||
| chr6:7895680 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0035 others(55): Show |
101 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.520-478C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895680 | |||||||
| chr6:7895747 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0163 |
2 | HG02083.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.520-545A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895747 | |||||||
| chr6:7895837 | A | C | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.520-635T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895837 | |||||||
| chr6:7895837 | A | T | 4 | a0001c0001t0001g0227 a0001c0001t0002g0226 a0001c0001t0002g0228 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-635T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895837 | |||||||
| chr6:7895862 | G | A | 1 | a0001c0002t0010g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.520-660C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895862 | |||||||
| chr6:7895908 | A | G | 4 | a0001c0001t0005g0044 a0001c0001t0005g0173 a0001c0001t0005g0184 others(1): Show |
5 | HG00609.hp2 HG02080.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-706T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895908 | |||||||
| chr6:7896258 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
313 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.520-1056T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896258 | |||||||
| chr6:7896557 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.520-1355C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896557 | |||||||
| chr6:7896710 | G | A | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.520-1508C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896710 | |||||||
| chr6:7896779 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.520-1577G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896779 | |||||||
| chr6:7896826 | G | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1624C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896826 | |||||||
| chr6:7896830 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(237): Show |
367 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.520-1628A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896830 | |||||||
| chr6:7897167 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(234): Show |
363 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.520-1965G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897167 | |||||||
| chr6:7897554 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0189 |
2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.519+2022G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897554 | |||||||
| chr6:7897634 | T | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+1942A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897634 | |||||||
| chr6:7897658 | C | T | 1 | a0001c0001t0003g0055 | 2 | HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.519+1918G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897658 | |||||||
| chr6:7897777 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0187 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.519+1799A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897777 | |||||||
| chr6:7897853 | A | T | 1 | a0001c0002t0007g0019 | 3 | HG03041.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.519+1723T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897853 | |||||||
| chr6:7897914 | A | G | 41 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0232 others(38): Show |
51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.519+1662T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897914 | |||||||
| chr6:7898018 | G | A | 3 | a0001c0001t0015g0194 a0001c0002t0007g0019 a0001c0002t0007g0119 |
5 | HG02647.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+1558C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898018 | |||||||
| chr6:7898063 | G | GT | 8 | a0001c0001t0001g0201 a0001c0001t0002g0102 a0001c0001t0003g0245 others(5): Show |
8 | HG02080.hp1 HG02300.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+1512dupA | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898063 | |||||||
| chr6:7898414 | T | C | 3 | a0001c0002t0007g0019 a0001c0002t0007g0119 a0001c0002t0021g0253 |
5 | HG02647.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+1162A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898414 | |||||||
| chr6:7898530 | G | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+1046C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898530 | |||||||
| chr6:7898642 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(176): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.519+934T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898642 | |||||||
| chr6:7898681 | C | T | 1 | a0007c0013t0001g0154 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.519+895G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898681 | |||||||
| chr6:7898694 | C | T | 1 | a0010c0014t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.519+882G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898694 | |||||||
| chr6:7898739 | C | G | 1 | a0001c0001t0003g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.519+837G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898739 | |||||||
| chr6:7898773 | CATG | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.519+800_519+802del others(3): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898773 | |||||||
| chr6:7898900 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.519+676C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898900 | |||||||
| chr6:7899161 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.519+415C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899161 | |||||||
| chr6:7899215 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.519+361G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899215 | |||||||
| chr6:7899295 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(177): Show |
280 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.519+281A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899295 | |||||||
| chr6:7899315 | A | G | 14 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0002g0016 others(11): Show |
23 | HG01081.hp1 HG01361.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.519+261T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899315 | |||||||
| chr6:7899336 | C | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.519+240G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899336 | |||||||
| chr6:7899340 | G | T | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+236C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899340 | |||||||
| chr6:7899352 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.519+224G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899352 | |||||||
| chr6:7899380 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.519+196G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899380 | |||||||
| chr6:7899418 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(169): Show |
267 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.519+158C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899418 | |||||||
| chr6:7899424 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(176): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.519+152G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899424 | |||||||
| chr6:7899532 | A | AGAGGGAG others(1): Show |
45 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0232 others(42): Show |
57 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.519+36_519+43dupCC others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | |||||||
| chr6:7899532 | A | AGAGGGAG others(5): Show |
6 | a0001c0001t0002g0226 a0001c0001t0004g0255 a0001c0002t0002g0016 others(3): Show |
10 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.519+32_519+43dupCC others(10): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | |||||||
| chr6:7899532 | A | AGAGGGAG others(9): Show |
3 | a0001c0001t0004g0256 a0001c0001t0004g0258 a0001c0004t0002g0015 |
6 | HG02451.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+28_519+43dupCC others(14): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | |||||||
| chr6:7899532 | A | AGAGGGAG others(13): Show |
1 | a0001c0004t0002g0123 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.519+24_519+43dupCC others(18): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | |||||||
| chr6:7899532 | AGAGGGAG others(1): Show |
A | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+36_519+43delCC others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | |||||||
| chr6:7899691 | T | A | 1 | a0001c0001t0006g0217 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.414-10A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899691 | |||||||
| chr6:7899757 | A | G | 1 | a0001c0001t0003g0237 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.414-76T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899757 | |||||||
| chr6:7899795 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
218 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.414-114A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899795 | |||||||
| chr6:7899958 | A | T | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414-277T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899958 | |||||||
| chr6:7900067 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.414-386T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900067 | |||||||
| chr6:7900069 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.414-388C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900069 | |||||||
| chr6:7900212 | C | G | 2 | a0001c0002t0002g0116 a0001c0002t0002g0117 |
2 | HG00639.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.414-531G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900212 | |||||||
| chr6:7900252 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(114): Show |
193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.414-571A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900252 | |||||||
| chr6:7900476 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
228 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.414-795T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900476 | |||||||
| chr6:7900554 | G | A | 1 | a0001c0001t0005g0173 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.414-873C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900554 | |||||||
| chr6:7900623 | C | T | 7 | a0001c0001t0004g0023 a0001c0001t0004g0254 a0001c0001t0004g0255 others(4): Show |
9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-942G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900623 | |||||||
| chr6:7900716 | C | T | 6 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-1035G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900716 | |||||||
| chr6:7900726 | C | T | 6 | a0001c0002t0001g0120 a0001c0002t0001g0134 a0001c0002t0007g0019 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-1045G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900726 | |||||||
| chr6:7900954 | C | CA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(113): Show |
192 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.414-1274dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900954 | |||||||
| chr6:7900954 | CA | C | 3 | a0001c0001t0001g0095 a0001c0002t0007g0019 a0001c0002t0007g0119 |
5 | HG02258.hp2 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-1274delT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900954 | |||||||
| chr6:7900971 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414-1290A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900971 | |||||||
| chr6:7901085 | G | T | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.414-1404C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901085 | |||||||
| chr6:7901219 | A | G | 3 | a0001c0002t0001g0152 a0001c0002t0001g0174 a0001c0002t0001g0175 |
3 | HG03098.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.414-1538T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901219 | |||||||
| chr6:7901227 | G | A | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.414-1546C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901227 | |||||||
| chr6:7901290 | C | T | 2 | a0001c0002t0007g0019 a0001c0002t0007g0119 |
4 | HG02647.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-1609G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901290 | |||||||
| chr6:7901422 | A | G | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-1741T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901422 | |||||||
| chr6:7901430 | G | GTA | 7 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.414-1751_414-1750d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901430 | |||||||
| chr6:7901476 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414-1795T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901476 | |||||||
| chr6:7901561 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.414-1880C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901561 | |||||||
| chr6:7901651 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.414-1970C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901651 | |||||||
| chr6:7901714 | C | T | 23 | a0001c0001t0001g0224 a0001c0001t0001g0232 a0001c0001t0003g0017 others(20): Show |
29 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.414-2033G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901714 | |||||||
| chr6:7901839 | G | T | 1 | a0001c0001t0005g0184 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.414-2158C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901839 | |||||||
| chr6:7901943 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(112): Show |
191 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.414-2262C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901943 | |||||||
| chr6:7902042 | G | C | 5 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(2): Show |
9 | HG01109.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-2361C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902042 | |||||||
| chr6:7902133 | G | A | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+2441C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902133 | |||||||
| chr6:7902234 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0015g0194 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.413+2340A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902234 | |||||||
| chr6:7902298 | G | A | 8 | a0001c0001t0001g0133 a0001c0001t0002g0010 a0001c0001t0002g0102 others(5): Show |
13 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+2276C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902298 | |||||||
| chr6:7902409 | GCC | G | 8 | a0001c0001t0001g0133 a0001c0001t0002g0010 a0001c0001t0002g0102 others(5): Show |
13 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+2163_413+2164d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902409 | |||||||
| chr6:7902469 | G | A | 1 | a0001c0002t0002g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.413+2105C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902469 | |||||||
| chr6:7902706 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.413+1868C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902706 | |||||||
| chr6:7902724 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.413+1850C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902724 | |||||||
| chr6:7902813 | A | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+1761T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902813 | |||||||
| chr6:7902872 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+1702G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902872 | |||||||
| chr6:7902882 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(113): Show |
192 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.413+1692A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902882 | |||||||
| chr6:7902959 | G | A | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+1615C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902959 | |||||||
| chr6:7903151 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
399 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(396): Show |
intron_variant | MODIFIER | c.413+1423A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903151 | |||||||
| chr6:7903233 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0035 others(49): Show |
93 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.413+1341G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903233 | |||||||
| chr6:7903274 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0018 others(18): Show |
33 | HG00099.hp1 HG00597.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+1300C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903274 | |||||||
| chr6:7903284 | ATAG | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
214 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.413+1287_413+1289d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903284 | |||||||
| chr6:7903396 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(106): Show |
185 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.413+1178C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903396 | |||||||
| chr6:7903774 | T | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0139 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+800A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903774 | |||||||
| chr6:7903893 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02145.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+681A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903893 | |||||||
| chr6:7903932 | T | G | 1 | a0001c0002t0001g0174 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.413+642A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903932 | |||||||
| chr6:7904075 | T | C | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+499A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904075 | |||||||
| chr6:7904213 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0029 |
6 | NA18939.hp2 NA18942.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+361C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904213 | |||||||
| chr6:7904241 | G | A | 1 | a0001c0001t0001g0048 | 2 | NA18612.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.413+333C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904241 | |||||||
| chr6:7904443 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.413+131T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904443 | |||||||
| chr6:7904556 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413+18G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904556 | |||||||
| chr6:7904836 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0011g0259 |
2 | HG02572.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.264-113A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7904836 | |||||||
| chr6:7904951 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.264-228A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7904951 | |||||||
| chr6:7905036 | C | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0139 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-313G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905036 | |||||||
| chr6:7905091 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-368A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905091 | |||||||
| chr6:7905292 | A | T | 2 | a0001c0004t0002g0015 a0001c0004t0002g0123 |
5 | HG01361.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-569T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905292 | |||||||
| chr6:7905300 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.264-577G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905300 | |||||||
| chr6:7905467 | C | G | 1 | a0008c0008t0002g0056 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264-744G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905467 | |||||||
| chr6:7905786 | G | T | 1 | a0008c0008t0002g0056 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264-1063C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905786 | |||||||
| chr6:7905809 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.264-1086C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905809 | |||||||
| chr6:7905919 | T | C | 23 | a0001c0001t0001g0224 a0001c0001t0001g0232 a0001c0001t0003g0017 others(20): Show |
29 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.264-1196A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905919 | |||||||
| chr6:7906086 | AAAAAATT others(49): Show |
A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0121 a0001c0001t0002g0122 |
4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1419_264-1364d others(58): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906086 | |||||||
| chr6:7906139 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264-1416C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906139 | |||||||
| chr6:7906235 | T | A | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264-1512A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906235 | |||||||
| chr6:7906267 | G | A | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-1544C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906267 | |||||||
| chr6:7906333 | C | T | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-1610G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906333 | |||||||
| chr6:7906424 | T | C | 39 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0232 others(36): Show |
51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.264-1701A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906424 | |||||||
| chr6:7906425 | A | G | 39 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0232 others(36): Show |
51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.264-1702T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906425 | |||||||
| chr6:7906458 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.264-1735G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906458 | |||||||
| chr6:7906511 | G | A | 1 | a0001c0001t0004g0255 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.264-1788C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906511 | |||||||
| chr6:7906515 | G | A | 34 | a0001c0001t0001g0094 a0001c0001t0001g0224 a0001c0001t0001g0227 others(31): Show |
41 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.264-1792C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906515 | |||||||
| chr6:7906535 | C | CA | 30 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0060 others(27): Show |
37 | HG00544.hp2 HG01123.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.264-1813dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | |||||||
| chr6:7906535 | C | CAA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(64): Show |
125 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.264-1814_264-1813d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | |||||||
| chr6:7906535 | C | CAAA | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0049 others(23): Show |
37 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.264-1815_264-1813d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | |||||||
| chr6:7906535 | C | CAAAA | 7 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(4): Show |
7 | HG01109.hp1 HG02129.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-1816_264-1813d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | |||||||
| chr6:7906553 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-1830T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906553 | |||||||
| chr6:7906556 | AAG | A | 6 | a0001c0001t0002g0010 a0001c0001t0002g0103 a0001c0002t0002g0016 others(3): Show |
13 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-1835_264-1834d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906556 | |||||||
| chr6:7906557 | A | AAAC | 7 | a0001c0001t0004g0023 a0001c0001t0004g0254 a0001c0001t0004g0255 others(4): Show |
9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1835_264-1834i others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906557 | |||||||
| chr6:7906557 | AG | A | 12 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0003g0054 others(9): Show |
17 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-1835delC | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906557 | |||||||
| chr6:7906558 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(157): Show |
244 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.264-1835C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906558 | |||||||
| chr6:7906604 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.264-1881T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906604 | |||||||
| chr6:7906673 | C | CAA | 13 | a0001c0002t0001g0134 a0001c0002t0002g0016 a0001c0002t0002g0034 others(10): Show |
22 | HG01081.hp1 HG01361.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.264-1952_264-1951d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906673 | |||||||
| chr6:7906764 | G | GA | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.264-2042dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906764 | |||||||
| chr6:7906906 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(109): Show |
189 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.264-2183G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906906 | |||||||
| chr6:7907021 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0222 |
2 | HG02523.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.264-2298C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907021 | |||||||
| chr6:7907165 | C | CTTTTTTT | 2 | a0001c0001t0002g0010 a0001c0001t0003g0054 |
7 | HG00438.hp1 HG01109.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-2449_264-2443d others(9): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907165 | |||||||
| chr6:7907165 | C | CTTTTTTT others(1): Show |
29 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0239 others(26): Show |
34 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.264-2450_264-2443d others(10): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907165 | |||||||
| chr6:7907165 | C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0224 a0001c0001t0002g0033 a0001c0001t0002g0121 others(2): Show |
6 | HG01891.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-2451_264-2443d others(11): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907165 | |||||||
| chr6:7907458 | C | T | 1 | a0001c0001t0006g0216 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.264-2735G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907458 | |||||||
| chr6:7907552 | T | C | 40 | a0001c0001t0001g0029 a0001c0001t0001g0224 a0001c0001t0001g0227 others(37): Show |
53 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.264-2829A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907552 | |||||||
| chr6:7907651 | G | C | 39 | a0001c0001t0001g0224 a0001c0001t0001g0227 a0001c0001t0001g0232 others(36): Show |
51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.263+2863C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907651 | |||||||
| chr6:7907727 | A | T | 13 | a0001c0002t0001g0134 a0001c0002t0002g0016 a0001c0002t0002g0034 others(10): Show |
22 | HG01081.hp1 HG01361.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.263+2787T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907727 | |||||||
| chr6:7907787 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.263+2727C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907787 | |||||||
| chr6:7907874 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(176): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.263+2640C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907874 | |||||||
| chr6:7908070 | G | C | 19 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(16): Show |
33 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.263+2444C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908070 | |||||||
| chr6:7908112 | A | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02615.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.263+2402T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908112 | |||||||
| chr6:7908196 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.263+2318A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908196 | |||||||
| chr6:7908228 | A | T | 2 | a0001c0002t0002g0116 a0001c0002t0002g0117 |
2 | HG00639.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.263+2286T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908228 | |||||||
| chr6:7908237 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
198 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.263+2277A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908237 | |||||||
| chr6:7908281 | C | CA | 8 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0113 others(5): Show |
8 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.263+2232dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | |||||||
| chr6:7908281 | CA | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
194 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.263+2232delT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | |||||||
| chr6:7908281 | CAA | C | 16 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(13): Show |
22 | HG01081.hp1 HG01257.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.263+2231_263+2232d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | |||||||
| chr6:7908281 | CAAA | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.263+2230_263+2232d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | |||||||
| chr6:7908518 | T | TA | 36 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(33): Show |
43 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.263+1995dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908518 | |||||||
| chr6:7908518 | T | TAA | 7 | a0001c0001t0004g0023 a0001c0001t0004g0254 a0001c0001t0004g0255 others(4): Show |
9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.263+1994_263+1995d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908518 | |||||||
| chr6:7908518 | TA | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
195 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+1995delT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908518 | |||||||
| chr6:7908522 | A | C | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.263+1992T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908522 | |||||||
| chr6:7908620 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.263+1894C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908620 | |||||||
| chr6:7908829 | T | G | 1 | a0001c0003t0001g0211 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.263+1685A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908829 | |||||||
| chr6:7908963 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA18942.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.263+1551C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908963 | |||||||
| chr6:7909101 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(115): Show |
195 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+1413C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909101 | |||||||
| chr6:7909108 | T | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
299 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.263+1406A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909108 | |||||||
| chr6:7909226 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0110 others(38): Show |
55 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.263+1288C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909226 | |||||||
| chr6:7909273 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0104 others(4): Show |
14 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+1241A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909273 | |||||||
| chr6:7909373 | TCTGG | T | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+1137_263+1140d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909373 | |||||||
| chr6:7909475 | G | A | 2 | a0001c0003t0001g0210 a0001c0003t0001g0211 |
2 | NA18977.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.263+1039C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909475 | |||||||
| chr6:7909523 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0019g0131 |
3 | HG02615.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.263+991G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909523 | |||||||
| chr6:7909587 | T | A | 2 | a0001c0001t0001g0213 a0001c0001t0014g0212 |
2 | HG00733.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.263+927A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909587 | |||||||
| chr6:7909690 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.263+824T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909690 | |||||||
| chr6:7909734 | C | T | 68 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(65): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.263+780G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909734 | |||||||
| chr6:7909811 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+703T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909811 | |||||||
| chr6:7909890 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.263+624G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909890 | |||||||
| chr6:7909928 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.263+586G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909928 | |||||||
| chr6:7909941 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.263+573G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909941 | |||||||
| chr6:7909999 | T | C | 13 | a0001c0001t0002g0033 a0001c0001t0002g0121 a0001c0001t0002g0122 others(10): Show |
16 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+515A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909999 | |||||||
| chr6:7910064 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.263+450C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910064 | |||||||
| chr6:7910080 | G | A | 8 | a0001c0002t0002g0016 a0001c0002t0002g0034 a0001c0002t0002g0124 others(5): Show |
15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+434C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910080 | |||||||
| chr6:7910093 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.263+421C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910093 | |||||||
| chr6:7910119 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
287 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.263+395T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910119 | |||||||
| chr6:7910144 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.263+370G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910144 | |||||||
| chr6:7910165 | C | G | 1 | a0001c0001t0001g0035 | 2 | NA19000.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.263+349G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910165 | |||||||
| chr6:7910202 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
288 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.263+312A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910202 | |||||||
| chr6:7910266 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.263+248G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910266 | |||||||
| chr6:7910273 | GC | G | 8 | a0001c0001t0004g0023 a0001c0001t0004g0254 a0001c0001t0004g0255 others(5): Show |
10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.263+240delG | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910273 | |||||||
| chr6:7910275 | C | T | 8 | a0001c0001t0004g0023 a0001c0001t0004g0254 a0001c0001t0004g0255 others(5): Show |
10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.263+239G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910275 | |||||||
| chr6:7910284 | C | T | 1 | a0006c0011t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.263+230G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910284 | |||||||
| chr6:7910312 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(113): Show |
192 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.263+202C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910312 | |||||||
| chr6:7910329 | C | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0219 a0001c0001t0001g0220 others(38): Show |
54 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.263+185G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910329 | |||||||
| chr6:7910366 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.263+148G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910366 | |||||||
| chr6:7910431 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.263+83C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910431 | |||||||
| chr6:7910497 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.263+17C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910497 |