Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51061 |
| ensemblid | ENSG00000153066.13 |
| hgncid | 28030 |
| symbol | TXNDC11 |
| name | thioredoxin domain containing 11 |
| refseq_nuc | NM_015914.7 |
| refseq_prot | NP_056998.4 |
| ensembl_nuc | ENST00000283033.10 |
| ensembl_prot | ENSP00000283033.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 11679083 |
| end | 11742857 |
| strand | - |
| ver | v1.2 |
| region | chr16:11679083-11742857 |
| region5000 | chr16:11674083-11747857 |
| regionname0 | TXNDC11_chr16_11679083_11742857 |
| regionname5000 | TXNDC11_chr16_11674083_11747857 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 958 | 170 | 33 | 23 | 85 | 9 | 20 | 67 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0002 | 1/0 | 958 | 96 | 36 | 15 | 32 | 2 | 10 | 24 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0003 | 0/1 | 958 | 84 | 1 | 23 | 42 | 6 | 11 | 29 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0004 | 0/0 | 958 | 6 | 0 | 0 | 5 | 0 | 1 | 5 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0005 | 0/0 | 958 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0006 | 0/0 | 958 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0007 | 0/0 | 958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0008 | 0/0 | 958 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0009 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0010 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0011 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0012 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0013 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0014 | 0/0 | 958 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0015 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0016 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| a0017 | 0/0 | 958 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | MSECG others(953): Show |
chr16 | 11674083 | 11747857 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2874 | 129 | 25 | 22 | 60 | 9 | 13 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0004 | 0/0 | 2874 | 28 | 2 | 0 | 19 | 0 | 7 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0007 | 0/0 | 2874 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0008 | 0/0 | 2874 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0014 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0017 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0018 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0024 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0001c0025 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0002c0003 | 1/0 | 2874 | 76 | 19 | 14 | 30 | 2 | 10 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0002c0005 | 0/0 | 2874 | 15 | 14 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0002c0011 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0002c0012 | 0/0 | 2874 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0002c0023 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0003c0002 | 0/1 | 2874 | 84 | 1 | 23 | 42 | 6 | 11 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0004c0006 | 0/0 | 2874 | 6 | 0 | 0 | 5 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0005c0009 | 0/0 | 2874 | 3 | 2 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0006c0010 | 0/0 | 2874 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0007c0013 | 0/0 | 2874 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0008c0019 | 0/0 | 2874 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0009c0015 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0010c0028 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0011c0021 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0012c0020 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0013c0027 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0014c0022 | 0/0 | 2874 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0015c0026 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0016c0016 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 | ||
| a0017c0029 | 0/0 | 2874 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | ATGTC others(2869): Show |
chr16 | 11674083 | 11747857 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3116 | 129 | 25 | 22 | 60 | 9 | 13 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0004t0001 | 0/0 | 3116 | 28 | 2 | 0 | 19 | 0 | 7 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0007t0001 | 0/0 | 3116 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0008t0001 | 0/0 | 3116 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0014t0001 | 0/0 | 3116 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0017t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0018t0001 | 0/0 | 3116 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0024t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0001c0025t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0002c0003t0001 | 1/0 | 3116 | 72 | 19 | 14 | 26 | 2 | 10 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0002c0003t0002 | 0/0 | 3116 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0002c0005t0001 | 0/0 | 3116 | 15 | 14 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0002c0011t0001 | 0/0 | 3116 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0002c0012t0001 | 0/0 | 3116 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0002c0023t0001 | 0/0 | 3116 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0003c0002t0001 | 0/1 | 3116 | 83 | 1 | 23 | 42 | 6 | 10 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0003c0002t0003 | 0/0 | 3116 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0004c0006t0001 | 0/0 | 3116 | 6 | 0 | 0 | 5 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0005c0009t0001 | 0/0 | 3116 | 3 | 2 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0006c0010t0001 | 0/0 | 3116 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0007c0013t0001 | 0/0 | 3116 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0008c0019t0001 | 0/0 | 3116 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0009c0015t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0010c0028t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0011c0021t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0012c0020t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0013c0027t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0014c0022t0001 | 0/0 | 3116 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0015c0026t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0016c0016t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| a0017c0029t0001 | 0/0 | 3116 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | GCGGC others(3111): Show |
chr16 | 11674083 | 11747857 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0007t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0008t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0014t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0014t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0017t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0018t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0024t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0001c0025t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0005t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0011t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0011t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0012t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0012t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0002c0023t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0289 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0003c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0004c0006t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0004c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0004c0006t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0004c0006t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0005c0009t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0005c0009t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0005c0009t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0006c0010t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0006c0010t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0006c0010t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0007c0013t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0007c0013t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0008c0019t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0009c0015t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0010c0028t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0011c0021t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0012c0020t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0013c0027t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0014c0022t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0015c0026t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0016c0016t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| a0017c0029t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0002 | t0001 | g0006 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00099 | hp2 | a0008 | c0019 | t0001 | g0085 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00140 | hp1 | a0003 | c0002 | t0001 | g0303 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00140 | hp2 | a0003 | c0002 | t0001 | g0023 | EUR | GBR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00280 | hp1 | a0003 | c0002 | t0001 | g0021 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00323 | hp1 | a0003 | c0002 | t0001 | g0278 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0064 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0165 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00423 | hp1 | a0002 | c0003 | t0001 | g0205 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00423 | hp2 | a0003 | c0002 | t0001 | g0318 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00544 | hp1 | a0001 | c0004 | t0001 | g0062 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0239 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00597 | hp1 | a0003 | c0002 | t0001 | g0333 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00621 | hp1 | a0009 | c0015 | t0001 | g0026 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0170 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00673 | hp1 | a0003 | c0002 | t0001 | g0319 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00733 | hp2 | a0003 | c0002 | t0001 | g0290 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00735 | hp1 | a0003 | c0002 | t0001 | g0304 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00735 | hp2 | a0003 | c0002 | t0001 | g0297 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0136 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01070 | hp1 | a0003 | c0002 | t0001 | g0338 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0149 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01074 | hp2 | a0003 | c0002 | t0001 | g0006 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01081 | hp2 | a0003 | c0002 | t0001 | g0282 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01099 | hp1 | a0003 | c0002 | t0001 | g0277 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0143 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01106 | hp1 | a0003 | c0002 | t0001 | g0023 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01106 | hp2 | a0003 | c0002 | t0001 | g0299 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0188 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01109 | hp2 | a0001 | c0007 | t0001 | g0008 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0145 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01168 | hp1 | a0003 | c0002 | t0001 | g0332 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01169 | hp2 | a0003 | c0002 | t0001 | g0283 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0184 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0192 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0151 | AMR | PUR | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01255 | hp2 | a0003 | c0002 | t0001 | g0306 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01256 | hp2 | a0003 | c0002 | t0001 | g0308 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01261 | hp2 | a0002 | c0005 | t0001 | g0038 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01346 | hp1 | a0003 | c0002 | t0001 | g0001 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01358 | hp2 | a0003 | c0002 | t0001 | g0292 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01361 | hp1 | a0003 | c0002 | t0001 | g0293 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01433 | hp2 | a0003 | c0002 | t0001 | g0334 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01496 | hp1 | a0005 | c0009 | t0001 | g0247 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0180 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0191 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01884 | hp2 | a0001 | c0007 | t0001 | g0029 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01891 | hp2 | a0002 | c0005 | t0001 | g0043 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01934 | hp1 | a0003 | c0002 | t0001 | g0309 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0152 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01952 | hp1 | a0003 | c0002 | t0001 | g0001 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0194 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01978 | hp1 | a0003 | c0002 | t0001 | g0324 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0200 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01981 | hp2 | a0003 | c0002 | t0001 | g0025 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0148 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02015 | hp1 | a0001 | c0004 | t0001 | g0051 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02015 | hp2 | a0003 | c0002 | t0001 | g0280 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02027 | hp1 | a0003 | c0002 | t0001 | g0274 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0047 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02055 | hp2 | a0002 | c0023 | t0001 | g0084 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0053 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02056 | hp2 | a0003 | c0002 | t0001 | g0330 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0196 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02083 | hp1 | a0003 | c0002 | t0001 | g0272 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0162 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02132 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02135 | hp1 | a0003 | c0002 | t0001 | g0320 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0163 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02155 | hp2 | a0003 | c0002 | t0001 | g0325 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02165 | hp1 | a0001 | c0008 | t0001 | g0221 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | CDX | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0179 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0153 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02273 | hp2 | a0003 | c0002 | t0001 | g0315 | AMR | PEL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0131 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02523 | hp1 | a0003 | c0002 | t0001 | g0307 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02572 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02615 | hp2 | a0006 | c0010 | t0001 | g0267 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02622 | hp1 | a0001 | c0014 | t0001 | g0073 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0031 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0138 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02683 | hp2 | a0002 | c0003 | t0001 | g0254 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02717 | hp2 | a0002 | c0005 | t0001 | g0044 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02723 | hp1 | a0002 | c0005 | t0001 | g0045 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0139 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02738 | hp1 | a0003 | c0002 | t0001 | g0335 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0198 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02809 | hp1 | a0005 | c0009 | t0001 | g0224 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0142 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02818 | hp1 | a0002 | c0005 | t0001 | g0040 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02886 | hp1 | a0002 | c0005 | t0001 | g0009 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0190 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02895 | hp1 | a0002 | c0005 | t0001 | g0034 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02896 | hp1 | a0005 | c0009 | t0001 | g0244 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02896 | hp2 | a0002 | c0005 | t0001 | g0039 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02922 | hp1 | a0002 | c0005 | t0001 | g0035 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0117 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0135 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03017 | hp1 | a0001 | c0004 | t0001 | g0066 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03017 | hp2 | a0002 | c0003 | t0001 | g0140 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03041 | hp1 | a0006 | c0010 | t0001 | g0266 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0160 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0032 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0181 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03130 | hp2 | a0002 | c0005 | t0001 | g0009 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0175 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0042 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0132 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0178 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03225 | hp2 | a0002 | c0005 | t0001 | g0033 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03239 | hp1 | a0001 | c0004 | t0001 | g0057 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0041 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0133 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03486 | hp2 | a0007 | c0013 | t0001 | g0116 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03490 | hp2 | a0002 | c0003 | t0001 | g0137 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03491 | hp1 | a0003 | c0002 | t0003 | g0288 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0059 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03492 | hp2 | a0003 | c0002 | t0001 | g0287 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03516 | hp1 | a0007 | c0013 | t0001 | g0115 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03516 | hp2 | a0002 | c0005 | t0001 | g0036 | AFR | ESN | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03540 | hp1 | a0002 | c0011 | t0001 | g0068 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0187 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03669 | hp1 | a0003 | c0002 | t0001 | g0298 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03688 | hp1 | a0003 | c0002 | t0001 | g0310 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0202 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03704 | hp2 | a0003 | c0002 | t0001 | g0286 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0058 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0201 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03834 | hp1 | a0003 | c0002 | t0001 | g0295 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0049 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0065 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03927 | hp2 | a0003 | c0002 | t0001 | g0279 | SAS | BEB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04115 | hp1 | a0003 | c0002 | t0001 | g0305 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0141 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04204 | hp2 | a0003 | c0002 | t0001 | g0021 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0052 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG04228 | hp2 | a0003 | c0002 | t0001 | g0296 | SAS | STU | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0176 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18522 | hp2 | a0002 | c0011 | t0001 | g0067 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18612 | hp1 | a0003 | c0002 | t0001 | g0316 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0161 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18747 | hp2 | a0003 | c0002 | t0001 | g0326 | EAS | CHB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18906 | hp1 | a0006 | c0010 | t0001 | g0268 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18940 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18941 | hp1 | a0003 | c0002 | t0001 | g0300 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18941 | hp2 | a0010 | c0028 | t0001 | g0269 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18942 | hp2 | a0003 | c0002 | t0001 | g0312 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18943 | hp1 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0050 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18946 | hp2 | a0003 | c0002 | t0001 | g0314 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18947 | hp2 | a0003 | c0002 | t0001 | g0323 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18948 | hp1 | a0003 | c0002 | t0001 | g0276 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18948 | hp2 | a0011 | c0021 | t0001 | g0155 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18949 | hp2 | a0001 | c0017 | t0001 | g0048 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18951 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18951 | hp2 | a0002 | c0012 | t0001 | g0168 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18952 | hp1 | a0003 | c0002 | t0001 | g0301 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0167 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18953 | hp2 | a0004 | c0006 | t0001 | g0337 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18954 | hp1 | a0003 | c0002 | t0001 | g0329 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18954 | hp2 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0164 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18957 | hp2 | a0003 | c0002 | t0001 | g0317 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0146 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0173 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18961 | hp2 | a0003 | c0002 | t0001 | g0328 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18965 | hp2 | a0003 | c0002 | t0001 | g0313 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18966 | hp2 | a0003 | c0002 | t0001 | g0025 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18970 | hp2 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18972 | hp1 | a0003 | c0002 | t0001 | g0322 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18973 | hp1 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18973 | hp2 | a0003 | c0002 | t0001 | g0311 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18975 | hp2 | a0003 | c0002 | t0001 | g0284 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18978 | hp1 | a0003 | c0002 | t0001 | g0273 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18979 | hp1 | a0012 | c0020 | t0001 | g0090 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0061 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18982 | hp1 | a0001 | c0004 | t0001 | g0055 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18984 | hp2 | a0003 | c0002 | t0001 | g0327 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18985 | hp2 | a0002 | c0003 | t0001 | g0169 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18986 | hp1 | a0004 | c0006 | t0001 | g0285 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18986 | hp2 | a0001 | c0008 | t0001 | g0220 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18988 | hp2 | a0003 | c0002 | t0001 | g0275 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0171 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18991 | hp1 | a0003 | c0002 | t0001 | g0336 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18991 | hp2 | a0001 | c0004 | t0001 | g0054 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18994 | hp1 | a0003 | c0002 | t0001 | g0302 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18994 | hp2 | a0013 | c0027 | t0001 | g0264 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19002 | hp1 | a0003 | c0002 | t0001 | g0024 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19003 | hp2 | a0003 | c0002 | t0001 | g0270 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19009 | hp1 | a0003 | c0002 | t0001 | g0271 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19010 | hp2 | a0002 | c0012 | t0001 | g0157 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0158 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19012 | hp1 | a0003 | c0002 | t0001 | g0022 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0172 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19030 | hp1 | a0001 | c0018 | t0001 | g0030 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0183 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0182 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19043 | hp2 | a0014 | c0022 | t0001 | g0166 | AFR | LWK | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19054 | hp1 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19057 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19058 | hp1 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19064 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19066 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19075 | hp2 | a0001 | c0024 | t0001 | g0076 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19079 | hp1 | a0001 | c0008 | t0001 | g0241 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19079 | hp2 | a0001 | c0025 | t0001 | g0103 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19080 | hp1 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19081 | hp1 | a0002 | c0003 | t0002 | g0069 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19082 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19082 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19084 | hp1 | a0015 | c0026 | t0001 | g0259 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19084 | hp2 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19085 | hp1 | a0016 | c0016 | t0001 | g0027 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0010 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19086 | hp1 | a0003 | c0002 | t0001 | g0281 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19088 | hp1 | a0003 | c0002 | t0001 | g0022 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19089 | hp2 | a0003 | c0002 | t0001 | g0321 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19090 | hp1 | a0017 | c0029 | t0001 | g0331 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20129 | hp2 | a0001 | c0014 | t0001 | g0120 | AFR | ASW | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0186 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0189 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20805 | hp1 | a0003 | c0002 | t0001 | g0006 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20905 | hp2 | a0004 | c0006 | t0001 | g0291 | SAS | GIH | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01123 | hp1 | a0003 | c0002 | t0001 | g0001 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0177 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0174 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0134 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02559 | hp1 | a0002 | c0005 | t0001 | g0037 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0028 | AFR | ACB | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA18955 | hp2 | a0003 | c0002 | t0001 | g0024 | EAS | JPT | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| NA20300 | hp2 | a0003 | c0002 | t0001 | g0294 | AFR | USA | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| homoSapiens | chm13v2 | a0003 | c0002 | t0001 | g0289 | REF | REF | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0156 | REF | REF | TXNDC11_chr16_11674083_11747857 | TXNDC11 | chr16 | 11674083 | 11747857 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:11679679 | C | G | 1 | a0007 | 2 | HG03486.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2393G>C | p.Gly798Ala | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 2520/3116 | 2393/2877 | 798/958 | chr16 | 11679679 | |||
| chr16:11679806 | C | G | 8 | a0001 a0004 a0005 others(5): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
missense_variant | MODERATE | c.2266G>C | p.Val756Leu | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 2393/3116 | 2266/2877 | 756/958 | chr16 | 11679806 | |||
| chr16:11687885 | G | C | 1 | a0005 | 3 | HG01496.hp1 HG02809.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.2125C>G | p.Leu709Val | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/12 | 2252/3116 | 2125/2877 | 709/958 | chr16 | 11687885 | |||
| chr16:11698246 | C | T | 1 | a0014 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.986G>A | p.Arg329Gln | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1113/3116 | 986/2877 | 329/958 | chr16 | 11698246 | |||
| chr16:11698315 | C | T | 2 | a0011 a0017 |
2 | NA18948.hp2 NA19090.hp1 |
missense_variant | MODERATE | c.917G>A | p.Arg306Lys | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1044/3116 | 917/2877 | 306/958 | chr16 | 11698315 | |||
| chr16:11700546 | C | T | 1 | a0012 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.812G>A | p.Arg271Gln | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/12 | 939/3116 | 812/2877 | 271/958 | chr16 | 11700546 | |||
| chr16:11721634 | G | T | 1 | a0010 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.736C>A | p.Pro246Thr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/12 | 863/3116 | 736/2877 | 246/958 | chr16 | 11721634 | |||
| chr16:11730653 | T | C | 1 | a0015 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.691A>G | p.Asn231Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/12 | 818/3116 | 691/2877 | 231/958 | chr16 | 11730653 | |||
| chr16:11730713 | G | A | 1 | a0013 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.631C>T | p.Arg211Trp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/12 | 758/3116 | 631/2877 | 211/958 | chr16 | 11730713 | |||
| chr16:11736030 | C | T | 1 | a0008 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.458G>A | p.Arg153Gln | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/12 | 585/3116 | 458/2877 | 153/958 | chr16 | 11736030 | |||
| chr16:11742493 | G | C | 1 | a0006 | 3 | HG02615.hp2 HG03041.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.238C>G | p.Leu80Val | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 365/3116 | 238/2877 | 80/958 | chr16 | 11742493 | |||
| chr16:11742630 | C | G | 1 | a0016 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.101G>C | p.Ser34Thr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 228/3116 | 101/2877 | 34/958 | chr16 | 11742630 | |||
| chr16:11742652 | G | A | 4 | a0003 a0004 a0010 others(1): Show |
91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
missense_variant | MODERATE | c.79C>T | p.Pro27Ser | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 206/3116 | 79/2877 | 27/958 | chr16 | 11742652 | |||
| chr16:11742714 | C | T | 1 | a0009 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.17G>A | p.Gly6Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 144/3116 | 17/2877 | 6/958 | chr16 | 11742714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:11679405 | G | C | 2 | a0002c0011 a0002c0023 |
3 | HG02055.hp2 HG03540.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.2667C>G | p.Thr889Thr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 2794/3116 | 2667/2877 | 889/958 | chr16 | 11679405 | |||
| chr16:11687934 | G | A | 1 | a0001c0014 | 2 | HG02622.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.2076C>T | p.Cys692Cys | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/12 | 2203/3116 | 2076/2877 | 692/958 | chr16 | 11687934 | |||
| chr16:11687946 | G | A | 1 | a0001c0007 | 4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
synonymous_variant | LOW | c.2064C>T | p.Tyr688Tyr | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/12 | 2191/3116 | 2064/2877 | 688/958 | chr16 | 11687946 | |||
| chr16:11691771 | A | G | 1 | a0001c0008 | 3 | HG02165.hp1 NA18986.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.1419T>C | p.Asp473Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/12 | 1546/3116 | 1419/2877 | 473/958 | chr16 | 11691771 | |||
| chr16:11691870 | G | A | 1 | a0001c0017 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1320C>T | p.Asn440Asn | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/12 | 1447/3116 | 1320/2877 | 440/958 | chr16 | 11691870 | |||
| chr16:11692047 | A | G | 1 | a0002c0012 | 2 | NA18951.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.1143T>C | p.His381His | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/12 | 1270/3116 | 1143/2877 | 381/958 | chr16 | 11692047 | |||
| chr16:11698128 | G | A | 1 | a0001c0018 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1104C>T | p.Asp368Asp | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1231/3116 | 1104/2877 | 368/958 | chr16 | 11698128 | |||
| chr16:11698154 | G | A | 1 | a0001c0024 | 1 | NA19075.hp2 | synonymous_variant | LOW | c.1078C>T | p.Leu360Leu | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1205/3116 | 1078/2877 | 360/958 | chr16 | 11698154 | |||
| chr16:11698269 | T | C | 1 | a0001c0025 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.963A>G | p.Leu321Leu | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/12 | 1090/3116 | 963/2877 | 321/958 | chr16 | 11698269 | |||
| chr16:11742542 | C | G | 10 | a0001c0004 a0001c0007 a0001c0017 others(7): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
synonymous_variant | LOW | c.189G>C | p.Pro63Pro | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/12 | 316/3116 | 189/2877 | 63/958 | chr16 | 11742542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:11679131 | A | T | 1 | a0003c0002t0003 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 64 | chr16 | 11679131 | ||||||
| chr16:11679191 | A | C | 1 | a0002c0003t0002 | 4 | NA19058.hp1 NA19080.hp1 NA19081.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 12/12 | 4 | chr16 | 11679191 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:11679877 | C | G | 41 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
46 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2235-40G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679877 | |||||||
| chr16:11679887 | G | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(160): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2235-50C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679887 | |||||||
| chr16:11679944 | C | T | 1 | a0001c0017t0001g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2235-107G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679944 | |||||||
| chr16:11679945 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
8 | HG02074.hp1 NA18961.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.2235-108C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679945 | |||||||
| chr16:11679950 | G | A | 19 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(16): Show |
20 | HG01261.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.2235-113C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11679950 | |||||||
| chr16:11680029 | T | A | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2235-192A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680029 | |||||||
| chr16:11680125 | A | G | 25 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(22): Show |
29 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.2235-288T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680125 | |||||||
| chr16:11680345 | G | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
74 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.2235-508C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680345 | |||||||
| chr16:11680503 | G | C | 1 | a0003c0002t0003g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2235-666C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680503 | |||||||
| chr16:11680527 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2235-690C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680527 | |||||||
| chr16:11680724 | C | G | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2235-887G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680724 | |||||||
| chr16:11680769 | C | T | 97 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(94): Show |
110 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2235-932G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680769 | |||||||
| chr16:11680773 | C | T | 1 | a0003c0002t0001g0295 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2235-936G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680773 | |||||||
| chr16:11680774 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
9 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2235-937C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680774 | |||||||
| chr16:11680920 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2235-1083C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680920 | |||||||
| chr16:11680975 | T | C | 1 | a0003c0002t0001g0024 | 2 | NA18955.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2235-1138A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11680975 | |||||||
| chr16:11681019 | A | C | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2235-1182T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681019 | |||||||
| chr16:11681094 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(109): Show |
127 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2235-1257A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681094 | |||||||
| chr16:11681203 | C | G | 1 | a0003c0002t0001g0336 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2235-1366G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681203 | |||||||
| chr16:11681344 | C | G | 1 | a0002c0005t0001g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2235-1507G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681344 | |||||||
| chr16:11681388 | G | A | 1 | a0003c0002t0001g0314 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2235-1551C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681388 | |||||||
| chr16:11681644 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2235-1807G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681644 | |||||||
| chr16:11681964 | A | G | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2235-2127T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11681964 | |||||||
| chr16:11682016 | T | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2234+2149A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682016 | |||||||
| chr16:11682651 | C | T | 1 | a0003c0002t0001g0306 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2234+1514G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682651 | |||||||
| chr16:11682652 | G | A | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2234+1513C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682652 | |||||||
| chr16:11682969 | A | G | 10 | a0002c0003t0001g0144 a0002c0003t0001g0158 a0002c0003t0001g0161 others(7): Show |
10 | HG02132.hp1 HG02155.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.2234+1196T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682969 | |||||||
| chr16:11682982 | A | C | 1 | a0003c0002t0001g0024 | 2 | NA18955.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2234+1183T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682982 | |||||||
| chr16:11682983 | C | T | 1 | a0002c0003t0001g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2234+1182G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11682983 | |||||||
| chr16:11683107 | G | C | 2 | a0001c0014t0001g0073 a0001c0014t0001g0120 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2234+1058C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683107 | |||||||
| chr16:11683169 | C | A | 1 | a0001c0018t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2234+996G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683169 | |||||||
| chr16:11683196 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2234+969G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683196 | |||||||
| chr16:11683254 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2234+911C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683254 | |||||||
| chr16:11683368 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
9 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2234+797G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683368 | |||||||
| chr16:11683523 | T | C | 1 | a0002c0003t0001g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2234+642A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683523 | |||||||
| chr16:11683571 | CAGA | C | 98 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(95): Show |
111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2234+591_2234+593d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683571 | |||||||
| chr16:11683596 | T | A | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2234+569A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683596 | |||||||
| chr16:11683639 | C | T | 1 | a0002c0003t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2234+526G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683639 | |||||||
| chr16:11683649 | C | G | 2 | a0011c0021t0001g0155 a0017c0029t0001g0331 |
2 | NA18948.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2234+516G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683649 | |||||||
| chr16:11683748 | C | CT | 31 | a0001c0001t0001g0118 a0002c0003t0001g0131 a0002c0003t0001g0132 others(28): Show |
32 | HG01192.hp1 HG01261.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.2234+416dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683748 | |||||||
| chr16:11683748 | CT | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(159): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2234+416delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683748 | |||||||
| chr16:11683782 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0128 |
4 | HG01167.hp2 HG01169.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2234+383G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683782 | |||||||
| chr16:11683826 | A | C | 1 | a0002c0003t0001g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2234+339T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11683826 | |||||||
| chr16:11684069 | G | A | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2234+96C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 11/11 | chr16 | 11684069 | |||||||
| chr16:11684371 | T | A | 1 | a0003c0002t0001g0290 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2154-126A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684371 | |||||||
| chr16:11684515 | G | A | 2 | a0003c0002t0001g0303 a0003c0002t0001g0304 |
2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2154-270C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684515 | |||||||
| chr16:11684669 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2154-424T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684669 | |||||||
| chr16:11684671 | CA | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2154-427delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684671 | |||||||
| chr16:11684778 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
11 | NA18940.hp1 NA18942.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.2154-533C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684778 | |||||||
| chr16:11684836 | C | T | 1 | a0001c0004t0001g0047 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2154-591G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684836 | |||||||
| chr16:11684982 | G | A | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2154-737C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11684982 | |||||||
| chr16:11685015 | G | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0211 a0001c0001t0001g0227 others(1): Show |
5 | HG01074.hp1 HG01346.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2154-770C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685015 | |||||||
| chr16:11685207 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2154-962A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685207 | |||||||
| chr16:11685304 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2154-1059A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685304 | |||||||
| chr16:11685324 | C | T | 2 | a0001c0014t0001g0073 a0001c0014t0001g0120 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2154-1079G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685324 | |||||||
| chr16:11685334 | G | C | 1 | a0003c0002t0001g0315 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2154-1089C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685334 | |||||||
| chr16:11685385 | T | C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
63 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2154-1140A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685385 | |||||||
| chr16:11685392 | T | A | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2154-1147A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685392 | |||||||
| chr16:11685425 | C | T | 1 | a0003c0002t0001g0338 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2154-1180G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685425 | |||||||
| chr16:11685462 | G | A | 92 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
104 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.2154-1217C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685462 | |||||||
| chr16:11685469 | C | T | 41 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
46 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.2154-1224G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685469 | |||||||
| chr16:11685475 | C | A | 21 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(18): Show |
25 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.2154-1230G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685475 | |||||||
| chr16:11685581 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2154-1336C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685581 | |||||||
| chr16:11685653 | A | C | 98 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(95): Show |
111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2154-1408T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685653 | |||||||
| chr16:11685715 | C | T | 2 | a0001c0014t0001g0073 a0001c0014t0001g0120 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2154-1470G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685715 | |||||||
| chr16:11685717 | A | C | 1 | a0001c0001t0001g0223 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2154-1472T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685717 | |||||||
| chr16:11685873 | T | C | 1 | a0003c0002t0001g0325 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2154-1628A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685873 | |||||||
| chr16:11685913 | A | C | 1 | a0002c0003t0001g0186 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2154-1668T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685913 | |||||||
| chr16:11685953 | C | G | 6 | a0002c0003t0001g0143 a0002c0003t0001g0148 a0002c0003t0001g0152 others(3): Show |
6 | HG01099.hp2 HG01192.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-1708G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11685953 | |||||||
| chr16:11686075 | C | T | 1 | a0003c0002t0001g0279 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2153+1782G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686075 | |||||||
| chr16:11686654 | A | G | 2 | a0001c0001t0001g0154 a0004c0006t0001g0285 |
2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2153+1203T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686654 | |||||||
| chr16:11686690 | T | G | 1 | a0007c0013t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2153+1167A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686690 | |||||||
| chr16:11686773 | G | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(166): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.2153+1084C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686773 | |||||||
| chr16:11686799 | T | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+1058A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686799 | |||||||
| chr16:11686806 | C | G | 1 | a0002c0003t0001g0132 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2153+1051G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686806 | |||||||
| chr16:11686812 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2153+1045C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686812 | |||||||
| chr16:11686818 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+1039T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686818 | |||||||
| chr16:11686859 | T | C | 3 | a0002c0011t0001g0067 a0002c0011t0001g0068 a0002c0023t0001g0084 |
3 | HG02055.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2153+998A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686859 | |||||||
| chr16:11686918 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(169): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.2153+939A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686918 | |||||||
| chr16:11686957 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0105 a0001c0001t0001g0107 others(1): Show |
5 | HG00609.hp2 HG02135.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2153+900C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686957 | |||||||
| chr16:11686983 | G | A | 6 | a0001c0001t0001g0229 a0001c0001t0001g0234 a0001c0001t0001g0248 others(3): Show |
6 | HG00609.hp1 HG02083.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2153+874C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11686983 | |||||||
| chr16:11687024 | G | C | 1 | a0003c0002t0001g0315 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2153+833C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687024 | |||||||
| chr16:11687103 | C | G | 3 | a0002c0003t0001g0144 a0002c0003t0001g0171 a0002c0003t0001g0172 |
3 | NA18990.hp2 NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2153+754G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687103 | |||||||
| chr16:11687356 | CCTT | C | 59 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(56): Show |
65 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.2153+498_2153+500d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687356 | |||||||
| chr16:11687395 | C | A | 2 | a0001c0014t0001g0073 a0001c0014t0001g0120 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2153+462G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687395 | |||||||
| chr16:11687404 | G | A | 98 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(95): Show |
111 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.2153+453C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687404 | |||||||
| chr16:11687444 | A | G | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2153+413T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687444 | |||||||
| chr16:11687505 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+352G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687505 | |||||||
| chr16:11687598 | C | T | 2 | a0001c0014t0001g0073 a0001c0014t0001g0120 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2153+259G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687598 | |||||||
| chr16:11687726 | A | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.2153+131T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687726 | |||||||
| chr16:11687759 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(9): Show |
14 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2153+98A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687759 | |||||||
| chr16:11687835 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2153+22C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687835 | |||||||
| chr16:11687839 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(7): Show |
11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2153+18G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 10/11 | chr16 | 11687839 | |||||||
| chr16:11688162 | A | C | 1 | a0002c0003t0001g0188 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2043+141T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 9/11 | chr16 | 11688162 | |||||||
| chr16:11688193 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(10): Show |
15 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2043+110C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 9/11 | chr16 | 11688193 | |||||||
| chr16:11688468 | A | T | 1 | a0003c0002t0001g0308 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1901-23T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688468 | |||||||
| chr16:11688501 | G | A | 1 | a0011c0021t0001g0155 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1901-56C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688501 | |||||||
| chr16:11688671 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1901-226T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688671 | |||||||
| chr16:11688729 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1901-284A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688729 | |||||||
| chr16:11688799 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0111 |
2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1901-354G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688799 | |||||||
| chr16:11688944 | G | A | 5 | a0002c0003t0001g0004 a0002c0003t0001g0146 a0002c0003t0001g0150 others(2): Show |
7 | NA18939.hp2 NA18959.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1901-499C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11688944 | |||||||
| chr16:11689075 | A | T | 2 | a0002c0005t0001g0009 a0002c0005t0001g0041 |
3 | HG02886.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1901-630T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689075 | |||||||
| chr16:11689087 | C | CT | 10 | a0001c0001t0001g0225 a0002c0003t0001g0131 a0002c0003t0001g0132 others(7): Show |
10 | HG02055.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1901-643dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | |||||||
| chr16:11689087 | C | CTT | 87 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(84): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1901-644_1901-643d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | |||||||
| chr16:11689087 | C | CTTT | 11 | a0001c0001t0001g0125 a0001c0001t0001g0210 a0001c0001t0001g0212 others(8): Show |
11 | HG01175.hp2 HG02165.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1901-645_1901-643d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | |||||||
| chr16:11689087 | C | CTTTT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0001t0001g0112 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1901-646_1901-643d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | |||||||
| chr16:11689087 | C | CTTTTT | 50 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(47): Show |
56 | HG00609.hp2 HG00741.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1901-647_1901-643d others(7): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | |||||||
| chr16:11689087 | C | CTTTTTT | 6 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0001g0265 others(3): Show |
6 | HG00733.hp1 HG02145.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1901-648_1901-643d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689087 | |||||||
| chr16:11689104 | A | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1901-659T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689104 | |||||||
| chr16:11689206 | A | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
74 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1901-761T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689206 | |||||||
| chr16:11689234 | G | A | 2 | a0011c0021t0001g0155 a0017c0029t0001g0331 |
2 | NA18948.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1901-789C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689234 | |||||||
| chr16:11689242 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
74 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1901-797A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689242 | |||||||
| chr16:11689260 | T | C | 1 | a0002c0003t0001g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1901-815A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689260 | |||||||
| chr16:11689372 | T | C | 1 | a0003c0002t0001g0316 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1901-927A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689372 | |||||||
| chr16:11689467 | A | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
74 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1901-1022T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689467 | |||||||
| chr16:11689471 | T | C | 2 | a0003c0002t0001g0319 a0003c0002t0001g0320 |
2 | HG00673.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1901-1026A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689471 | |||||||
| chr16:11689616 | A | G | 1 | a0001c0014t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1901-1171T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689616 | |||||||
| chr16:11689746 | T | C | 1 | a0003c0002t0001g0326 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1901-1301A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689746 | |||||||
| chr16:11689767 | C | T | 2 | a0001c0001t0001g0154 a0004c0006t0001g0285 |
2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1901-1322G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689767 | |||||||
| chr16:11689794 | A | T | 2 | a0001c0014t0001g0073 a0001c0014t0001g0120 |
2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1901-1349T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689794 | |||||||
| chr16:11689868 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1422T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689868 | |||||||
| chr16:11689880 | C | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1410G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689880 | |||||||
| chr16:11689881 | G | A | 1 | a0002c0003t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1900+1409C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689881 | |||||||
| chr16:11689907 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1383T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689907 | |||||||
| chr16:11689908 | C | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1382G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689908 | |||||||
| chr16:11689913 | C | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1377G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689913 | |||||||
| chr16:11689925 | T | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1365A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689925 | |||||||
| chr16:11689926 | T | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1364A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689926 | |||||||
| chr16:11689928 | C | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1362G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689928 | |||||||
| chr16:11689929 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1361T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689929 | |||||||
| chr16:11689930 | C | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1360G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689930 | |||||||
| chr16:11689935 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1355T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689935 | |||||||
| chr16:11689940 | C | A | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1350G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689940 | |||||||
| chr16:11689948 | T | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1342A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689948 | |||||||
| chr16:11689949 | T | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1341A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689949 | |||||||
| chr16:11689950 | T | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1340A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689950 | |||||||
| chr16:11689960 | A | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1330T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689960 | |||||||
| chr16:11689970 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1320T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689970 | |||||||
| chr16:11689972 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1318T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689972 | |||||||
| chr16:11689975 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1315T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689975 | |||||||
| chr16:11689976 | A | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1314T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689976 | |||||||
| chr16:11689978 | C | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1312G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689978 | |||||||
| chr16:11689983 | T | A | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1307A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689983 | |||||||
| chr16:11689986 | A | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1304T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689986 | |||||||
| chr16:11689987 | C | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1303G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689987 | |||||||
| chr16:11689988 | A | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1302T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689988 | |||||||
| chr16:11689994 | C | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1296G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11689994 | |||||||
| chr16:11690025 | A | C | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1265T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690025 | |||||||
| chr16:11690065 | C | A | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1225G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690065 | |||||||
| chr16:11690067 | T | G | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1223A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690067 | |||||||
| chr16:11690082 | A | C | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1900+1208T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690082 | |||||||
| chr16:11690090 | G | A | 1 | a0001c0014t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1900+1200C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690090 | |||||||
| chr16:11690177 | C | T | 1 | a0003c0002t0001g0329 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1900+1113G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690177 | |||||||
| chr16:11690187 | C | A | 1 | a0003c0002t0001g0336 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1900+1103G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690187 | |||||||
| chr16:11690189 | A | T | 1 | a0003c0002t0001g0336 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1900+1101T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690189 | |||||||
| chr16:11690213 | T | C | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1900+1077A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690213 | |||||||
| chr16:11690273 | G | T | 164 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(161): Show |
185 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1900+1017C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690273 | |||||||
| chr16:11690473 | A | T | 19 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(16): Show |
20 | HG01261.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1900+817T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690473 | |||||||
| chr16:11690498 | A | G | 3 | a0002c0011t0001g0067 a0002c0011t0001g0068 a0002c0023t0001g0084 |
3 | HG02055.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1900+792T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690498 | |||||||
| chr16:11690610 | G | T | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(52): Show |
61 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1900+680C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690610 | |||||||
| chr16:11690661 | T | G | 1 | a0003c0002t0001g0295 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1900+629A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690661 | |||||||
| chr16:11690708 | G | A | 1 | a0001c0018t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1900+582C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690708 | |||||||
| chr16:11690719 | A | AT | 5 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(2): Show |
6 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1900+570dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690719 | |||||||
| chr16:11690821 | A | G | 1 | a0001c0004t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1900+469T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11690821 | |||||||
| chr16:11691011 | T | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 |
3 | HG03654.hp2 HG03688.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1900+279A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691011 | |||||||
| chr16:11691024 | G | A | 96 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.1900+266C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691024 | |||||||
| chr16:11691081 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0111 |
2 | NA18984.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1900+209T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691081 | |||||||
| chr16:11691109 | C | T | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(52): Show |
61 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1900+181G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 8/11 | chr16 | 11691109 | |||||||
| chr16:11692233 | G | A | 1 | a0002c0005t0001g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1108-151C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692233 | |||||||
| chr16:11692241 | T | TA | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1108-160dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692241 | |||||||
| chr16:11692548 | A | T | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
62 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1108-466T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692548 | |||||||
| chr16:11692579 | T | C | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1108-497A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692579 | |||||||
| chr16:11692611 | G | A | 1 | a0001c0004t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1108-529C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692611 | |||||||
| chr16:11692691 | C | T | 2 | a0003c0002t0001g0300 a0003c0002t0001g0302 |
2 | NA18941.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1108-609G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692691 | |||||||
| chr16:11692697 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(127): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1108-615T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692697 | |||||||
| chr16:11692766 | C | G | 2 | a0001c0001t0001g0154 a0004c0006t0001g0285 |
2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1108-684G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692766 | |||||||
| chr16:11692766 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0211 a0001c0001t0001g0227 others(1): Show |
5 | HG01074.hp1 HG01346.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108-684G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692766 | |||||||
| chr16:11692911 | G | A | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-829C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11692911 | |||||||
| chr16:11693153 | A | G | 1 | a0001c0004t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1108-1071T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693153 | |||||||
| chr16:11693200 | A | G | 3 | a0002c0003t0001g0140 a0002c0003t0001g0186 a0002c0003t0001g0188 |
3 | HG01109.hp1 HG03017.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1108-1118T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693200 | |||||||
| chr16:11693308 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1108-1226G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693308 | |||||||
| chr16:11693463 | G | A | 1 | a0003c0002t0001g0295 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1108-1381C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693463 | |||||||
| chr16:11693568 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0227 |
2 | HG01346.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1108-1486G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693568 | |||||||
| chr16:11693685 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1108-1603T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693685 | |||||||
| chr16:11693833 | C | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(92): Show |
107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1108-1751G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693833 | |||||||
| chr16:11693858 | G | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(175): Show |
199 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1108-1776C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693858 | |||||||
| chr16:11693892 | C | G | 1 | a0003c0002t0001g0295 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1108-1810G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11693892 | |||||||
| chr16:11694051 | G | A | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1108-1969C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694051 | |||||||
| chr16:11694097 | C | CT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0114 others(51): Show |
57 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1108-2016dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | C | CTT | 10 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0126 others(7): Show |
11 | HG01167.hp2 HG01175.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1108-2017_1108-201 others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | CT | C | 7 | a0002c0003t0001g0164 a0002c0003t0001g0193 a0002c0003t0001g0197 others(4): Show |
7 | HG01070.hp1 HG01168.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-2016delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | CTTTTTTT | C | 7 | a0001c0001t0001g0222 a0001c0001t0001g0229 a0001c0001t0001g0231 others(4): Show |
7 | HG02027.hp1 NA18522.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-2022_1108-201 others(11): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | CTTTTTTT others(1): Show |
C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(80): Show |
93 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1108-2023_1108-201 others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1108-2025_1108-201 others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | CTTTTTTT others(4): Show |
C | 38 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(35): Show |
43 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1108-2026_1108-201 others(15): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(12): Show |
16 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1108-2027_1108-201 others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694097 | CTTTTTTT others(7): Show |
C | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1108-2029_1108-201 others(18): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694097 | |||||||
| chr16:11694234 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1108-2152G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694234 | |||||||
| chr16:11694236 | G | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(145): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1108-2154C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694236 | |||||||
| chr16:11694434 | C | T | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1108-2352G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694434 | |||||||
| chr16:11694575 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(92): Show |
107 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1108-2493C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694575 | |||||||
| chr16:11694593 | G | A | 52 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(49): Show |
58 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1108-2511C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694593 | |||||||
| chr16:11694732 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1108-2650G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694732 | |||||||
| chr16:11694733 | G | A | 1 | a0001c0008t0001g0221 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1108-2651C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694733 | |||||||
| chr16:11694735 | G | A | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1108-2653C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694735 | |||||||
| chr16:11694832 | A | T | 1 | a0003c0002t0001g0338 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1108-2750T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694832 | |||||||
| chr16:11694854 | C | CAACTT | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1108-2773_1108-277 others(9): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11694854 | |||||||
| chr16:11695038 | T | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(7): Show |
11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108-2956A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695038 | |||||||
| chr16:11695056 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(62): Show |
73 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1108-2974C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695056 | |||||||
| chr16:11695234 | T | C | 1 | a0003c0002t0001g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1107+2891A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695234 | |||||||
| chr16:11695334 | C | T | 149 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(146): Show |
168 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1107+2791G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695334 | |||||||
| chr16:11695464 | AGT | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1107+2659_1107+266 others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695464 | |||||||
| chr16:11695519 | T | C | 25 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(22): Show |
29 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.1107+2606A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695519 | |||||||
| chr16:11695616 | C | T | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1107+2509G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695616 | |||||||
| chr16:11695715 | T | C | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(52): Show |
61 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1107+2410A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695715 | |||||||
| chr16:11695733 | G | T | 2 | a0001c0001t0001g0154 a0004c0006t0001g0285 |
2 | NA18975.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1107+2392C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11695733 | |||||||
| chr16:11696025 | C | CA | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1107+2099dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696025 | |||||||
| chr16:11696081 | C | G | 1 | a0002c0003t0001g0153 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1107+2044G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696081 | |||||||
| chr16:11696086 | G | A | 1 | a0003c0002t0001g0323 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1107+2039C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696086 | |||||||
| chr16:11696138 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1107+1987C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696138 | |||||||
| chr16:11696224 | G | C | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
62 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1107+1901C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696224 | |||||||
| chr16:11696491 | T | G | 56 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
62 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1107+1634A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696491 | |||||||
| chr16:11696614 | C | A | 1 | a0001c0007t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1107+1511G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696614 | |||||||
| chr16:11696693 | A | G | 1 | a0002c0003t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1107+1432T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696693 | |||||||
| chr16:11696805 | C | T | 1 | a0003c0002t0001g0273 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1107+1320G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11696805 | |||||||
| chr16:11697201 | A | T | 101 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(98): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1107+924T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697201 | |||||||
| chr16:11697229 | A | C | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1107+896T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697229 | |||||||
| chr16:11697241 | C | G | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0215 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107+884G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697241 | |||||||
| chr16:11697262 | C | T | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
60 | HG00609.hp2 HG00733.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1107+863G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697262 | |||||||
| chr16:11697316 | C | A | 2 | a0001c0004t0001g0049 a0001c0004t0001g0052 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1107+809G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697316 | |||||||
| chr16:11697431 | G | C | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107+694C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697431 | |||||||
| chr16:11697466 | G | A | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1107+659C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697466 | |||||||
| chr16:11697575 | A | G | 1 | a0001c0004t0001g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1107+550T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697575 | |||||||
| chr16:11697680 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(7): Show |
11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1107+445G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697680 | |||||||
| chr16:11697855 | G | T | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1107+270C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697855 | |||||||
| chr16:11697974 | T | C | 19 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(16): Show |
20 | HG01261.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1107+151A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11697974 | |||||||
| chr16:11698016 | G | C | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0215 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107+109C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11698016 | |||||||
| chr16:11698028 | A | G | 2 | a0002c0005t0001g0033 a0002c0005t0001g0038 |
2 | HG01261.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1107+97T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 7/11 | chr16 | 11698028 | |||||||
| chr16:11698438 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.907-113C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698438 | |||||||
| chr16:11698480 | C | T | 1 | a0002c0003t0001g0254 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.907-155G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698480 | |||||||
| chr16:11698595 | A | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0114 others(1): Show |
4 | HG00099.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-270T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698595 | |||||||
| chr16:11698598 | C | T | 1 | a0003c0002t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.907-273G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698598 | |||||||
| chr16:11698658 | C | G | 42 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
47 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.907-333G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698658 | |||||||
| chr16:11698717 | C | G | 1 | a0001c0014t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.907-392G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698717 | |||||||
| chr16:11698741 | T | C | 1 | a0002c0003t0001g0169 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.907-416A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698741 | |||||||
| chr16:11698798 | T | C | 1 | a0002c0003t0001g0149 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.907-473A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698798 | |||||||
| chr16:11698839 | C | T | 1 | a0001c0004t0001g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.907-514G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698839 | |||||||
| chr16:11698844 | A | C | 101 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(98): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.907-519T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698844 | |||||||
| chr16:11698942 | G | C | 1 | a0003c0002t0001g0335 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.907-617C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11698942 | |||||||
| chr16:11699053 | A | C | 2 | a0002c0005t0001g0033 a0002c0005t0001g0038 |
2 | HG01261.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.907-728T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699053 | |||||||
| chr16:11699232 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.907-907A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699232 | |||||||
| chr16:11699247 | G | GT | 176 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
196 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.907-923_907-922ins others(1): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699247 | |||||||
| chr16:11699374 | T | C | 20 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(17): Show |
21 | HG01261.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.907-1049A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699374 | |||||||
| chr16:11699440 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.906+1012C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699440 | |||||||
| chr16:11699490 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(7): Show |
11 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.906+962C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699490 | |||||||
| chr16:11699539 | C | T | 162 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(159): Show |
181 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.906+913G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699539 | |||||||
| chr16:11699843 | A | C | 20 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(17): Show |
21 | HG01261.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.906+609T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699843 | |||||||
| chr16:11699962 | A | T | 1 | a0002c0003t0001g0195 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.906+490T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699962 | |||||||
| chr16:11699969 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.906+483G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11699969 | |||||||
| chr16:11700152 | C | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+300G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700152 | |||||||
| chr16:11700211 | A | G | 57 | a0001c0001t0001g0013 a0001c0004t0001g0046 a0001c0004t0001g0051 others(54): Show |
69 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.906+241T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700211 | |||||||
| chr16:11700264 | A | T | 1 | a0003c0002t0001g0336 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.906+188T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700264 | |||||||
| chr16:11700289 | T | C | 1 | a0002c0003t0001g0176 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.906+163A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700289 | |||||||
| chr16:11700337 | A | G | 1 | a0002c0003t0002g0070 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.906+115T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 6/11 | chr16 | 11700337 | |||||||
| chr16:11700692 | G | C | 4 | a0001c0001t0001g0154 a0001c0004t0001g0049 a0001c0004t0001g0052 others(1): Show |
4 | HG03834.hp2 HG04228.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-128C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11700692 | |||||||
| chr16:11700984 | T | C | 3 | a0001c0001t0001g0265 a0007c0013t0001g0115 a0007c0013t0001g0116 |
3 | HG02145.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-420A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11700984 | |||||||
| chr16:11701038 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.794-474G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701038 | |||||||
| chr16:11701039 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.794-475G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701039 | |||||||
| chr16:11701097 | TTTA | T | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0215 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-536_794-534del others(3): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701097 | |||||||
| chr16:11701128 | C | CT | 32 | a0001c0001t0001g0011 a0001c0001t0001g0083 a0001c0001t0001g0098 others(29): Show |
33 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.794-565dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | |||||||
| chr16:11701128 | CT | C | 20 | a0001c0001t0001g0094 a0001c0001t0001g0119 a0001c0001t0001g0185 others(17): Show |
20 | HG00323.hp1 HG01070.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.794-565delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | |||||||
| chr16:11701128 | CTTT | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(13): Show |
18 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-567_794-565del others(3): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | |||||||
| chr16:11701128 | CTTTTTTT others(4): Show |
C | 6 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(3): Show |
6 | HG02056.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-575_794-565del others(11): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701128 | |||||||
| chr16:11701167 | C | T | 1 | a0002c0003t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.794-603G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701167 | |||||||
| chr16:11701168 | G | A | 1 | a0003c0002t0001g0301 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.794-604C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701168 | |||||||
| chr16:11701267 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.794-703C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701267 | |||||||
| chr16:11701285 | T | C | 4 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0002c0011t0001g0067 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-721A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701285 | |||||||
| chr16:11701357 | G | A | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-793C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701357 | |||||||
| chr16:11701417 | G | C | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.794-853C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701417 | |||||||
| chr16:11701723 | C | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
86 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.794-1159G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701723 | |||||||
| chr16:11701747 | C | T | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.794-1183G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701747 | |||||||
| chr16:11701806 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.794-1242C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701806 | |||||||
| chr16:11701976 | T | C | 1 | a0002c0003t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.794-1412A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11701976 | |||||||
| chr16:11702021 | C | CA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-1458dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702021 | |||||||
| chr16:11702034 | A | G | 1 | a0003c0002t0001g0312 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.794-1470T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702034 | |||||||
| chr16:11702056 | ATGTGTGT others(7): Show |
A | 1 | a0003c0002t0001g0317 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.794-1506_794-1493d others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702056 | |||||||
| chr16:11702063 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.794-1499A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702063 | |||||||
| chr16:11702066 | A | G | 21 | a0002c0003t0001g0137 a0002c0003t0001g0145 a0002c0005t0001g0009 others(18): Show |
23 | HG00280.hp1 HG00323.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.794-1502T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702066 | |||||||
| chr16:11702076 | G | A | 15 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(12): Show |
16 | HG01106.hp2 HG01261.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.794-1512C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702076 | |||||||
| chr16:11702086 | GTA | G | 13 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(10): Show |
14 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.794-1524_794-1523d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702086 | |||||||
| chr16:11702088 | A | G | 2 | a0002c0005t0001g0042 a0003c0002t0001g0299 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.794-1524T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702088 | |||||||
| chr16:11702090 | G | A | 2 | a0002c0005t0001g0042 a0003c0002t0001g0299 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.794-1526C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702090 | |||||||
| chr16:11702091 | T | C | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1527A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702091 | |||||||
| chr16:11702092 | G | A | 15 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(12): Show |
16 | HG01106.hp2 HG01261.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.794-1528C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | |||||||
| chr16:11702092 | G | GTA | 17 | a0001c0001t0001g0113 a0001c0001t0001g0250 a0001c0025t0001g0103 others(14): Show |
18 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-1530_794-1529d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | |||||||
| chr16:11702092 | G | GTATA | 3 | a0001c0014t0001g0073 a0003c0002t0001g0021 a0003c0002t0001g0338 |
4 | HG00280.hp1 HG01070.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1532_794-1529d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | |||||||
| chr16:11702092 | GTA | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(37): Show |
47 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.794-1530_794-1529d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702092 | |||||||
| chr16:11702094 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0083 |
2 | HG02145.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.794-1530T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702094 | |||||||
| chr16:11702095 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.794-1531A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702095 | |||||||
| chr16:11702096 | A | G | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1532T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702096 | |||||||
| chr16:11702097 | T | C | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-1533A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702097 | |||||||
| chr16:11702110 | A | G | 1 | a0002c0003t0001g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.794-1546T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702110 | |||||||
| chr16:11702187 | T | C | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-1623A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702187 | |||||||
| chr16:11702272 | A | C | 1 | a0002c0003t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.794-1708T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702272 | |||||||
| chr16:11702295 | G | C | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-1731C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702295 | |||||||
| chr16:11702335 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.794-1771G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702335 | |||||||
| chr16:11702394 | G | A | 1 | a0003c0002t0001g0021 | 2 | HG00280.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.794-1830C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702394 | |||||||
| chr16:11702405 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.794-1841A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702405 | |||||||
| chr16:11702497 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.794-1933C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702497 | |||||||
| chr16:11702523 | C | T | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-1959G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702523 | |||||||
| chr16:11702620 | A | C | 1 | a0006c0010t0001g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.794-2056T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702620 | |||||||
| chr16:11702688 | A | G | 1 | a0003c0002t0001g0311 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.794-2124T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702688 | |||||||
| chr16:11702695 | T | A | 3 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0018t0001g0030 |
3 | HG02622.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.794-2131A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702695 | |||||||
| chr16:11702703 | T | A | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.794-2139A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702703 | |||||||
| chr16:11702817 | C | A | 7 | a0001c0014t0001g0073 a0001c0018t0001g0030 a0002c0003t0001g0131 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2253G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702817 | |||||||
| chr16:11702901 | A | G | 1 | a0003c0002t0001g0318 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.794-2337T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702901 | |||||||
| chr16:11702932 | A | T | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-2368T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702932 | |||||||
| chr16:11702934 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(7): Show |
12 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-2370A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11702934 | |||||||
| chr16:11703012 | G | A | 28 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(25): Show |
33 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.794-2448C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703012 | |||||||
| chr16:11703016 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.794-2452G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703016 | |||||||
| chr16:11703059 | C | T | 1 | a0001c0025t0001g0103 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.794-2495G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703059 | |||||||
| chr16:11703148 | G | A | 4 | a0001c0004t0001g0010 a0001c0004t0001g0050 a0001c0004t0001g0060 others(1): Show |
5 | NA18946.hp1 NA18973.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-2584C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703148 | |||||||
| chr16:11703509 | T | TAC | 14 | a0001c0001t0001g0015 a0001c0001t0001g0230 a0001c0001t0001g0231 others(11): Show |
15 | HG01243.hp1 HG01261.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.794-2947_794-2946d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703509 | T | TACAC | 14 | a0001c0001t0001g0222 a0001c0001t0001g0237 a0001c0004t0001g0002 others(11): Show |
18 | HG00408.hp1 HG02015.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.794-2949_794-2946d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703509 | T | TACACACA others(3): Show |
1 | a0001c0004t0001g0063 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.794-2955_794-2946d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703509 | TAC | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
94 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.794-2947_794-2946d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703509 | TACAC | T | 79 | a0001c0001t0001g0154 a0001c0007t0001g0008 a0001c0007t0001g0028 others(76): Show |
94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.794-2949_794-2946d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703509 | TACACAC | T | 4 | a0002c0003t0001g0160 a0002c0011t0001g0067 a0002c0011t0001g0068 others(1): Show |
4 | HG03041.hp2 HG03540.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-2951_794-2946d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703509 | TACACACA others(7): Show |
T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0118 a0002c0003t0001g0117 |
3 | HG02257.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.794-2959_794-2946d others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703509 | TACACACA others(9): Show |
T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.794-2961_794-2946d others(18): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703509 | |||||||
| chr16:11703513 | C | CACACAT | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-2950_794-2949i others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703513 | |||||||
| chr16:11703543 | C | G | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-2979G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703543 | |||||||
| chr16:11703664 | G | C | 6 | a0001c0018t0001g0030 a0002c0003t0001g0131 a0002c0003t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-3100C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703664 | |||||||
| chr16:11703723 | G | A | 1 | a0002c0003t0001g0167 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.794-3159C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703723 | |||||||
| chr16:11703863 | G | A | 73 | a0001c0001t0001g0154 a0002c0003t0001g0137 a0002c0003t0001g0145 others(70): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.794-3299C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11703863 | |||||||
| chr16:11704014 | C | T | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-3450G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704014 | |||||||
| chr16:11704421 | A | G | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.794-3857T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704421 | |||||||
| chr16:11704504 | A | G | 2 | a0007c0013t0001g0115 a0007c0013t0001g0116 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-3940T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704504 | |||||||
| chr16:11704579 | C | A | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-4015G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704579 | |||||||
| chr16:11704579 | C | T | 7 | a0001c0014t0001g0073 a0001c0018t0001g0030 a0002c0003t0001g0131 others(4): Show |
7 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-4015G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704579 | |||||||
| chr16:11704744 | A | C | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-4180T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704744 | |||||||
| chr16:11704829 | A | G | 1 | a0003c0002t0001g0310 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-4265T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704829 | |||||||
| chr16:11704862 | G | C | 1 | a0001c0014t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.794-4298C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704862 | |||||||
| chr16:11704865 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(7): Show |
12 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-4301C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704865 | |||||||
| chr16:11704888 | C | G | 1 | a0011c0021t0001g0155 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.794-4324G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704888 | |||||||
| chr16:11704889 | G | A | 2 | a0002c0003t0001g0193 a0003c0002t0001g0276 |
2 | NA18948.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.794-4325C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704889 | |||||||
| chr16:11704902 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(166): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.794-4338G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704902 | |||||||
| chr16:11704915 | C | CT | 131 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(128): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.794-4352dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704915 | |||||||
| chr16:11704932 | C | T | 1 | a0001c0004t0001g0063 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.794-4368G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11704932 | |||||||
| chr16:11705020 | G | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(128): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.794-4456C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705020 | |||||||
| chr16:11705030 | G | A | 1 | a0002c0003t0001g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.794-4466C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705030 | |||||||
| chr16:11705035 | T | C | 2 | a0007c0013t0001g0115 a0007c0013t0001g0116 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-4471A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705035 | |||||||
| chr16:11705051 | T | C | 5 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-4487A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705051 | |||||||
| chr16:11705497 | A | AAG | 5 | a0002c0005t0001g0039 a0002c0005t0001g0040 a0002c0005t0001g0042 others(2): Show |
5 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-4935_794-4934d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705497 | |||||||
| chr16:11705511 | C | A | 74 | a0001c0001t0001g0154 a0002c0003t0001g0137 a0002c0003t0001g0145 others(71): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.794-4947G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705511 | |||||||
| chr16:11705598 | C | G | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-5034G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705598 | |||||||
| chr16:11705709 | C | T | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.794-5145G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705709 | |||||||
| chr16:11705728 | C | T | 34 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(31): Show |
37 | HG00609.hp2 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.794-5164G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705728 | |||||||
| chr16:11705775 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.794-5211C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705775 | |||||||
| chr16:11705817 | G | A | 1 | a0003c0002t0001g0297 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.794-5253C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705817 | |||||||
| chr16:11705848 | A | C | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-5284T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705848 | |||||||
| chr16:11705884 | G | A | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-5320C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11705884 | |||||||
| chr16:11706160 | G | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG03471.hp2 HG03654.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-5596C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706160 | |||||||
| chr16:11706165 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-5601G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706165 | |||||||
| chr16:11706363 | C | A | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.794-5799G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706363 | |||||||
| chr16:11706548 | A | C | 1 | a0002c0003t0001g0159 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.794-5984T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706548 | |||||||
| chr16:11706758 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.794-6194G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706758 | |||||||
| chr16:11706912 | A | C | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-6348T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706912 | |||||||
| chr16:11706940 | T | C | 1 | a0003c0002t0001g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.794-6376A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706940 | |||||||
| chr16:11706992 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(138): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.794-6428G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706992 | |||||||
| chr16:11706996 | G | C | 2 | a0007c0013t0001g0115 a0007c0013t0001g0116 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-6432C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11706996 | |||||||
| chr16:11707049 | T | G | 1 | a0003c0002t0001g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.794-6485A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707049 | |||||||
| chr16:11707060 | C | T | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-6496G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707060 | |||||||
| chr16:11707139 | G | C | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-6575C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707139 | |||||||
| chr16:11707234 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0238 |
2 | HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.794-6670G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707234 | |||||||
| chr16:11707317 | G | A | 1 | a0003c0002t0001g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.794-6753C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707317 | |||||||
| chr16:11707454 | A | AT | 142 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(139): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.794-6891dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707454 | |||||||
| chr16:11707814 | G | A | 2 | a0002c0005t0001g0035 a0002c0005t0001g0037 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.794-7250C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707814 | |||||||
| chr16:11707817 | C | A | 29 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(26): Show |
34 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.794-7253G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707817 | |||||||
| chr16:11707953 | G | A | 5 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-7389C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11707953 | |||||||
| chr16:11708023 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0128 |
4 | HG01167.hp2 HG01169.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-7459C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708023 | |||||||
| chr16:11708026 | G | T | 2 | a0007c0013t0001g0115 a0007c0013t0001g0116 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-7462C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708026 | |||||||
| chr16:11708110 | T | G | 2 | a0007c0013t0001g0115 a0007c0013t0001g0116 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794-7546A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708110 | |||||||
| chr16:11708239 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.794-7675A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708239 | |||||||
| chr16:11708396 | G | A | 1 | a0001c0017t0001g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794-7832C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708396 | |||||||
| chr16:11708397 | C | A | 1 | a0001c0017t0001g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794-7833G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708397 | |||||||
| chr16:11708597 | T | C | 1 | a0003c0002t0001g0318 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.794-8033A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708597 | |||||||
| chr16:11708870 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.794-8306T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708870 | |||||||
| chr16:11708971 | T | A | 15 | a0002c0003t0001g0182 a0002c0005t0001g0009 a0002c0005t0001g0033 others(12): Show |
16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-8407A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11708971 | |||||||
| chr16:11709130 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.794-8566A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709130 | |||||||
| chr16:11709259 | C | CTTTTTTT others(2): Show |
122 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(119): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.794-8704_794-8696d others(11): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709259 | |||||||
| chr16:11709259 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0096 a0001c0001t0001g0236 a0001c0001t0001g0246 others(2): Show |
5 | HG01358.hp1 HG02622.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-8705_794-8696d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709259 | |||||||
| chr16:11709377 | C | T | 39 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
42 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.794-8813G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709377 | |||||||
| chr16:11709414 | ATTTTTTG others(10): Show |
A | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.794-8867_794-8851d others(19): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709414 | |||||||
| chr16:11709423 | A | AT | 29 | a0001c0001t0001g0118 a0001c0001t0001g0265 a0002c0003t0001g0117 others(26): Show |
30 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.794-8860dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | A | ATTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
10 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-8862_794-8860d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | A | T | 1 | a0002c0003t0001g0137 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.794-8859T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | AT | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(15): Show |
18 | HG00544.hp2 HG00673.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-8860delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | ATT | A | 88 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(85): Show |
94 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.794-8861_794-8860d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | ATTT | A | 48 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(45): Show |
51 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.794-8862_794-8860d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | ATTTTTTT others(3): Show |
A | 24 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(21): Show |
28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.794-8869_794-8860d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | ATTTTTTT others(4): Show |
A | 1 | a0001c0017t0001g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794-8870_794-8860d others(13): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709423 | ATTTTTTT others(5): Show |
A | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-8871_794-8860d others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709423 | |||||||
| chr16:11709495 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.794-8931G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709495 | |||||||
| chr16:11709554 | C | T | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-8990G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709554 | |||||||
| chr16:11709591 | T | C | 131 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(128): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.794-9027A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709591 | |||||||
| chr16:11709637 | A | G | 1 | a0001c0025t0001g0103 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.794-9073T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709637 | |||||||
| chr16:11709682 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0105 a0001c0001t0001g0107 others(1): Show |
5 | HG00609.hp2 HG00621.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-9118C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709682 | |||||||
| chr16:11709683 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0111 others(1): Show |
4 | NA18939.hp1 NA18980.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-9119G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709683 | |||||||
| chr16:11709785 | G | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(122): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.794-9221C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11709785 | |||||||
| chr16:11710042 | C | T | 133 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.794-9478G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710042 | |||||||
| chr16:11710101 | C | T | 1 | a0002c0003t0001g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.794-9537G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710101 | |||||||
| chr16:11710126 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.794-9562C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710126 | |||||||
| chr16:11710198 | AT | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(218): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.794-9635delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710198 | |||||||
| chr16:11710336 | C | CAT | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(186): Show |
209 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.794-9773_794-9772i others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710336 | |||||||
| chr16:11710336 | C | T | 1 | a0002c0003t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.794-9772G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710336 | |||||||
| chr16:11710529 | C | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(127): Show |
142 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.794-9965G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710529 | |||||||
| chr16:11710592 | G | A | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.794-10028C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710592 | |||||||
| chr16:11710709 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.794-10145G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710709 | |||||||
| chr16:11710781 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0238 |
2 | HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.794-10217G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710781 | |||||||
| chr16:11710806 | C | T | 1 | a0002c0003t0001g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.794-10242G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710806 | |||||||
| chr16:11710873 | A | G | 15 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(12): Show |
16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.794-10309T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710873 | |||||||
| chr16:11710944 | G | A | 1 | a0002c0003t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.794-10380C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710944 | |||||||
| chr16:11710974 | A | ACAG | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.794-10413_794-1041 others(7): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710974 | |||||||
| chr16:11710992 | A | C | 1 | a0003c0002t0001g0330 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.794-10428T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11710992 | |||||||
| chr16:11711001 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.794-10437A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711001 | |||||||
| chr16:11711169 | C | CAT | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+10406_793+1040 others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711169 | |||||||
| chr16:11711176 | T | C | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+10401A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711176 | |||||||
| chr16:11711186 | T | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+10391A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711186 | |||||||
| chr16:11711716 | T | C | 15 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0074 others(12): Show |
17 | NA18942.hp1 NA18943.hp2 NA18960.hp2 others(14): Show |
intron_variant | MODIFIER | c.793+9861A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711716 | |||||||
| chr16:11711767 | A | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.793+9810T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711767 | |||||||
| chr16:11711970 | G | C | 1 | a0007c0013t0001g0116 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.793+9607C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711970 | |||||||
| chr16:11711998 | A | C | 1 | a0003c0002t0001g0006 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.793+9579T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11711998 | |||||||
| chr16:11712010 | T | C | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+9567A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712010 | |||||||
| chr16:11712022 | T | C | 2 | a0001c0004t0001g0058 a0001c0004t0001g0059 |
2 | HG03491.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.793+9555A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712022 | |||||||
| chr16:11712098 | C | T | 1 | a0010c0028t0001g0269 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.793+9479G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712098 | |||||||
| chr16:11712143 | G | C | 1 | a0002c0003t0001g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.793+9434C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712143 | |||||||
| chr16:11712156 | A | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(64): Show |
75 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.793+9421T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712156 | |||||||
| chr16:11712214 | G | A | 15 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(12): Show |
16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.793+9363C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712214 | |||||||
| chr16:11712215 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.793+9362C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712215 | |||||||
| chr16:11712649 | T | C | 1 | a0002c0003t0001g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793+8928A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712649 | |||||||
| chr16:11712858 | T | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+8719A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712858 | |||||||
| chr16:11712922 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+8655G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712922 | |||||||
| chr16:11712929 | A | AAACACAC others(6): Show |
1 | a0013c0027t0001g0264 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.793+8647_793+8648i others(15): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AAC | 106 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(103): Show |
117 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.793+8646_793+8647d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACAC | 10 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0004t0001g0032 others(7): Show |
10 | HG00741.hp2 HG02027.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+8644_793+8647d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACACAC | 20 | a0001c0001t0001g0012 a0001c0001t0001g0091 a0001c0001t0001g0092 others(17): Show |
22 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.793+8642_793+8647d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACACACA others(1): Show |
3 | a0001c0001t0001g0122 a0001c0001t0001g0207 a0002c0005t0001g0039 |
3 | HG02896.hp2 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.793+8640_793+8647d others(10): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACACACA others(3): Show |
5 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG01346.hp2 HG03471.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+8638_793+8647d others(12): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACACACA others(5): Show |
40 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(37): Show |
44 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.793+8636_793+8647d others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACACACA others(7): Show |
12 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0212 others(9): Show |
14 | HG01175.hp2 HG01496.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.793+8634_793+8647d others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACACACA others(9): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
7 | HG02165.hp1 HG03490.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.793+8632_793+8647d others(18): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | A | AACACACA others(11): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG01070.hp2 HG01071.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.793+8630_793+8647d others(20): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | AACACAC | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0245 a0001c0001t0001g0246 |
4 | HG01256.hp1 HG01358.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+8642_793+8647d others(8): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712929 | AACACACA others(5): Show |
A | 6 | a0002c0003t0001g0165 a0002c0003t0001g0167 a0002c0003t0001g0169 others(3): Show |
6 | HG00408.hp2 HG00621.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.793+8636_793+8647d others(14): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712929 | |||||||
| chr16:11712959 | G | C | 1 | a0002c0003t0002g0069 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.793+8618C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11712959 | |||||||
| chr16:11713048 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0240 |
2 | NA18980.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.793+8529C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713048 | |||||||
| chr16:11713052 | A | G | 1 | a0003c0002t0001g0292 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.793+8525T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713052 | |||||||
| chr16:11713095 | G | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+8482C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713095 | |||||||
| chr16:11713110 | G | GA | 84 | a0001c0001t0001g0154 a0001c0004t0001g0053 a0002c0003t0001g0137 others(81): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.793+8466dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | |||||||
| chr16:11713110 | G | GAA | 9 | a0003c0002t0001g0292 a0003c0002t0001g0293 a0003c0002t0001g0297 others(6): Show |
9 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+8465_793+8466d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | |||||||
| chr16:11713110 | GA | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
83 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.793+8466delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | |||||||
| chr16:11713110 | GAA | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0118 others(16): Show |
21 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.793+8465_793+8466d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | |||||||
| chr16:11713110 | GAAA | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(36): Show |
42 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.793+8464_793+8466d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | |||||||
| chr16:11713110 | GAAAA | G | 9 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(6): Show |
10 | HG01891.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+8463_793+8466d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713110 | |||||||
| chr16:11713111 | A | G | 1 | a0001c0004t0001g0055 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.793+8466T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713111 | |||||||
| chr16:11713241 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.793+8336A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713241 | |||||||
| chr16:11713280 | C | CA | 35 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(32): Show |
41 | HG00408.hp1 HG00544.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.793+8296dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713280 | |||||||
| chr16:11713280 | CA | C | 52 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(49): Show |
56 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.793+8296delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713280 | |||||||
| chr16:11713511 | G | C | 1 | a0002c0011t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.793+8066C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713511 | |||||||
| chr16:11713582 | A | C | 1 | a0001c0004t0001g0053 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.793+7995T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713582 | |||||||
| chr16:11713606 | G | A | 1 | a0001c0001t0001g0005 | 3 | NA18952.hp2 NA19004.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.793+7971C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713606 | |||||||
| chr16:11713657 | C | A | 4 | a0002c0003t0002g0069 a0002c0003t0002g0070 a0002c0003t0002g0071 others(1): Show |
4 | NA19058.hp1 NA19080.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+7920G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713657 | |||||||
| chr16:11713661 | G | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(138): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.793+7916C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713661 | |||||||
| chr16:11713773 | G | A | 1 | a0002c0011t0001g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.793+7804C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713773 | |||||||
| chr16:11713886 | G | A | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+7691C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713886 | |||||||
| chr16:11713983 | T | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0238 |
2 | HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.793+7594A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713983 | |||||||
| chr16:11713990 | T | C | 1 | a0001c0018t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+7587A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11713990 | |||||||
| chr16:11714024 | G | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0215 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+7553C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714024 | |||||||
| chr16:11714046 | A | AT | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(135): Show |
152 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.793+7530dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714046 | |||||||
| chr16:11714067 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.793+7510C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714067 | |||||||
| chr16:11714257 | C | T | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.793+7320G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714257 | |||||||
| chr16:11714287 | G | C | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.793+7290C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714287 | |||||||
| chr16:11714289 | G | T | 1 | a0002c0003t0001g0158 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.793+7288C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714289 | |||||||
| chr16:11714358 | T | G | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.793+7219A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714358 | |||||||
| chr16:11714496 | C | T | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+7081G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714496 | |||||||
| chr16:11714588 | C | T | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+6989G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714588 | |||||||
| chr16:11714611 | G | A | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.793+6966C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714611 | |||||||
| chr16:11714639 | C | CA | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+6937dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714639 | |||||||
| chr16:11714726 | A | T | 4 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0002c0011t0001g0067 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+6851T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714726 | |||||||
| chr16:11714871 | G | A | 4 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0002c0011t0001g0067 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+6706C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714871 | |||||||
| chr16:11714913 | A | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.793+6664T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714913 | |||||||
| chr16:11714950 | T | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.793+6627A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11714950 | |||||||
| chr16:11715127 | C | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0114 others(1): Show |
4 | HG00099.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+6450G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715127 | |||||||
| chr16:11715184 | G | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0114 others(1): Show |
4 | HG00099.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+6393C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715184 | |||||||
| chr16:11715200 | A | C | 1 | a0001c0007t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.793+6377T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715200 | |||||||
| chr16:11715424 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.793+6153G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715424 | |||||||
| chr16:11715462 | CA | C | 187 | a0001c0001t0001g0154 a0001c0001t0001g0234 a0001c0001t0001g0258 others(184): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.793+6114delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715462 | |||||||
| chr16:11715462 | CAA | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(122): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.793+6113_793+6114d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715462 | |||||||
| chr16:11715462 | CAAA | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+6112_793+6114d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715462 | |||||||
| chr16:11715562 | A | T | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+6015T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715562 | |||||||
| chr16:11715836 | C | T | 2 | a0003c0002t0001g0006 a0003c0002t0001g0277 |
4 | HG00099.hp1 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+5741G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715836 | |||||||
| chr16:11715865 | T | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.793+5712A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715865 | |||||||
| chr16:11715945 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.793+5632T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715945 | |||||||
| chr16:11715980 | G | A | 1 | a0002c0003t0001g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.793+5597C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11715980 | |||||||
| chr16:11716083 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.793+5494G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716083 | |||||||
| chr16:11716084 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(181): Show |
204 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.793+5493T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716084 | |||||||
| chr16:11716526 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(186): Show |
209 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.793+5051A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716526 | |||||||
| chr16:11716534 | T | C | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793+5043A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716534 | |||||||
| chr16:11716618 | A | G | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.793+4959T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11716618 | |||||||
| chr16:11717002 | G | T | 1 | a0001c0014t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793+4575C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717002 | |||||||
| chr16:11717108 | G | GA | 14 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0237 others(11): Show |
14 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.793+4468dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717108 | |||||||
| chr16:11717109 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.793+4468T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717109 | |||||||
| chr16:11717140 | A | C | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.793+4437T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717140 | |||||||
| chr16:11717190 | C | T | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+4387G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717190 | |||||||
| chr16:11717311 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(70): Show |
81 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.793+4266C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717311 | |||||||
| chr16:11717366 | C | T | 1 | a0001c0018t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+4211G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717366 | |||||||
| chr16:11717434 | G | GA | 96 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(93): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.793+4142dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717434 | |||||||
| chr16:11717434 | G | GAA | 11 | a0001c0001t0001g0118 a0001c0001t0001g0206 a0001c0001t0001g0207 others(8): Show |
11 | HG01192.hp2 HG02257.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+4141_793+4142d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717434 | |||||||
| chr16:11717434 | GA | G | 34 | a0001c0001t0001g0105 a0001c0004t0001g0002 a0001c0004t0001g0010 others(31): Show |
38 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.793+4142delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717434 | |||||||
| chr16:11717436 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.793+4141T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717436 | |||||||
| chr16:11717547 | C | T | 2 | a0004c0006t0001g0007 a0004c0006t0001g0337 |
4 | NA18940.hp1 NA18951.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.793+4030G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717547 | |||||||
| chr16:11717587 | C | T | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0215 others(2): Show |
5 | HG00280.hp2 HG01192.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+3990G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717587 | |||||||
| chr16:11717639 | G | T | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3938C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717639 | |||||||
| chr16:11717640 | TGAAACCC others(353): Show |
T | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3577_793+3936d others(2): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717640 | |||||||
| chr16:11717872 | G | C | 31 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0031 others(28): Show |
36 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.793+3705C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717872 | |||||||
| chr16:11717933 | C | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(70): Show |
81 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.793+3644G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11717933 | |||||||
| chr16:11718003 | G | A | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3574C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718003 | |||||||
| chr16:11718004 | T | C | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3573A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718004 | |||||||
| chr16:11718019 | T | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3558A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718019 | |||||||
| chr16:11718021 | T | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3556A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718021 | |||||||
| chr16:11718027 | T | A | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3550A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718027 | |||||||
| chr16:11718031 | T | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3546A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718031 | |||||||
| chr16:11718032 | A | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3545T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718032 | |||||||
| chr16:11718033 | A | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3544T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718033 | |||||||
| chr16:11718034 | A | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3543T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718034 | |||||||
| chr16:11718035 | A | G | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3542T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718035 | |||||||
| chr16:11718036 | A | T | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3541T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718036 | |||||||
| chr16:11718059 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793+3518C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718059 | |||||||
| chr16:11718164 | A | C | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3413T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718164 | |||||||
| chr16:11718165 | T | A | 2 | a0002c0003t0001g0136 a0002c0003t0001g0184 |
2 | HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+3412A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718165 | |||||||
| chr16:11718216 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0113 |
2 | HG00733.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.793+3361C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718216 | |||||||
| chr16:11718219 | T | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+3358A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718219 | |||||||
| chr16:11718271 | T | TA | 29 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(26): Show |
34 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.793+3305dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718271 | |||||||
| chr16:11718381 | T | C | 1 | a0002c0003t0001g0173 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.793+3196A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718381 | |||||||
| chr16:11718435 | C | T | 159 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(156): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.793+3142G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718435 | |||||||
| chr16:11718489 | C | CT | 8 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | NA18612.hp2 NA18955.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+3087dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718489 | |||||||
| chr16:11718602 | A | T | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.793+2975T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718602 | |||||||
| chr16:11718693 | A | T | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.793+2884T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11718693 | |||||||
| chr16:11719089 | T | C | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.793+2488A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719089 | |||||||
| chr16:11719358 | C | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0238 a0005c0009t0001g0247 |
3 | HG01496.hp1 HG01993.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.793+2219G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719358 | |||||||
| chr16:11719489 | T | C | 1 | a0003c0002t0001g0295 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.793+2088A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719489 | |||||||
| chr16:11719789 | C | T | 1 | a0005c0009t0001g0247 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.793+1788G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719789 | |||||||
| chr16:11719880 | C | T | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.793+1697G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11719880 | |||||||
| chr16:11720043 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(139): Show |
156 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.793+1534C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720043 | |||||||
| chr16:11720240 | A | G | 21 | a0002c0003t0001g0144 a0002c0003t0001g0158 a0002c0003t0001g0159 others(18): Show |
21 | HG00408.hp2 HG00621.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.793+1337T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720240 | |||||||
| chr16:11720416 | A | AT | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.793+1160dupA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720416 | |||||||
| chr16:11720416 | AT | A | 24 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(21): Show |
28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.793+1160delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720416 | |||||||
| chr16:11720515 | A | G | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+1062T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720515 | |||||||
| chr16:11720664 | G | A | 1 | a0001c0014t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793+913C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720664 | |||||||
| chr16:11720706 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(138): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.793+871G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720706 | |||||||
| chr16:11720748 | T | G | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+829A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11720748 | |||||||
| chr16:11721074 | C | T | 1 | a0002c0005t0001g0039 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.793+503G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721074 | |||||||
| chr16:11721165 | C | T | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+412G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721165 | |||||||
| chr16:11721322 | C | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(183): Show |
206 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.793+255G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721322 | |||||||
| chr16:11721362 | A | G | 1 | a0001c0018t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+215T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721362 | |||||||
| chr16:11721418 | G | A | 2 | a0001c0001t0001g0118 a0002c0003t0001g0117 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.793+159C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721418 | |||||||
| chr16:11721438 | A | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+139T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721438 | |||||||
| chr16:11721464 | C | G | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793+113G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721464 | |||||||
| chr16:11721470 | G | C | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.793+107C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721470 | |||||||
| chr16:11721476 | G | A | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.793+101C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721476 | |||||||
| chr16:11721516 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.793+61C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721516 | |||||||
| chr16:11721525 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.793+52A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 5/11 | chr16 | 11721525 | |||||||
| chr16:11721953 | G | A | 1 | a0002c0003t0001g0182 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.700-283C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11721953 | |||||||
| chr16:11722035 | G | A | 1 | a0001c0004t0001g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.700-365C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722035 | |||||||
| chr16:11722048 | C | A | 1 | a0002c0005t0001g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.700-378G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722048 | |||||||
| chr16:11722108 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-438G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722108 | |||||||
| chr16:11722209 | C | G | 1 | a0003c0002t0001g0282 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.700-539G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722209 | |||||||
| chr16:11722251 | C | G | 1 | a0002c0003t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.700-581G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722251 | |||||||
| chr16:11722399 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.700-729A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722399 | |||||||
| chr16:11722757 | T | C | 2 | a0006c0010t0001g0266 a0006c0010t0001g0267 |
2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700-1087A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722757 | |||||||
| chr16:11722815 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.700-1145C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722815 | |||||||
| chr16:11722996 | C | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-1326G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722996 | |||||||
| chr16:11722999 | G | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-1329C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11722999 | |||||||
| chr16:11723121 | G | A | 4 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0002c0011t0001g0067 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-1451C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723121 | |||||||
| chr16:11723149 | T | A | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.700-1479A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723149 | |||||||
| chr16:11723193 | G | A | 27 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(24): Show |
32 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.700-1523C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723193 | |||||||
| chr16:11723251 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.700-1581C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723251 | |||||||
| chr16:11723278 | GAAAA | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(12): Show |
17 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.700-1612_700-1609d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723278 | |||||||
| chr16:11723351 | G | T | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.700-1681C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723351 | |||||||
| chr16:11723356 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(138): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.700-1686T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723356 | |||||||
| chr16:11723372 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.700-1702C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723372 | |||||||
| chr16:11723391 | C | T | 1 | a0012c0020t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.700-1721G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723391 | |||||||
| chr16:11723517 | G | A | 2 | a0007c0013t0001g0115 a0007c0013t0001g0116 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.700-1847C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723517 | |||||||
| chr16:11723610 | A | C | 16 | a0002c0003t0001g0141 a0002c0003t0001g0198 a0002c0005t0001g0009 others(13): Show |
17 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.700-1940T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11723610 | |||||||
| chr16:11724093 | G | C | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.700-2423C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724093 | |||||||
| chr16:11724642 | T | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
9 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-2972A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724642 | |||||||
| chr16:11724698 | T | C | 6 | a0002c0003t0002g0069 a0002c0003t0002g0070 a0002c0003t0002g0071 others(3): Show |
6 | NA18951.hp2 NA19010.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.700-3028A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724698 | |||||||
| chr16:11724730 | C | G | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.700-3060G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724730 | |||||||
| chr16:11724851 | T | C | 21 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(18): Show |
25 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.700-3181A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724851 | |||||||
| chr16:11724961 | G | C | 1 | a0001c0018t0001g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.700-3291C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724961 | |||||||
| chr16:11724982 | T | C | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.700-3312A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11724982 | |||||||
| chr16:11725034 | G | A | 1 | a0002c0003t0001g0201 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.700-3364C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725034 | |||||||
| chr16:11725112 | G | A | 1 | a0003c0002t0001g0021 | 2 | HG00280.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.700-3442C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725112 | |||||||
| chr16:11725344 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.700-3674A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725344 | |||||||
| chr16:11725356 | T | C | 1 | a0002c0003t0001g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.700-3686A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725356 | |||||||
| chr16:11725358 | GA | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-3689delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725358 | |||||||
| chr16:11725392 | C | A | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.700-3722G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725392 | |||||||
| chr16:11725406 | A | T | 1 | a0002c0003t0001g0193 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.700-3736T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725406 | |||||||
| chr16:11725474 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-3804C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725474 | |||||||
| chr16:11725538 | C | T | 1 | a0002c0003t0001g0143 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.700-3868G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725538 | |||||||
| chr16:11725567 | T | C | 1 | a0003c0002t0001g0321 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.700-3897A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725567 | |||||||
| chr16:11725570 | C | T | 4 | a0002c0011t0001g0067 a0002c0011t0001g0068 a0006c0010t0001g0266 others(1): Show |
4 | HG02615.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-3900G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725570 | |||||||
| chr16:11725713 | C | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(178): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.700-4043G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725713 | |||||||
| chr16:11725796 | C | T | 1 | a0013c0027t0001g0264 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.700-4126G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725796 | |||||||
| chr16:11725904 | C | G | 1 | a0002c0003t0002g0069 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.700-4234G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11725904 | |||||||
| chr16:11726123 | T | G | 1 | a0001c0004t0001g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.700-4453A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726123 | |||||||
| chr16:11726147 | G | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.700-4477C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726147 | |||||||
| chr16:11726222 | AGC | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.699+4421_699+4422d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726222 | |||||||
| chr16:11726293 | C | T | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.699+4352G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726293 | |||||||
| chr16:11726311 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.699+4334C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726311 | |||||||
| chr16:11726364 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.699+4281G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726364 | |||||||
| chr16:11726389 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.699+4256A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726389 | |||||||
| chr16:11726400 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(137): Show |
154 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.699+4245C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726400 | |||||||
| chr16:11726550 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0089 |
2 | NA18967.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.699+4095T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726550 | |||||||
| chr16:11726567 | G | A | 1 | a0003c0002t0001g0324 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.699+4078C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726567 | |||||||
| chr16:11726579 | C | CA | 29 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0032 others(26): Show |
34 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.699+4065dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726579 | |||||||
| chr16:11726579 | CA | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(133): Show |
150 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.699+4065delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726579 | |||||||
| chr16:11726856 | A | T | 1 | a0002c0003t0001g0193 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.699+3789T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11726856 | |||||||
| chr16:11727009 | C | T | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+3636G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727009 | |||||||
| chr16:11727032 | G | A | 2 | a0003c0002t0001g0006 a0003c0002t0001g0277 |
4 | HG00099.hp1 HG01074.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+3613C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727032 | |||||||
| chr16:11727040 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG01358.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.699+3605C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727040 | |||||||
| chr16:11727072 | T | C | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.699+3573A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727072 | |||||||
| chr16:11727113 | T | A | 1 | a0003c0002t0001g0281 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.699+3532A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727113 | |||||||
| chr16:11727115 | A | T | 1 | a0003c0002t0001g0281 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.699+3530T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727115 | |||||||
| chr16:11727195 | AT | A | 24 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(21): Show |
28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.699+3449delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727195 | |||||||
| chr16:11727204 | C | T | 1 | a0003c0002t0001g0272 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.699+3441G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727204 | |||||||
| chr16:11727598 | G | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(65): Show |
76 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.699+3047C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727598 | |||||||
| chr16:11727643 | C | T | 1 | a0003c0002t0001g0305 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.699+3002G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727643 | |||||||
| chr16:11727652 | A | G | 76 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
84 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.699+2993T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727652 | |||||||
| chr16:11727662 | G | GC | 40 | a0001c0001t0001g0020 a0001c0001t0001g0080 a0001c0001t0001g0086 others(37): Show |
41 | HG00597.hp2 HG00673.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.699+2982dupG | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727662 | |||||||
| chr16:11727670 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0111 others(1): Show |
4 | NA18939.hp1 NA18980.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+2975G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727670 | |||||||
| chr16:11727788 | G | A | 52 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(49): Show |
56 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.699+2857C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727788 | |||||||
| chr16:11727852 | G | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
82 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.699+2793C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11727852 | |||||||
| chr16:11728111 | T | A | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.699+2534A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728111 | |||||||
| chr16:11728143 | A | T | 2 | a0002c0003t0001g0141 a0002c0003t0001g0198 |
2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.699+2502T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728143 | |||||||
| chr16:11728210 | T | C | 75 | a0002c0003t0001g0137 a0002c0003t0001g0173 a0002c0003t0001g0205 others(72): Show |
89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.699+2435A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728210 | |||||||
| chr16:11728292 | A | G | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.699+2353T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728292 | |||||||
| chr16:11728538 | A | C | 1 | a0002c0003t0001g0145 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.699+2107T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728538 | |||||||
| chr16:11728592 | C | A | 1 | a0002c0003t0001g0184 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.699+2053G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728592 | |||||||
| chr16:11728802 | C | G | 2 | a0003c0002t0001g0303 a0003c0002t0001g0304 |
2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.699+1843G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11728802 | |||||||
| chr16:11729000 | A | AAATC | 15 | a0002c0003t0001g0201 a0002c0005t0001g0009 a0002c0005t0001g0033 others(12): Show |
16 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.699+1641_699+1644d others(6): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729000 | |||||||
| chr16:11729464 | T | TAG | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(184): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.699+1179_699+1180d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729464 | |||||||
| chr16:11729514 | T | C | 3 | a0006c0010t0001g0266 a0006c0010t0001g0267 a0006c0010t0001g0268 |
3 | HG02615.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.699+1131A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729514 | |||||||
| chr16:11729819 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.699+826C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729819 | |||||||
| chr16:11729965 | C | T | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.699+680G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11729965 | |||||||
| chr16:11730063 | G | A | 6 | a0001c0004t0001g0046 a0001c0004t0001g0051 a0001c0004t0001g0063 others(3): Show |
6 | HG00408.hp1 HG02015.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.699+582C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730063 | |||||||
| chr16:11730139 | G | A | 1 | a0002c0003t0001g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.699+506C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730139 | |||||||
| chr16:11730196 | C | G | 6 | a0001c0014t0001g0073 a0002c0003t0001g0131 a0002c0003t0001g0132 others(3): Show |
6 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.699+449G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730196 | |||||||
| chr16:11730200 | T | G | 129 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(126): Show |
141 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.699+445A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730200 | |||||||
| chr16:11730476 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.699+169A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730476 | |||||||
| chr16:11730535 | T | C | 1 | a0002c0003t0001g0195 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.699+110A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 4/11 | chr16 | 11730535 | |||||||
| chr16:11730783 | AAAAAAT | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0113 |
3 | HG00733.hp1 HG00741.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.570-15_570-10delAT others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11730783 | |||||||
| chr16:11730842 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.570-68A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11730842 | |||||||
| chr16:11730904 | C | A | 7 | a0002c0005t0001g0009 a0002c0005t0001g0039 a0002c0005t0001g0040 others(4): Show |
8 | HG02717.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.570-130G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11730904 | |||||||
| chr16:11731047 | C | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(184): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.570-273G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731047 | |||||||
| chr16:11731256 | A | G | 55 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(52): Show |
59 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.570-482T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731256 | |||||||
| chr16:11731657 | T | G | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.570-883A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731657 | |||||||
| chr16:11731687 | T | TCA | 22 | a0001c0001t0001g0081 a0001c0001t0001g0252 a0001c0001t0001g0253 others(19): Show |
23 | HG00621.hp2 HG01106.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.570-915_570-914dup others(2): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | |||||||
| chr16:11731687 | T | TCACA | 3 | a0002c0005t0001g0043 a0002c0011t0001g0067 a0002c0011t0001g0068 |
3 | HG01891.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.570-917_570-914dup others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | |||||||
| chr16:11731687 | TCA | T | 50 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(47): Show |
53 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.570-915_570-914del others(2): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | |||||||
| chr16:11731687 | TCACACAC others(9): Show |
T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.570-929_570-914del others(16): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731687 | |||||||
| chr16:11731716 | C | T | 1 | a0002c0003t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.570-942G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11731716 | |||||||
| chr16:11732012 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.570-1238C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732012 | |||||||
| chr16:11732120 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0124 |
3 | HG03654.hp2 HG03688.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.570-1346G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732120 | |||||||
| chr16:11732157 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.570-1383G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732157 | |||||||
| chr16:11732292 | T | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(72): Show |
83 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.570-1518A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732292 | |||||||
| chr16:11732308 | C | T | 1 | a0001c0014t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.570-1534G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732308 | |||||||
| chr16:11732309 | G | A | 1 | a0002c0003t0001g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.570-1535C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732309 | |||||||
| chr16:11732399 | C | A | 6 | a0002c0003t0001g0144 a0002c0003t0001g0171 a0002c0003t0001g0172 others(3): Show |
6 | NA18941.hp1 NA18952.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+1583G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732399 | |||||||
| chr16:11732424 | G | A | 1 | a0003c0002t0001g0329 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.569+1558C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732424 | |||||||
| chr16:11732729 | G | A | 1 | a0002c0023t0001g0084 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.569+1253C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732729 | |||||||
| chr16:11732818 | G | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.569+1164C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732818 | |||||||
| chr16:11732824 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.569+1158C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732824 | |||||||
| chr16:11732985 | T | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(185): Show |
208 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.569+997A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11732985 | |||||||
| chr16:11733034 | G | A | 5 | a0002c0003t0001g0140 a0002c0003t0001g0186 a0002c0003t0001g0187 others(2): Show |
5 | HG01109.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.569+948C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733034 | |||||||
| chr16:11733149 | C | T | 1 | a0001c0007t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.569+833G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733149 | |||||||
| chr16:11733188 | G | A | 1 | a0002c0003t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.569+794C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733188 | |||||||
| chr16:11733204 | C | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(127): Show |
142 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.569+778G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733204 | |||||||
| chr16:11733296 | T | A | 1 | a0003c0002t0001g0338 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.569+686A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733296 | |||||||
| chr16:11733449 | T | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(184): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.569+533A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733449 | |||||||
| chr16:11733564 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.569+418A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733564 | |||||||
| chr16:11733674 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.569+308G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733674 | |||||||
| chr16:11733687 | G | A | 133 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(130): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.569+295C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733687 | |||||||
| chr16:11733690 | T | C | 49 | a0002c0003t0001g0173 a0002c0003t0001g0205 a0003c0002t0001g0001 others(46): Show |
62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.569+292A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 3/11 | chr16 | 11733690 | |||||||
| chr16:11734109 | C | T | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.472-30G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734109 | |||||||
| chr16:11734116 | T | C | 2 | a0001c0001t0001g0118 a0002c0003t0001g0117 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.472-37A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734116 | |||||||
| chr16:11734162 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(283): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.472-83T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734162 | |||||||
| chr16:11734209 | T | C | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-130A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734209 | |||||||
| chr16:11734287 | T | G | 1 | a0002c0003t0001g0191 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.472-208A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734287 | |||||||
| chr16:11734425 | T | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
85 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.472-346A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734425 | |||||||
| chr16:11734426 | T | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.472-347A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734426 | |||||||
| chr16:11734550 | C | A | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.472-471G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734550 | |||||||
| chr16:11734711 | G | A | 41 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
44 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.472-632C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734711 | |||||||
| chr16:11734845 | A | T | 128 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(125): Show |
140 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.472-766T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734845 | |||||||
| chr16:11734882 | A | G | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-803T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11734882 | |||||||
| chr16:11735159 | T | G | 1 | a0001c0001t0001g0255 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.471+858A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735159 | |||||||
| chr16:11735317 | C | T | 3 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 |
4 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+700G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735317 | |||||||
| chr16:11735353 | T | C | 4 | a0003c0002t0001g0330 a0004c0006t0001g0007 a0004c0006t0001g0337 others(1): Show |
6 | HG02056.hp2 NA18940.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+664A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735353 | |||||||
| chr16:11735385 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.471+632C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735385 | |||||||
| chr16:11735514 | CT | C | 5 | a0002c0003t0001g0131 a0002c0003t0001g0132 a0002c0003t0001g0133 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+502delA | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735514 | |||||||
| chr16:11735517 | G | C | 1 | a0006c0010t0001g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.471+500C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735517 | |||||||
| chr16:11735543 | G | T | 1 | a0003c0002t0001g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.471+474C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735543 | |||||||
| chr16:11735863 | C | A | 1 | a0008c0019t0001g0085 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.471+154G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 2/11 | chr16 | 11735863 | |||||||
| chr16:11736348 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.255-115A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11736348 | |||||||
| chr16:11736919 | G | A | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-686C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11736919 | |||||||
| chr16:11737082 | T | C | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.255-849A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737082 | |||||||
| chr16:11737174 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(187): Show |
210 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.255-941A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737174 | |||||||
| chr16:11737175 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.255-942C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737175 | |||||||
| chr16:11737334 | T | A | 311 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(308): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.255-1101A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737334 | |||||||
| chr16:11737400 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.255-1167C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737400 | |||||||
| chr16:11737543 | C | A | 1 | a0003c0002t0001g0278 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.255-1310G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737543 | |||||||
| chr16:11737590 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0118 a0001c0001t0001g0125 others(6): Show |
11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.255-1357C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737590 | |||||||
| chr16:11737817 | C | A | 1 | a0001c0017t0001g0048 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.255-1584G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737817 | |||||||
| chr16:11737851 | C | CA | 38 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0083 others(35): Show |
41 | HG00597.hp1 HG00597.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.255-1619dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737851 | |||||||
| chr16:11737851 | C | CAA | 19 | a0001c0001t0001g0130 a0001c0004t0001g0002 a0001c0004t0001g0010 others(16): Show |
23 | HG00408.hp1 HG00544.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.255-1620_255-1619d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737851 | |||||||
| chr16:11737851 | CA | C | 7 | a0001c0001t0001g0261 a0002c0003t0001g0143 a0002c0003t0001g0144 others(4): Show |
7 | HG00323.hp1 HG01070.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.255-1619delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11737851 | |||||||
| chr16:11738020 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.255-1787C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738020 | |||||||
| chr16:11738342 | A | G | 4 | a0003c0002t0001g0022 a0003c0002t0001g0270 a0003c0002t0001g0271 others(1): Show |
5 | NA18988.hp2 NA19003.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-2109T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738342 | |||||||
| chr16:11738353 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(101): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.255-2120T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738353 | |||||||
| chr16:11738407 | C | G | 1 | a0009c0015t0001g0026 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.255-2174G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738407 | |||||||
| chr16:11738436 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.255-2203A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738436 | |||||||
| chr16:11738445 | G | A | 1 | a0002c0003t0001g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.255-2212C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738445 | |||||||
| chr16:11738455 | T | C | 1 | a0015c0026t0001g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.255-2222A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738455 | |||||||
| chr16:11738661 | G | GAA | 25 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0047 others(22): Show |
30 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.255-2430_255-2429d others(4): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738661 | |||||||
| chr16:11738661 | G | GAAA | 19 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0066 others(16): Show |
20 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.255-2431_255-2429d others(5): Show |
TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738661 | |||||||
| chr16:11738661 | GA | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
16 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.255-2429delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738661 | |||||||
| chr16:11738712 | G | A | 2 | a0004c0006t0001g0007 a0004c0006t0001g0337 |
4 | NA18940.hp1 NA18951.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-2479C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738712 | |||||||
| chr16:11738875 | A | G | 1 | a0002c0003t0001g0142 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.255-2642T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738875 | |||||||
| chr16:11738989 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.255-2756A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11738989 | |||||||
| chr16:11739325 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.255-3092C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739325 | |||||||
| chr16:11739515 | C | T | 1 | a0003c0002t0001g0338 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.254+2962G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739515 | |||||||
| chr16:11739556 | C | G | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+2921G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739556 | |||||||
| chr16:11739600 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0125 others(5): Show |
10 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.254+2877G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739600 | |||||||
| chr16:11739606 | A | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.254+2871T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739606 | |||||||
| chr16:11739661 | T | C | 24 | a0001c0001t0001g0114 a0001c0004t0001g0002 a0001c0004t0001g0010 others(21): Show |
28 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.254+2816A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739661 | |||||||
| chr16:11739762 | C | T | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+2715G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739762 | |||||||
| chr16:11739796 | A | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
85 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.254+2681T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739796 | |||||||
| chr16:11739864 | T | A | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.254+2613A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11739864 | |||||||
| chr16:11740002 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.254+2475C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740002 | |||||||
| chr16:11740030 | G | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
205 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.254+2447C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740030 | |||||||
| chr16:11740146 | TA | T | 53 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
60 | HG00408.hp1 HG00544.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.254+2330delT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740146 | |||||||
| chr16:11740147 | A | T | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+2330T>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740147 | |||||||
| chr16:11740228 | C | CG | 9 | a0001c0001t0001g0077 a0001c0001t0001g0203 a0001c0001t0001g0204 others(6): Show |
9 | HG00423.hp1 HG02027.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+2248dupC | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740228 | |||||||
| chr16:11740228 | C | G | 1 | a0016c0016t0001g0027 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.254+2249G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740228 | |||||||
| chr16:11740350 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.254+2127G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740350 | |||||||
| chr16:11740552 | T | TA | 3 | a0001c0001t0001g0265 a0007c0013t0001g0115 a0007c0013t0001g0116 |
3 | HG02145.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.254+1924dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740552 | |||||||
| chr16:11740600 | A | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
9 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+1877T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740600 | |||||||
| chr16:11740625 | T | G | 2 | a0001c0004t0001g0031 a0001c0004t0001g0032 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.254+1852A>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740625 | |||||||
| chr16:11740816 | T | A | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+1661A>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740816 | |||||||
| chr16:11740931 | G | A | 14 | a0002c0005t0001g0009 a0002c0005t0001g0033 a0002c0005t0001g0034 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+1546C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740931 | |||||||
| chr16:11740965 | T | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.254+1512A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740965 | |||||||
| chr16:11740982 | T | C | 1 | a0002c0003t0001g0200 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.254+1495A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11740982 | |||||||
| chr16:11741011 | T | TA | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.254+1465dupT | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741011 | |||||||
| chr16:11741042 | A | G | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.254+1435T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741042 | |||||||
| chr16:11741075 | T | C | 23 | a0001c0004t0001g0002 a0001c0004t0001g0010 a0001c0004t0001g0046 others(20): Show |
27 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.254+1402A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741075 | |||||||
| chr16:11741144 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0024t0001g0076 |
3 | NA18988.hp1 NA19075.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.254+1333G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741144 | |||||||
| chr16:11741291 | T | C | 1 | a0003c0002t0001g0338 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.254+1186A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741291 | |||||||
| chr16:11741353 | C | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
157 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.254+1124G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741353 | |||||||
| chr16:11741364 | G | T | 2 | a0001c0001t0001g0118 a0002c0003t0001g0117 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.254+1113C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741364 | |||||||
| chr16:11741387 | G | C | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+1090C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741387 | |||||||
| chr16:11741403 | C | G | 51 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(48): Show |
55 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.254+1074G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741403 | |||||||
| chr16:11741469 | G | C | 3 | a0006c0010t0001g0266 a0006c0010t0001g0267 a0006c0010t0001g0268 |
3 | HG02615.hp2 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.254+1008C>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741469 | |||||||
| chr16:11741544 | C | A | 4 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | NA18612.hp2 NA18994.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+933G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741544 | |||||||
| chr16:11741659 | C | G | 1 | a0010c0028t0001g0269 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.254+818G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741659 | |||||||
| chr16:11741823 | A | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
159 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.254+654T>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741823 | |||||||
| chr16:11741867 | T | C | 2 | a0002c0003t0001g0201 a0002c0003t0001g0202 |
2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.254+610A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741867 | |||||||
| chr16:11741888 | C | G | 1 | a0001c0014t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.254+589G>C | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741888 | |||||||
| chr16:11741985 | T | C | 2 | a0002c0011t0001g0067 a0002c0011t0001g0068 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254+492A>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11741985 | |||||||
| chr16:11742000 | C | A | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+477G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742000 | |||||||
| chr16:11742007 | G | T | 4 | a0001c0007t0001g0008 a0001c0007t0001g0028 a0001c0007t0001g0029 others(1): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+470C>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742007 | |||||||
| chr16:11742090 | C | A | 69 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(66): Show |
77 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.254+387G>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742090 | |||||||
| chr16:11742194 | A | C | 4 | a0002c0003t0002g0069 a0002c0003t0002g0070 a0002c0003t0002g0071 others(1): Show |
4 | NA19058.hp1 NA19080.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+283T>G | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742194 | |||||||
| chr16:11742232 | C | T | 6 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0007t0001g0008 others(3): Show |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.254+245G>A | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742232 | |||||||
| chr16:11742324 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.254+153C>T | TXNDC11 | ENSG00000153066.13 | transcript | ENST00000283033.10 | protein_coding | 1/11 | chr16 | 11742324 |