Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25828 |
| ensemblid | ENSG00000100348.10 |
| hgncid | 17772 |
| symbol | TXN2 |
| name | thioredoxin 2 |
| refseq_nuc | NM_012473.4 |
| refseq_prot | NP_036605.2 |
| ensembl_nuc | ENST00000216185.7 |
| ensembl_prot | ENSP00000216185.2 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 36467046 |
| end | 36481640 |
| strand | - |
| ver | v1.2 |
| region | chr22:36467046-36481640 |
| region5000 | chr22:36462046-36486640 |
| regionname0 | TXN2_chr22_36467046_36481640 |
| regionname5000 | TXN2_chr22_36462046_36486640 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 166 | 338 | 93 | 62 | 137 | 10 | 34 | 115 | TXN2_chr22_36462046_36486640 | TXN2 | MAQRL others(161): Show |
chr22 | 36462046 | 36486640 |
| a0002 | 0/0 | 166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | MAQRL others(161): Show |
chr22 | 36462046 | 36486640 |
| a0003 | 0/0 | 166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | MAQRL others(161): Show |
chr22 | 36462046 | 36486640 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 498 | 334 | 91 | 60 | 137 | 10 | 34 | TXN2_chr22_36462046_36486640 | TXN2 | ATGGC others(493): Show |
chr22 | 36462046 | 36486640 | ||
| a0001c0002 | 0/0 | 498 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | ATGGC others(493): Show |
chr22 | 36462046 | 36486640 | ||
| a0001c0003 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | ATGGC others(493): Show |
chr22 | 36462046 | 36486640 | ||
| a0001c0005 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | ATGGC others(493): Show |
chr22 | 36462046 | 36486640 | ||
| a0002c0004 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | ATGGC others(493): Show |
chr22 | 36462046 | 36486640 | ||
| a0003c0006 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | ATGGC others(493): Show |
chr22 | 36462046 | 36486640 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1336 | 260 | 71 | 50 | 98 | 9 | 30 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0002 | 0/0 | 1336 | 31 | 0 | 6 | 25 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0003 | 0/0 | 1336 | 17 | 14 | 2 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0004 | 0/0 | 1336 | 13 | 2 | 0 | 10 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0005 | 0/0 | 1336 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0006 | 0/0 | 1336 | 2 | 0 | 1 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0007 | 0/0 | 1336 | 2 | 0 | 0 | 0 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0008 | 0/0 | 1336 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0009 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0010 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0011 | 0/0 | 1336 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0012 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0001t0013 | 0/0 | 1336 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0002t0001 | 0/0 | 1336 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0003t0001 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0001c0005t0001 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0002c0004t0001 | 0/0 | 1336 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| a0003c0006t0001 | 0/0 | 1336 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | GAGGA others(1331): Show |
chr22 | 36462046 | 36486640 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 67 | 2 | 8 | 46 | 0 | 10 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0002 | 0/0 | 37 | 1 | 18 | 9 | 4 | 5 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0003 | 0/0 | 16 | 16 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0005 | 0/0 | 13 | 5 | 4 | 0 | 2 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0006 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0013 | 0/0 | 5 | 1 | 1 | 0 | 0 | 3 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0004 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0004g0007 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0006g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0001c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0002c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| a0003c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0073 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03491 | hp2 | a0001 | c0001 | t0013 | g0124 | SAS | PJL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0061 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0057 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18522 | hp1 | a0002 | c0004 | t0001 | g0052 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18962 | hp1 | a0001 | c0001 | t0012 | g0093 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18998 | hp2 | a0003 | c0006 | t0001 | g0123 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0086 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0027 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0122 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | USA | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0099 | REF | REF | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | TXN2_chr22_36462046_36486640 | TXN2 | chr22 | 36462046 | 36486640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36476771 | C | T | 1 | a0002 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.349G>A | p.Asp117Asn | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/4 | 426/1336 | 349/501 | 117/166 | chr22 | 36476771 | |||
| chr22:36480682 | T | C | 1 | a0003 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.156A>G | p.Ile52Met | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/4 | 233/1336 | 156/501 | 52/166 | chr22 | 36480682 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36476826 | C | T | 1 | a0001c0002 | 2 | HG01256.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.294G>A | p.Pro98Pro | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/4 | 371/1336 | 294/501 | 98/166 | chr22 | 36476826 | |||
| chr22:36480580 | G | A | 1 | a0001c0005 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.258C>T | p.His86His | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/4 | 335/1336 | 258/501 | 86/166 | chr22 | 36480580 | |||
| chr22:36480805 | C | T | 1 | a0001c0003 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.33G>A | p.Leu11Leu | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/4 | 110/1336 | 33/501 | 11/166 | chr22 | 36480805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36467049 | G | A | 1 | a0001c0001t0007 | 2 | HG03688.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*755C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 755 | chr22 | 36467049 | ||||||
| chr22:36467099 | G | T | 1 | a0001c0001t0008 | 2 | HG02818.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*705C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 705 | chr22 | 36467099 | ||||||
| chr22:36467113 | C | T | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(1): Show |
34 | HG01167.hp2 HG01168.hp1 HG01884.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 691 | chr22 | 36467113 | ||||||
| chr22:36467114 | G | A | 1 | a0001c0001t0010 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*690C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 690 | chr22 | 36467114 | ||||||
| chr22:36467267 | A | T | 1 | a0001c0001t0009 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 537 | chr22 | 36467267 | ||||||
| chr22:36467328 | C | A | 1 | a0001c0001t0002 | 31 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*476G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 476 | chr22 | 36467328 | ||||||
| chr22:36467341 | G | C | 1 | a0001c0001t0011 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 463 | chr22 | 36467341 | ||||||
| chr22:36467439 | G | A | 1 | a0001c0001t0012 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 365 | chr22 | 36467439 | ||||||
| chr22:36467444 | G | A | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 |
32 | HG01167.hp2 HG01168.hp1 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*360C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 360 | chr22 | 36467444 | ||||||
| chr22:36467552 | T | C | 1 | a0001c0001t0013 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 252 | chr22 | 36467552 | ||||||
| chr22:36467658 | C | T | 2 | a0001c0001t0004 a0001c0001t0007 |
15 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 146 | chr22 | 36467658 | ||||||
| chr22:36467679 | C | G | 1 | a0001c0001t0006 | 2 | HG01167.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 4/4 | 125 | chr22 | 36467679 | ||||||
| chr22:36481597 | T | C | 1 | a0001c0001t0013 | 1 | HG03491.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/4 | chr22 | 36481597 | |||||||
| chr22:36481632 | C | G | 1 | a0001c0001t0005 | 2 | HG02559.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-69G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/4 | 795 | chr22 | 36481632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:36468218 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0074 |
6 | HG00642.hp2 HG00741.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-301G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468218 | |||||||
| chr22:36468320 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.388-403G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468320 | |||||||
| chr22:36468324 | C | G | 1 | a0001c0001t0003g0103 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.388-407G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468324 | |||||||
| chr22:36468343 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.388-426G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468343 | |||||||
| chr22:36468369 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.388-452T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468369 | |||||||
| chr22:36468433 | T | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(8): Show |
30 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.388-516A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468433 | |||||||
| chr22:36468564 | A | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0044 others(8): Show |
27 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.388-647T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468564 | |||||||
| chr22:36468570 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.388-653G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468570 | |||||||
| chr22:36468640 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-723C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468640 | |||||||
| chr22:36468644 | G | C | 5 | a0001c0001t0003g0009 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-727C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468644 | |||||||
| chr22:36468720 | CA | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-804delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468720 | |||||||
| chr22:36468851 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.388-934C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468851 | |||||||
| chr22:36468910 | C | T | 1 | a0001c0001t0004g0056 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.388-993G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36468910 | |||||||
| chr22:36469039 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.388-1122G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469039 | |||||||
| chr22:36469041 | C | CATAA | 10 | a0001c0001t0001g0087 a0001c0001t0001g0119 a0001c0001t0002g0004 others(7): Show |
27 | HG00738.hp2 HG01069.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.388-1128_388-1125d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469041 | |||||||
| chr22:36469041 | C | CATAAATA others(1): Show |
3 | a0001c0001t0002g0011 a0001c0001t0002g0036 a0001c0001t0002g0097 |
7 | HG01069.hp2 HG01071.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-1132_388-1125d others(10): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469041 | |||||||
| chr22:36469041 | C | CATAAATA others(5): Show |
2 | a0001c0001t0001g0029 a0002c0004t0001g0052 |
3 | NA18522.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.388-1136_388-1125d others(14): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469041 | |||||||
| chr22:36469061 | AATAAATA others(5): Show |
A | 16 | a0001c0001t0003g0009 a0001c0001t0003g0024 a0001c0001t0003g0058 others(13): Show |
31 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.388-1156_388-1145d others(14): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469061 | |||||||
| chr22:36469069 | A | AATAC | 15 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0030 others(12): Show |
30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.388-1156_388-1153d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469069 | |||||||
| chr22:36469069 | AATAC | A | 2 | a0001c0001t0001g0010 a0001c0001t0005g0021 |
8 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-1156_388-1153d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469069 | |||||||
| chr22:36469073 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0043 others(5): Show |
21 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.388-1156G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469073 | |||||||
| chr22:36469102 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0041 others(11): Show |
30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.388-1185C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469102 | |||||||
| chr22:36469105 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1188G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469105 | |||||||
| chr22:36469112 | C | T | 10 | a0001c0001t0003g0024 a0001c0001t0003g0058 a0001c0001t0004g0007 others(7): Show |
18 | HG02572.hp2 HG02717.hp1 HG03209.hp2 others(15): Show |
intron_variant | MODIFIER | c.388-1195G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469112 | |||||||
| chr22:36469133 | G | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(13): Show |
33 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(30): Show |
intron_variant | MODIFIER | c.388-1216C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469133 | |||||||
| chr22:36469140 | C | A | 1 | a0001c0001t0002g0040 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.388-1223G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469140 | |||||||
| chr22:36469151 | G | T | 17 | a0001c0001t0003g0009 a0001c0001t0003g0024 a0001c0001t0003g0058 others(14): Show |
32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-1234C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469151 | |||||||
| chr22:36469172 | C | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-1255G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469172 | |||||||
| chr22:36469261 | C | T | 7 | a0001c0001t0003g0058 a0001c0001t0004g0007 a0001c0001t0004g0060 others(4): Show |
14 | HG03688.hp1 HG03834.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.388-1344G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469261 | |||||||
| chr22:36469338 | A | G | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1421T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469338 | |||||||
| chr22:36469409 | ACT | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(17): Show |
72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.388-1494_388-1493d others(4): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469409 | |||||||
| chr22:36469550 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0068 others(1): Show |
9 | HG00558.hp1 NA18944.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.388-1633A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469550 | |||||||
| chr22:36469557 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1640A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469557 | |||||||
| chr22:36469566 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1649A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469566 | |||||||
| chr22:36469575 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1658G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469575 | |||||||
| chr22:36469597 | T | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-1680A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469597 | |||||||
| chr22:36469737 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.388-1820G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469737 | |||||||
| chr22:36469749 | A | T | 17 | a0001c0001t0003g0009 a0001c0001t0003g0024 a0001c0001t0003g0058 others(14): Show |
32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-1832T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469749 | |||||||
| chr22:36469753 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.388-1836G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469753 | |||||||
| chr22:36469785 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.388-1868C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469785 | |||||||
| chr22:36469815 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.388-1898C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469815 | |||||||
| chr22:36469881 | G | A | 5 | a0001c0001t0003g0009 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-1964C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36469881 | |||||||
| chr22:36470054 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388-2137T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470054 | |||||||
| chr22:36470095 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-2178G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470095 | |||||||
| chr22:36470181 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.388-2264G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470181 | |||||||
| chr22:36470230 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(42): Show |
97 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.388-2313G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470230 | |||||||
| chr22:36470273 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-2356G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470273 | |||||||
| chr22:36470362 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(15): Show |
47 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.388-2445C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470362 | |||||||
| chr22:36470451 | A | G | 1 | a0001c0001t0003g0024 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.388-2534T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470451 | |||||||
| chr22:36470560 | TAAG | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-2646_388-2644d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470560 | |||||||
| chr22:36470567 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.388-2650A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470567 | |||||||
| chr22:36470643 | C | A | 1 | a0001c0001t0003g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.388-2726G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470643 | |||||||
| chr22:36470660 | C | G | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-2743G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470660 | |||||||
| chr22:36470684 | C | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-2767G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470684 | |||||||
| chr22:36470761 | C | T | 13 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0003g0024 others(10): Show |
21 | HG02572.hp1 HG02572.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.388-2844G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470761 | |||||||
| chr22:36470781 | T | TAAA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-2867_388-2865d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470781 | |||||||
| chr22:36470781 | TA | T | 7 | a0001c0001t0001g0055 a0001c0001t0001g0075 a0001c0001t0001g0082 others(4): Show |
7 | HG02109.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-2865delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470781 | |||||||
| chr22:36470885 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.388-2968G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470885 | |||||||
| chr22:36470903 | T | C | 1 | a0001c0003t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-2986A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470903 | |||||||
| chr22:36470932 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.388-3015T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470932 | |||||||
| chr22:36470963 | GCATACAC others(19): Show |
G | 2 | a0001c0001t0002g0097 a0001c0001t0008g0028 |
3 | HG02135.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.388-3072_388-3047d others(28): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36470963 | |||||||
| chr22:36471049 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0045 others(3): Show |
18 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.388-3132G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471049 | |||||||
| chr22:36471063 | C | T | 1 | a0001c0003t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-3146G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471063 | |||||||
| chr22:36471086 | T | C | 17 | a0001c0001t0003g0009 a0001c0001t0003g0024 a0001c0001t0003g0058 others(14): Show |
32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-3169A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471086 | |||||||
| chr22:36471182 | TG | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0119 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-3266delC | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471182 | |||||||
| chr22:36471317 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.388-3400C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471317 | |||||||
| chr22:36471320 | G | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0119 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-3403C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471320 | |||||||
| chr22:36471399 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.388-3482A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471399 | |||||||
| chr22:36471400 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.388-3483G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471400 | |||||||
| chr22:36471417 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-3500G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471417 | |||||||
| chr22:36471549 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.388-3632C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471549 | |||||||
| chr22:36471623 | C | G | 1 | a0001c0001t0002g0037 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.388-3706G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471623 | |||||||
| chr22:36471689 | A | C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(24): Show |
61 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-3772T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471689 | |||||||
| chr22:36471705 | CTGCCTGT others(1331): Show |
C | 1 | a0001c0001t0002g0033 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.387+3690_388-3789d others(2): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471705 | |||||||
| chr22:36471708 | C | A | 1 | a0001c0001t0001g0029 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.388-3791G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471708 | |||||||
| chr22:36471748 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0075 |
2 | NA18986.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.388-3831G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471748 | |||||||
| chr22:36471771 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.388-3854G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471771 | |||||||
| chr22:36471784 | T | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(45): Show |
100 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.388-3867A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471784 | |||||||
| chr22:36471812 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.388-3895A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471812 | |||||||
| chr22:36471826 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0101 |
3 | HG02135.hp1 NA18980.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.388-3909G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471826 | |||||||
| chr22:36471827 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.388-3910C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471827 | |||||||
| chr22:36471842 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
6 | HG00741.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-3925G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471842 | |||||||
| chr22:36471843 | G | A | 17 | a0001c0001t0003g0009 a0001c0001t0003g0024 a0001c0001t0003g0058 others(14): Show |
32 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.388-3926C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471843 | |||||||
| chr22:36471892 | T | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(26): Show |
64 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.388-3975A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471892 | |||||||
| chr22:36471895 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.388-3978C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471895 | |||||||
| chr22:36471956 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(43): Show |
98 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.388-4039A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471956 | |||||||
| chr22:36471968 | T | TA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(19): Show |
46 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.388-4052dupT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | |||||||
| chr22:36471968 | T | TAA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(8): Show |
19 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.388-4053_388-4052d others(4): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | |||||||
| chr22:36471968 | T | TAAA | 8 | a0001c0001t0003g0058 a0001c0001t0004g0007 a0001c0001t0004g0059 others(5): Show |
15 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.388-4054_388-4052d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | |||||||
| chr22:36471968 | TA | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(2): Show |
6 | HG02683.hp2 HG02895.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-4052delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471968 | |||||||
| chr22:36471976 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.388-4059T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471976 | |||||||
| chr22:36471982 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.388-4065T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36471982 | |||||||
| chr22:36472057 | CA | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0050 others(5): Show |
23 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-4141delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472057 | |||||||
| chr22:36472123 | G | A | 1 | a0001c0003t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-4206C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472123 | |||||||
| chr22:36472145 | A | G | 5 | a0001c0001t0003g0009 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-4228T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472145 | |||||||
| chr22:36472213 | G | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(26): Show |
66 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.388-4296C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472213 | |||||||
| chr22:36472272 | C | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 |
4 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-4355G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472272 | |||||||
| chr22:36472519 | C | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0029 others(16): Show |
37 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.387+4214G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472519 | |||||||
| chr22:36472588 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
29 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.387+4145G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472588 | |||||||
| chr22:36472819 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.387+3914C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472819 | |||||||
| chr22:36472822 | C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+3911G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472822 | |||||||
| chr22:36472841 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 |
4 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+3892A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472841 | |||||||
| chr22:36472857 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
28 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.387+3876G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472857 | |||||||
| chr22:36472874 | GTCCGGGG others(21): Show |
G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(20): Show |
59 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.387+3831_387+3858d others(30): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472874 | |||||||
| chr22:36472966 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(79): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.387+3767G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472966 | |||||||
| chr22:36472992 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(81): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.387+3741A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36472992 | |||||||
| chr22:36473032 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0048 |
2 | HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.387+3701G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473032 | |||||||
| chr22:36473046 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.387+3687G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473046 | |||||||
| chr22:36473077 | TGGGCGAA others(129): Show |
T | 1 | a0001c0001t0001g0116 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.387+3520_387+3655d others(2): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473077 | |||||||
| chr22:36473190 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0003g0024 |
3 | HG02572.hp2 HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.387+3543G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473190 | |||||||
| chr22:36473200 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.387+3533A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473200 | |||||||
| chr22:36473304 | G | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+3429C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473304 | |||||||
| chr22:36473350 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.387+3383C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473350 | |||||||
| chr22:36473365 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0050 others(4): Show |
23 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.387+3368G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473365 | |||||||
| chr22:36473422 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.387+3311C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473422 | |||||||
| chr22:36473444 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0050 others(3): Show |
21 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.387+3289T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473444 | |||||||
| chr22:36473591 | G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+3142C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473591 | |||||||
| chr22:36473646 | G | A | 1 | a0002c0004t0001g0052 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387+3087C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473646 | |||||||
| chr22:36473668 | A | G | 1 | a0001c0001t0003g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.387+3065T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473668 | |||||||
| chr22:36473843 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.387+2890G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473843 | |||||||
| chr22:36473848 | G | A | 7 | a0001c0001t0003g0058 a0001c0001t0004g0007 a0001c0001t0004g0056 others(4): Show |
14 | HG03209.hp2 HG03834.hp1 NA18940.hp1 others(11): Show |
intron_variant | MODIFIER | c.387+2885C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473848 | |||||||
| chr22:36473880 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(6): Show |
27 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.387+2853C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473880 | |||||||
| chr22:36473890 | A | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2843T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36473890 | |||||||
| chr22:36474051 | C | T | 1 | a0001c0003t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.387+2682G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474051 | |||||||
| chr22:36474283 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(90): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.387+2450A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474283 | |||||||
| chr22:36474420 | T | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2313A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474420 | |||||||
| chr22:36474424 | T | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.387+2309A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474424 | |||||||
| chr22:36474457 | T | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2276A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474457 | |||||||
| chr22:36474498 | T | G | 8 | a0001c0001t0003g0058 a0001c0001t0004g0007 a0001c0001t0004g0059 others(5): Show |
15 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.387+2235A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474498 | |||||||
| chr22:36474535 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(6): Show |
27 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.387+2198G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474535 | |||||||
| chr22:36474572 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2161G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474572 | |||||||
| chr22:36474585 | A | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+2148T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474585 | |||||||
| chr22:36474740 | C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+1993G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474740 | |||||||
| chr22:36474749 | C | T | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0003g0009 others(4): Show |
14 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.387+1984G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474749 | |||||||
| chr22:36474750 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.387+1983C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474750 | |||||||
| chr22:36474774 | A | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+1959T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474774 | |||||||
| chr22:36474796 | T | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0029 others(40): Show |
90 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+1937A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474796 | |||||||
| chr22:36474798 | A | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0029 others(40): Show |
90 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+1935T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474798 | |||||||
| chr22:36474835 | G | T | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387+1898C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474835 | |||||||
| chr22:36474906 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.387+1827G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474906 | |||||||
| chr22:36474991 | T | G | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+1742A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36474991 | |||||||
| chr22:36475011 | T | C | 1 | a0001c0001t0001g0029 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.387+1722A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475011 | |||||||
| chr22:36475097 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.387+1636C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475097 | |||||||
| chr22:36475115 | C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+1618G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475115 | |||||||
| chr22:36475222 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1511T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475222 | |||||||
| chr22:36475224 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1509T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475224 | |||||||
| chr22:36475226 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1507T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475226 | |||||||
| chr22:36475227 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1506T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475227 | |||||||
| chr22:36475235 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1498G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475235 | |||||||
| chr22:36475235 | C | CG | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.387+1497dupC | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475235 | |||||||
| chr22:36475236 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1497C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475236 | |||||||
| chr22:36475237 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1496C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475237 | |||||||
| chr22:36475238 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1495G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475238 | |||||||
| chr22:36475239 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1494C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475239 | |||||||
| chr22:36475241 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.387+1492C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475241 | |||||||
| chr22:36475242 | GTGGCGCG others(5): Show |
G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1479_387+1490d others(14): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475242 | |||||||
| chr22:36475261 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1472A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475261 | |||||||
| chr22:36475262 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1471G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475262 | |||||||
| chr22:36475265 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1468G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475265 | |||||||
| chr22:36475267 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1466T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475267 | |||||||
| chr22:36475269 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1464A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475269 | |||||||
| chr22:36475270 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1463G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475270 | |||||||
| chr22:36475271 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1462G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475271 | |||||||
| chr22:36475273 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1460C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475273 | |||||||
| chr22:36475274 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1459T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475274 | |||||||
| chr22:36475275 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1458C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475275 | |||||||
| chr22:36475276 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1457C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475276 | |||||||
| chr22:36475277 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1456G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475277 | |||||||
| chr22:36475277 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG03130.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.387+1456G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475277 | |||||||
| chr22:36475278 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1455A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475278 | |||||||
| chr22:36475279 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1454C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475279 | |||||||
| chr22:36475286 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1447C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475286 | |||||||
| chr22:36475291 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1442G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475291 | |||||||
| chr22:36475293 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1440C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475293 | |||||||
| chr22:36475294 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1439G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475294 | |||||||
| chr22:36475304 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1429C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475304 | |||||||
| chr22:36475308 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1425C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475308 | |||||||
| chr22:36475309 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1424G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475309 | |||||||
| chr22:36475314 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1419C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475314 | |||||||
| chr22:36475320 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1413C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475320 | |||||||
| chr22:36475323 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1410T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475323 | |||||||
| chr22:36475324 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1409C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475324 | |||||||
| chr22:36475325 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1408G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475325 | |||||||
| chr22:36475327 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1406C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475327 | |||||||
| chr22:36475333 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1400C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475333 | |||||||
| chr22:36475336 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1397G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475336 | |||||||
| chr22:36475337 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1396G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475337 | |||||||
| chr22:36475339 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1394G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475339 | |||||||
| chr22:36475341 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1392C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475341 | |||||||
| chr22:36475342 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1391G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475342 | |||||||
| chr22:36475344 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1389G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475344 | |||||||
| chr22:36475346 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1387G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475346 | |||||||
| chr22:36475347 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1386G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475347 | |||||||
| chr22:36475349 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1384C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475349 | |||||||
| chr22:36475353 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1380C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475353 | |||||||
| chr22:36475355 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1378C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475355 | |||||||
| chr22:36475359 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1374G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475359 | |||||||
| chr22:36475362 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1371C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475362 | |||||||
| chr22:36475363 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1370T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475363 | |||||||
| chr22:36475366 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1367T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475366 | |||||||
| chr22:36475370 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1363G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475370 | |||||||
| chr22:36475378 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1355G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475378 | |||||||
| chr22:36475380 | A | ATCTAAAT others(3): Show |
1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1352_387+1353i others(12): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475380 | |||||||
| chr22:36475386 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1347G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475386 | |||||||
| chr22:36475389 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1344T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475389 | |||||||
| chr22:36475392 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1341G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475392 | |||||||
| chr22:36475393 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1340G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475393 | |||||||
| chr22:36475394 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1339G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475394 | |||||||
| chr22:36475395 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1338A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475395 | |||||||
| chr22:36475396 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1337C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475396 | |||||||
| chr22:36475398 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1335G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475398 | |||||||
| chr22:36475399 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1334A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475399 | |||||||
| chr22:36475405 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1328C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475405 | |||||||
| chr22:36475409 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1324A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475409 | |||||||
| chr22:36475412 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1321A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475412 | |||||||
| chr22:36475417 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1316A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475417 | |||||||
| chr22:36475418 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1315G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475418 | |||||||
| chr22:36475419 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1314G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475419 | |||||||
| chr22:36475420 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1313A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475420 | |||||||
| chr22:36475422 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1311A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475422 | |||||||
| chr22:36475433 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+1300A>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475433 | |||||||
| chr22:36475524 | A | C | 5 | a0001c0001t0003g0009 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.387+1209T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475524 | |||||||
| chr22:36475667 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0075 a0001c0001t0012g0093 |
5 | NA18947.hp2 NA18962.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+1066A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475667 | |||||||
| chr22:36475832 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.387+901G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475832 | |||||||
| chr22:36475910 | TTCTC | T | 1 | a0001c0001t0001g0010 | 6 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+819_387+822del others(4): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475910 | |||||||
| chr22:36475920 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG03130.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.387+813G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36475920 | |||||||
| chr22:36476067 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.387+666T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476067 | |||||||
| chr22:36476211 | C | T | 1 | a0001c0001t0001g0026 | 2 | NA18943.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.387+522G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476211 | |||||||
| chr22:36476474 | C | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+259G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476474 | |||||||
| chr22:36476517 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.387+216C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476517 | |||||||
| chr22:36476540 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.387+193G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476540 | |||||||
| chr22:36476583 | T | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+150A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476583 | |||||||
| chr22:36476587 | G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.387+146C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476587 | |||||||
| chr22:36476703 | T | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(81): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.387+30A>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 3/3 | chr22 | 36476703 | |||||||
| chr22:36476955 | CTTA | C | 9 | a0001c0001t0003g0058 a0001c0001t0004g0007 a0001c0001t0004g0056 others(6): Show |
16 | HG03209.hp2 HG03688.hp1 HG03834.hp1 others(13): Show |
intron_variant | MODIFIER | c.264-102_264-100del others(3): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36476955 | |||||||
| chr22:36477075 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.264-219G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477075 | |||||||
| chr22:36477210 | C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264-354G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477210 | |||||||
| chr22:36477238 | C | G | 28 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0054 others(25): Show |
57 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.264-382G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477238 | |||||||
| chr22:36477450 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
28 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.264-594G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477450 | |||||||
| chr22:36477460 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.264-604C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477460 | |||||||
| chr22:36477572 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.264-716T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477572 | |||||||
| chr22:36477676 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.264-820G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477676 | |||||||
| chr22:36477775 | A | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264-919T>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477775 | |||||||
| chr22:36477864 | C | T | 28 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0054 others(25): Show |
57 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.264-1008G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477864 | |||||||
| chr22:36477920 | T | C | 1 | a0001c0001t0004g0060 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.264-1064A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477920 | |||||||
| chr22:36477966 | G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264-1110C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477966 | |||||||
| chr22:36477968 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.264-1112G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477968 | |||||||
| chr22:36477976 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.264-1120T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477976 | |||||||
| chr22:36477999 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.264-1143A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36477999 | |||||||
| chr22:36478132 | C | CA | 29 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(26): Show |
66 | HG00558.hp1 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.264-1277dupT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478132 | |||||||
| chr22:36478132 | C | CAAA | 5 | a0001c0001t0003g0009 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
12 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.264-1279_264-1277d others(5): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478132 | |||||||
| chr22:36478132 | CA | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0067 others(5): Show |
24 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.264-1277delT | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478132 | |||||||
| chr22:36478176 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG00741.hp2 HG02109.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-1320G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478176 | |||||||
| chr22:36478463 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0003g0024 |
3 | HG02572.hp2 HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.264-1607C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478463 | |||||||
| chr22:36478495 | CTTAT | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0117 a0001c0005t0001g0122 |
4 | HG02486.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-1643_264-1640d others(6): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478495 | |||||||
| chr22:36478552 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(29): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.264-1696G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478552 | |||||||
| chr22:36478553 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0003g0009 a0001c0001t0003g0103 others(3): Show |
13 | HG01168.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-1697C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478553 | |||||||
| chr22:36478630 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.264-1774A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478630 | |||||||
| chr22:36478685 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG03130.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.264-1829C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478685 | |||||||
| chr22:36478733 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.263+1842G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478733 | |||||||
| chr22:36478792 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.263+1783G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478792 | |||||||
| chr22:36478803 | C | G | 1 | a0001c0001t0003g0042 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.263+1772G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478803 | |||||||
| chr22:36478853 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.263+1722G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478853 | |||||||
| chr22:36478880 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.263+1695C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478880 | |||||||
| chr22:36478905 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0029 others(39): Show |
89 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.263+1670G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478905 | |||||||
| chr22:36478909 | A | G | 29 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0054 others(26): Show |
59 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.263+1666T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478909 | |||||||
| chr22:36478974 | C | A | 1 | a0001c0001t0004g0112 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.263+1601G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36478974 | |||||||
| chr22:36479081 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.263+1494G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479081 | |||||||
| chr22:36479334 | CT | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0003g0058 others(9): Show |
19 | HG01256.hp1 HG03209.hp2 HG03491.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+1240delA | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479334 | |||||||
| chr22:36479335 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.263+1240A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479335 | |||||||
| chr22:36479392 | C | T | 1 | a0002c0004t0001g0052 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.263+1183G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479392 | |||||||
| chr22:36479395 | G | A | 1 | a0001c0001t0002g0014 | 4 | NA18747.hp2 NA18950.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.263+1180C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479395 | |||||||
| chr22:36479419 | C | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+1156G>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479419 | |||||||
| chr22:36479449 | A | T | 1 | a0001c0001t0003g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.263+1126T>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479449 | |||||||
| chr22:36479583 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.263+992G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479583 | |||||||
| chr22:36479622 | G | C | 1 | a0001c0003t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.263+953C>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479622 | |||||||
| chr22:36479624 | G | A | 1 | a0001c0001t0003g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.263+951C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479624 | |||||||
| chr22:36479864 | C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+711G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479864 | |||||||
| chr22:36479865 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.263+710C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479865 | |||||||
| chr22:36479882 | CT | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0001t0001g0113 others(2): Show |
7 | NA18948.hp2 NA18969.hp2 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.263+692delA | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479882 | |||||||
| chr22:36479882 | CTT | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0041 others(10): Show |
30 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.263+691_263+692del others(2): Show |
TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36479882 | |||||||
| chr22:36480009 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.263+566C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480009 | |||||||
| chr22:36480041 | G | A | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+534C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480041 | |||||||
| chr22:36480044 | T | C | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+531A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480044 | |||||||
| chr22:36480071 | C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.263+504G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480071 | |||||||
| chr22:36480118 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.263+457C>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480118 | |||||||
| chr22:36480315 | T | C | 1 | a0001c0003t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.263+260A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 2/3 | chr22 | 36480315 | |||||||
| chr22:36481011 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(7): Show |
28 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1-174T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481011 | |||||||
| chr22:36481058 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1-221G>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481058 | |||||||
| chr22:36481123 | T | C | 1 | a0001c0001t0001g0031 | 2 | NA18951.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1-286A>G | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481123 | |||||||
| chr22:36481288 | C | T | 1 | a0001c0001t0005g0021 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-1+276G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481288 | |||||||
| chr22:36481412 | A | G | 11 | a0001c0001t0001g0039 a0001c0001t0002g0004 a0001c0001t0002g0011 others(8): Show |
31 | HG00738.hp2 HG01069.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-1+152T>C | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481412 | |||||||
| chr22:36481514 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG01070.hp1 HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-1+50C>T | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481514 | |||||||
| chr22:36481550 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-1+14G>A | TXN2 | ENSG00000100348.10 | transcript | ENST00000216185.7 | protein_coding | 1/3 | chr22 | 36481550 |