Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51075 |
| ensemblid | ENSG00000213593.10 |
| hgncid | 30739 |
| symbol | TMX2 |
| name | thioredoxin related transmembrane protein 2 |
| refseq_nuc | NM_015959.4 |
| refseq_prot | NP_057043.1 |
| ensembl_nuc | ENST00000278422.9 |
| ensembl_prot | ENSP00000278422.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 57712593 |
| end | 57740973 |
| strand | + |
| ver | v1.2 |
| region | chr11:57712593-57740973 |
| region5000 | chr11:57707593-57745973 |
| regionname0 | TMX2_chr11_57712593_57740973 |
| regionname5000 | TMX2_chr11_57707593_57745973 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 296 | 343 | 86 | 66 | 137 | 14 | 40 | 98 | TMX2_chr11_57707593_57745973 | TMX2 | MAVLA others(291): Show |
chr11 | 57707593 | 57745973 |
| a0002 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | MAVLA others(291): Show |
chr11 | 57707593 | 57745973 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 888 | 342 | 85 | 66 | 137 | 14 | 40 | TMX2_chr11_57707593_57745973 | TMX2 | ATGGC others(883): Show |
chr11 | 57707593 | 57745973 | ||
| a0001c0003 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | ATGGC others(883): Show |
chr11 | 57707593 | 57745973 | ||
| a0002c0002 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | ATGGC others(883): Show |
chr11 | 57707593 | 57745973 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1645 | 270 | 74 | 48 | 111 | 8 | 29 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0002 | 0/0 | 1645 | 56 | 7 | 14 | 19 | 6 | 10 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0003 | 0/0 | 1645 | 4 | 4 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0004 | 0/0 | 1647 | 3 | 0 | 0 | 3 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1642): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0005 | 0/0 | 1645 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0006 | 0/0 | 1645 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0007 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0008 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0009 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0011 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0012 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0001t0013 | 0/0 | 1645 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0001c0003t0010 | 0/0 | 1645 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| a0002c0002t0001 | 0/0 | 1645 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | GAGCA others(1640): Show |
chr11 | 57707593 | 57745973 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0008g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0009g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0001t0013g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0001c0003t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0065 | EUR | GBR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | FIN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0137 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0312 | AMR | PUR | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0213 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0076 | EUR | IBS | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0318 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0253 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0335 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CDX | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03516 | hp1 | a0001 | c0003 | t0010 | g0193 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0088 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | STU | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18948 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19076 | hp2 | a0001 | c0001 | t0012 | g0216 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | GIH | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | USA | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | LWK | TMX2_chr11_57707593_57745973 | TMX2 | chr11 | 57707593 | 57745973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57738023 | A | G | 1 | a0002 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.361A>G | p.Ile121Val | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/8 | 387/1645 | 361/891 | 121/296 | chr11 | 57738023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57737983 | C | T | 1 | a0001c0003 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.321C>T | p.Arg107Arg | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/8 | 347/1645 | 321/891 | 107/296 | chr11 | 57737983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57740254 | C | CTT | 1 | a0001c0001t0004 | 3 | NA18945.hp1 NA18959.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11_*12dupTT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 13 | INFO_REALIGN_3_PRIME | chr11 | 57740254 | |||||
| chr11:57740260 | C | T | 1 | a0001c0001t0013 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 15 | chr11 | 57740260 | ||||||
| chr11:57740264 | G | A | 1 | a0001c0001t0006 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 19 | chr11 | 57740264 | ||||||
| chr11:57740436 | G | T | 1 | a0001c0001t0012 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 191 | chr11 | 57740436 | ||||||
| chr11:57740511 | C | T | 2 | a0001c0001t0002 a0001c0001t0006 |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 266 | chr11 | 57740511 | ||||||
| chr11:57740567 | T | A | 1 | a0001c0001t0007 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*322T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 322 | chr11 | 57740567 | ||||||
| chr11:57740603 | C | T | 1 | a0001c0001t0005 | 2 | HG02129.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*358C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 358 | chr11 | 57740603 | ||||||
| chr11:57740645 | G | C | 1 | a0001c0001t0003 | 4 | HG02451.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*400G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 400 | chr11 | 57740645 | ||||||
| chr11:57740798 | T | G | 1 | a0001c0001t0008 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*553T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 553 | chr11 | 57740798 | ||||||
| chr11:57740809 | C | T | 1 | a0001c0001t0011 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 564 | chr11 | 57740809 | ||||||
| chr11:57740813 | T | C | 1 | a0001c0001t0008 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 568 | chr11 | 57740813 | ||||||
| chr11:57740824 | G | A | 1 | a0001c0001t0009 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 579 | chr11 | 57740824 | ||||||
| chr11:57740907 | C | G | 1 | a0001c0003t0010 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*662C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 8/8 | 662 | chr11 | 57740907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:57712814 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | HG00558.hp2 HG02155.hp2 NA19077.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.189+7C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712814 | |||||||
| chr11:57712828 | T | G | 20 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(17): Show |
20 | HG00673.hp1 HG02056.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.189+21T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712828 | |||||||
| chr11:57712829 | A | AC | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | HG02622.hp1 HG03927.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+26dupC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57712829 | ||||||
| chr11:57712859 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+52C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712859 | |||||||
| chr11:57712985 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.189+178A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57712985 | |||||||
| chr11:57713093 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.189+286C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713093 | |||||||
| chr11:57713151 | C | A | 73 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(70): Show |
73 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.189+344C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713151 | |||||||
| chr11:57713151 | C | G | 2 | a0001c0001t0002g0327 a0001c0001t0002g0328 |
2 | HG01358.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.189+344C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713151 | |||||||
| chr11:57713245 | C | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+438C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713245 | |||||||
| chr11:57713406 | G | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
47 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.189+599G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713406 | |||||||
| chr11:57713546 | C | G | 14 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+739C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713546 | |||||||
| chr11:57713555 | T | C | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0108 others(2): Show |
5 | HG02451.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+748T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713555 | |||||||
| chr11:57713562 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189+755T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713562 | |||||||
| chr11:57713623 | C | T | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+816C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713623 | |||||||
| chr11:57713683 | G | A | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+876G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713683 | |||||||
| chr11:57713864 | C | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+1057C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713864 | |||||||
| chr11:57713866 | A | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0108 others(2): Show |
5 | HG02451.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+1059A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713866 | |||||||
| chr11:57713869 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.189+1062G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57713869 | |||||||
| chr11:57714057 | C | T | 6 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0201 others(3): Show |
6 | HG02145.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+1250C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714057 | |||||||
| chr11:57714122 | T | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01496.hp2 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.189+1315T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714122 | |||||||
| chr11:57714310 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.189+1503C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714310 | |||||||
| chr11:57714332 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.189+1525A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714332 | |||||||
| chr11:57714543 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.189+1736C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714543 | |||||||
| chr11:57714763 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.189+1956T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714763 | |||||||
| chr11:57714886 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+2079C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57714886 | |||||||
| chr11:57714894 | T | TA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0118 others(5): Show |
9 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+2093dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57714894 | ||||||
| chr11:57715179 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.189+2372T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715179 | |||||||
| chr11:57715209 | G | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0125 a0001c0001t0001g0126 |
4 | NA18943.hp2 NA18985.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+2402G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715209 | |||||||
| chr11:57715376 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2569G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715376 | |||||||
| chr11:57715378 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2571G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715378 | |||||||
| chr11:57715379 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2572C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715379 | |||||||
| chr11:57715384 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2577A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715384 | |||||||
| chr11:57715394 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2587T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715394 | |||||||
| chr11:57715395 | C | CAATACGA others(3): Show |
1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2588_189+2589i others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715395 | |||||||
| chr11:57715396 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2589T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715396 | |||||||
| chr11:57715422 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2615A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715422 | |||||||
| chr11:57715430 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2623A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715430 | |||||||
| chr11:57715434 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2627T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715434 | |||||||
| chr11:57715438 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2631T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715438 | |||||||
| chr11:57715455 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.189+2648G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715455 | |||||||
| chr11:57715493 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.189+2686A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715493 | |||||||
| chr11:57715567 | A | T | 75 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.189+2760A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715567 | |||||||
| chr11:57715586 | C | CTTTCTTT others(4): Show |
1 | a0001c0001t0001g0332 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.189+2782_189+2783i others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | ||||||
| chr11:57715586 | C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0094 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+2782_189+2789d others(10): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | ||||||
| chr11:57715586 | C | CTTTTTTT others(2): Show |
56 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0118 others(53): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+2781_189+2789d others(11): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | ||||||
| chr11:57715586 | C | CTTTTTTT others(3): Show |
23 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0001c0001t0001g0112 others(20): Show |
23 | HG02074.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.189+2780_189+2789d others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | ||||||
| chr11:57715586 | C | CTTTTTTT others(4): Show |
139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
143 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.189+2789_189+2790i others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | ||||||
| chr11:57715586 | C | CTTTTTTT others(5): Show |
17 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0227 others(14): Show |
17 | HG01346.hp2 HG01978.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+2789_189+2790i others(14): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715586 | ||||||
| chr11:57715593 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.189+2789_189+2790i others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57715593 | ||||||
| chr11:57715789 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.189+2982C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715789 | |||||||
| chr11:57715864 | A | G | 17 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+3057A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715864 | |||||||
| chr11:57715894 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.189+3087T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715894 | |||||||
| chr11:57715934 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.189+3127G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57715934 | |||||||
| chr11:57716111 | C | CG | 4 | a0001c0001t0001g0031 a0001c0001t0001g0237 a0001c0001t0002g0038 others(1): Show |
4 | HG03927.hp2 NA18994.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+3308dupG | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716111 | ||||||
| chr11:57716147 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(20): Show |
24 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.189+3340T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716147 | |||||||
| chr11:57716185 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.189+3378G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716185 | |||||||
| chr11:57716201 | C | T | 155 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(152): Show |
159 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.189+3394C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716201 | |||||||
| chr11:57716250 | C | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0086 |
2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.189+3443C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716250 | |||||||
| chr11:57716254 | C | T | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02572.hp2 HG02717.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+3447C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716254 | |||||||
| chr11:57716264 | A | AC | 23 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(20): Show |
23 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.189+3466dupC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716264 | ||||||
| chr11:57716338 | G | C | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.189+3531G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716338 | |||||||
| chr11:57716353 | A | C | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3546A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716353 | |||||||
| chr11:57716366 | G | A | 4 | a0001c0001t0003g0108 a0001c0001t0003g0109 a0001c0001t0003g0110 others(1): Show |
4 | HG02451.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+3559G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716366 | |||||||
| chr11:57716366 | G | T | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3559G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716366 | |||||||
| chr11:57716386 | C | CT | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3579_189+3580i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716386 | |||||||
| chr11:57716388 | AGGGGCTG others(42): Show |
A | 1 | a0001c0001t0003g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.189+3629_189+3677d others(51): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716388 | ||||||
| chr11:57716394 | T | TCCTCACT others(22): Show |
1 | a0001c0001t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3587_189+3588i others(31): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716394 | |||||||
| chr11:57716395 | G | C | 56 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3588G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716395 | |||||||
| chr11:57716396 | A | C | 56 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3589A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716396 | |||||||
| chr11:57716397 | C | G | 1 | a0001c0001t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3590C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716397 | |||||||
| chr11:57716397 | C | T | 56 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3590C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716397 | |||||||
| chr11:57716398 | C | G | 1 | a0001c0001t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3591C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716398 | |||||||
| chr11:57716399 | C | A | 56 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3592C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716399 | |||||||
| chr11:57716400 | C | CTT | 56 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3593_189+3594i others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716400 | |||||||
| chr11:57716400 | C | G | 1 | a0001c0001t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3593C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716400 | |||||||
| chr11:57716404 | A | AGTAGGGG others(18): Show |
55 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(52): Show |
55 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.189+3597_189+3598i others(27): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716404 | |||||||
| chr11:57716404 | A | AGTAGGGG others(19): Show |
1 | a0001c0001t0002g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189+3597_189+3598i others(28): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716404 | |||||||
| chr11:57716404 | A | C | 1 | a0001c0001t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3597A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716404 | |||||||
| chr11:57716405 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3598C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716405 | |||||||
| chr11:57716407 | T | A | 1 | a0001c0001t0002g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189+3600T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716407 | |||||||
| chr11:57716408 | C | CA | 56 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3601_189+3602i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716408 | |||||||
| chr11:57716435 | C | G | 1 | a0001c0001t0002g0083 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.189+3628C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716435 | |||||||
| chr11:57716435 | C | T | 56 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+3628C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716435 | |||||||
| chr11:57716451 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.189+3644C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716451 | |||||||
| chr11:57716480 | C | T | 17 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+3673C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716480 | |||||||
| chr11:57716481 | G | C | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3674G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716481 | |||||||
| chr11:57716485 | T | A | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3678T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716485 | |||||||
| chr11:57716517 | C | CGGGCAGA others(120): Show |
169 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(166): Show |
173 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.189+3769_189+3770i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | ||||||
| chr11:57716517 | C | CGGGCAGA others(120): Show |
1 | a0001c0001t0001g0198 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189+3769_189+3770i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | ||||||
| chr11:57716517 | C | CGGGCAGA others(121): Show |
4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0225 others(1): Show |
4 | HG03831.hp2 HG03927.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+3769_189+3770i others(130): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | ||||||
| chr11:57716517 | C | CGGGCAGA others(121): Show |
2 | a0001c0001t0001g0199 a0001c0001t0001g0226 |
2 | HG02056.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.189+3761_189+3762i others(130): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | ||||||
| chr11:57716517 | C | CGGGCAGA others(120): Show |
17 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+3754_189+3755i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | ||||||
| chr11:57716517 | C | CGGGCAGA others(119): Show |
1 | a0001c0001t0001g0324 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.189+3733_189+3734i others(128): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716517 | ||||||
| chr11:57716517 | C | T | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+3710C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716517 | |||||||
| chr11:57716527 | C | CGCCCCTC others(120): Show |
1 | a0001c0001t0001g0204 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.189+3769_189+3770i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716527 | ||||||
| chr11:57716528 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.189+3721G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716528 | |||||||
| chr11:57716551 | G | GGCTGGCC others(120): Show |
1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+3754_189+3755i others(129): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716551 | ||||||
| chr11:57716562 | C | CGGGGGGC others(121): Show |
1 | a0001c0001t0001g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.189+3769_189+3770i others(130): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716562 | ||||||
| chr11:57716574 | CCCACCTC others(137): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189+3770_189+3913d others(2): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716574 | ||||||
| chr11:57716581 | C | CCCTCCCG others(71): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0118 |
3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3797_189+3798i others(80): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716581 | ||||||
| chr11:57716591 | C | T | 6 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+3784C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716591 | |||||||
| chr11:57716608 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0118 |
3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3801T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716608 | |||||||
| chr11:57716610 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0139 others(3): Show |
7 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+3803G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716610 | |||||||
| chr11:57716619 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+3812C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716619 | |||||||
| chr11:57716640 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0118 |
3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3833C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716640 | |||||||
| chr11:57716655 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0118 |
3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3848A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716655 | |||||||
| chr11:57716657 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0118 |
3 | HG02451.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+3850C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716657 | |||||||
| chr11:57716658 | G | C | 75 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.189+3851G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716658 | |||||||
| chr11:57716698 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.189+3891A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716698 | |||||||
| chr11:57716723 | C | A | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+3916C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716723 | |||||||
| chr11:57716743 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189+3936T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716743 | |||||||
| chr11:57716752 | A | C | 1 | a0001c0001t0001g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.189+3945A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716752 | |||||||
| chr11:57716779 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.189+3972A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716779 | |||||||
| chr11:57716843 | A | AC | 20 | a0001c0001t0001g0029 a0001c0001t0001g0091 a0001c0001t0001g0092 others(17): Show |
20 | HG01496.hp2 HG01884.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+4044dupC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57716843 | ||||||
| chr11:57716889 | G | T | 17 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG01496.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+4082G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716889 | |||||||
| chr11:57716992 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.189+4185G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57716992 | |||||||
| chr11:57717015 | CTCCCAGA others(109): Show |
C | 6 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+4216_189+4331d others(2): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717015 | ||||||
| chr11:57717032 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.189+4225G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717032 | |||||||
| chr11:57717035 | C | T | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+4228C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717035 | |||||||
| chr11:57717069 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+4262G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717069 | |||||||
| chr11:57717108 | G | A | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+4301G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717108 | |||||||
| chr11:57717176 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.189+4369A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717176 | |||||||
| chr11:57717188 | G | A | 75 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.189+4381G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717188 | |||||||
| chr11:57717263 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+4456C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717263 | |||||||
| chr11:57717458 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189+4651C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717458 | |||||||
| chr11:57717459 | G | C | 1 | a0001c0001t0001g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189+4652G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717459 | |||||||
| chr11:57717529 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+4722C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717529 | |||||||
| chr11:57717640 | C | T | 6 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+4833C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717640 | |||||||
| chr11:57717667 | C | T | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+4860C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717667 | |||||||
| chr11:57717689 | C | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG02622.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.189+4882C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717689 | |||||||
| chr11:57717714 | C | CGAGAGGG others(13): Show |
1 | a0001c0001t0001g0324 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.189+4917_189+4918i others(22): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717714 | ||||||
| chr11:57717717 | G | GAGGGAGA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
59 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.189+4911_189+4917d others(9): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717717 | ||||||
| chr11:57717718 | A | AGGGAGAA others(7): Show |
19 | a0001c0001t0001g0167 a0001c0001t0001g0224 a0001c0001t0001g0306 others(16): Show |
19 | HG00323.hp1 HG00597.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(16): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717718 | A | AGGGAGAA others(20): Show |
1 | a0001c0001t0001g0241 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.189+4917_189+4918i others(29): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717718 | A | AGGGAGAA others(14): Show |
11 | a0001c0001t0001g0106 a0001c0001t0001g0308 a0001c0001t0001g0309 others(8): Show |
11 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(23): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717718 | A | AGGGAGAA others(21): Show |
23 | a0001c0001t0002g0030 a0001c0001t0002g0038 a0001c0001t0002g0055 others(20): Show |
23 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(30): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717718 | A | AGGGAGAA others(28): Show |
5 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(2): Show |
5 | HG01516.hp1 HG01517.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4917_189+4918i others(37): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717718 | A | AGGGAGAA others(35): Show |
2 | a0001c0001t0002g0037 a0001c0001t0002g0077 |
2 | HG02027.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.189+4917_189+4918i others(44): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717718 | A | AGGGAGAA others(42): Show |
2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG01257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.189+4917_189+4918i others(51): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717718 | A | AGGGAGAA others(22): Show |
1 | a0001c0001t0002g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189+4917_189+4918i others(31): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717718 | ||||||
| chr11:57717725 | G | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
202 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.189+4918G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717725 | |||||||
| chr11:57717731 | A | AGGGGAGA others(8): Show |
1 | a0001c0001t0001g0323 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.189+4928_189+4942d others(17): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717731 | ||||||
| chr11:57717746 | G | GGGGAGAG others(14): Show |
1 | a0001c0001t0001g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.189+4952_189+4953i others(23): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | ||||||
| chr11:57717746 | G | GGGGAGAG others(6): Show |
22 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0198 others(19): Show |
22 | HG00544.hp2 HG00735.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(15): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | ||||||
| chr11:57717746 | G | GGGGAGAG others(13): Show |
149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
153 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(22): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | ||||||
| chr11:57717746 | G | GGGGAGAG others(20): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0091 a0001c0001t0001g0092 others(7): Show |
10 | HG01496.hp2 HG02004.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(29): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | ||||||
| chr11:57717746 | G | GGGGAGAG others(27): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
7 | HG03516.hp1 HG03831.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+4948_189+4949i others(36): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | ||||||
| chr11:57717746 | G | GGGGAGAG others(14): Show |
1 | a0001c0001t0001g0032 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(23): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717746 | ||||||
| chr11:57717751 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.189+4944G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717751 | |||||||
| chr11:57717752 | A | AGGGGAGA others(36): Show |
3 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | HG02486.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.189+4948_189+4949i others(45): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717752 | ||||||
| chr11:57717752 | A | AGGGGAGA others(43): Show |
1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(52): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57717752 | ||||||
| chr11:57717755 | G | C | 6 | a0001c0001t0002g0038 a0001c0001t0002g0055 a0001c0001t0002g0056 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+4948G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | |||||||
| chr11:57717755 | G | GGAGAGGG others(25): Show |
1 | a0002c0002t0001g0335 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(34): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | |||||||
| chr11:57717755 | G | GGAGAGGG others(25): Show |
1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+4948_189+4949i others(34): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | |||||||
| chr11:57717755 | G | GGAGAGGG others(24): Show |
1 | a0001c0001t0002g0083 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.189+4948_189+4949i others(33): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717755 | |||||||
| chr11:57717761 | C | G | 2 | a0001c0001t0001g0331 a0001c0001t0003g0110 |
2 | HG02451.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.189+4954C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717761 | |||||||
| chr11:57717767 | C | G | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+4960C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57717767 | |||||||
| chr11:57718016 | T | G | 1 | a0001c0001t0001g0242 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.189+5209T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718016 | |||||||
| chr11:57718297 | C | A | 1 | a0001c0001t0001g0013 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.189+5490C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718297 | |||||||
| chr11:57718298 | A | AT | 156 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(153): Show |
160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.189+5492dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57718298 | ||||||
| chr11:57718298 | A | T | 1 | a0001c0001t0001g0013 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.189+5491A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718298 | |||||||
| chr11:57718300 | A | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+5493A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718300 | |||||||
| chr11:57718330 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189+5523G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718330 | |||||||
| chr11:57718424 | C | T | 3 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 |
3 | HG01516.hp1 HG01517.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.189+5617C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718424 | |||||||
| chr11:57718587 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.189+5780A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718587 | |||||||
| chr11:57718653 | C | CT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0026 others(8): Show |
11 | HG02055.hp1 HG02293.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.189+5866dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57718653 | ||||||
| chr11:57718653 | CT | C | 82 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.189+5866delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57718653 | ||||||
| chr11:57718781 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.189+5974G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718781 | |||||||
| chr11:57718901 | C | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0246 a0001c0001t0001g0300 others(6): Show |
9 | HG00558.hp1 NA18946.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+6094C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57718901 | |||||||
| chr11:57719020 | CAT | C | 13 | a0001c0001t0001g0203 a0001c0001t0001g0298 a0001c0001t0001g0299 others(10): Show |
13 | HG00438.hp1 HG00438.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.189+6226_189+6227d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719020 | ||||||
| chr11:57719020 | CATAT | C | 17 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG01496.hp2 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+6224_189+6227d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719020 | ||||||
| chr11:57719025 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189+6218A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719025 | |||||||
| chr11:57719030 | TATA | T | 46 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0039 others(43): Show |
46 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.189+6224_189+6226d others(5): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719030 | |||||||
| chr11:57719031 | A | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
13 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.189+6224A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719031 | |||||||
| chr11:57719033 | A | AT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0133 a0001c0001t0001g0148 others(9): Show |
12 | HG01175.hp1 HG01346.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.189+6248dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719033 | ||||||
| chr11:57719033 | A | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(26): Show |
30 | HG00438.hp2 HG00642.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.189+6226A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719033 | |||||||
| chr11:57719033 | AT | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(13): Show |
16 | HG00323.hp2 HG00597.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.189+6248delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719033 | ||||||
| chr11:57719033 | ATT | A | 141 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
144 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.189+6247_189+6248d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719033 | ||||||
| chr11:57719035 | T | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0132 others(2): Show |
5 | HG01167.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+6228T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719035 | |||||||
| chr11:57719036 | T | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0224 a0001c0001t0001g0247 others(2): Show |
5 | HG00597.hp2 HG02080.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+6229T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719036 | |||||||
| chr11:57719037 | T | A | 30 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0198 others(27): Show |
30 | HG00544.hp1 HG00544.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.189+6230T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719037 | |||||||
| chr11:57719038 | T | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0224 a0001c0001t0001g0309 |
3 | HG00597.hp2 HG01257.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.189+6231T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719038 | |||||||
| chr11:57719039 | T | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0250 others(2): Show |
5 | HG00735.hp1 HG01099.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+6232T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719039 | |||||||
| chr11:57719040 | T | A | 1 | a0001c0001t0001g0205 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.189+6233T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719040 | |||||||
| chr11:57719179 | G | A | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+6372G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719179 | |||||||
| chr11:57719240 | T | C | 6 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+6433T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719240 | |||||||
| chr11:57719324 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.189+6517C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719324 | |||||||
| chr11:57719514 | C | CT | 81 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0099 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.189+6731dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719514 | ||||||
| chr11:57719514 | C | CTT | 127 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
131 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.189+6730_189+6731d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719514 | ||||||
| chr11:57719514 | C | CTTT | 45 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0022 others(42): Show |
45 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.189+6729_189+6731d others(5): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57719514 | ||||||
| chr11:57719682 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG02015.hp2 NA18964.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.189+6875A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719682 | |||||||
| chr11:57719780 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.189+6973A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57719780 | |||||||
| chr11:57720133 | A | G | 3 | a0001c0001t0003g0108 a0001c0001t0003g0109 a0001c0001t0003g0110 |
3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.189+7326A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720133 | |||||||
| chr11:57720134 | C | CA | 49 | a0001c0001t0001g0100 a0001c0001t0001g0120 a0001c0001t0001g0202 others(46): Show |
49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.189+7346dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | ||||||
| chr11:57720134 | C | CAA | 10 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0039 others(7): Show |
10 | HG00408.hp1 HG00642.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.189+7345_189+7346d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | ||||||
| chr11:57720134 | CA | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
83 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.189+7346delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | ||||||
| chr11:57720134 | CAAAA | C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0246 others(4): Show |
7 | HG01175.hp2 HG02300.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+7343_189+7346d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | ||||||
| chr11:57720134 | CAAAAA | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
154 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.189+7342_189+7346d others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57720134 | ||||||
| chr11:57720202 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.189+7395C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720202 | |||||||
| chr11:57720349 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0151 |
2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.189+7542A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720349 | |||||||
| chr11:57720503 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.189+7696C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720503 | |||||||
| chr11:57720688 | G | A | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.189+7881G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720688 | |||||||
| chr11:57720776 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.189+7969A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720776 | |||||||
| chr11:57720872 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.189+8065A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57720872 | |||||||
| chr11:57721007 | G | GT | 228 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(225): Show |
232 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.189+8214dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721007 | ||||||
| chr11:57721007 | G | GTT | 6 | a0001c0001t0001g0212 a0001c0001t0001g0224 a0001c0001t0001g0288 others(3): Show |
6 | HG00597.hp2 HG02027.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+8213_189+8214d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721007 | ||||||
| chr11:57721099 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.189+8292C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721099 | |||||||
| chr11:57721119 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189+8312C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721119 | |||||||
| chr11:57721131 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.189+8324G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721131 | |||||||
| chr11:57721285 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.189+8478A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721285 | |||||||
| chr11:57721345 | G | GT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0331 others(4): Show |
7 | HG02135.hp2 HG02145.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+8558dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721345 | ||||||
| chr11:57721345 | GT | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.189+8558delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721345 | ||||||
| chr11:57721345 | GTT | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(38): Show |
42 | HG00544.hp2 HG00673.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.189+8557_189+8558d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57721345 | ||||||
| chr11:57721418 | G | A | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.189+8611G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721418 | |||||||
| chr11:57721952 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.189+9145T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57721952 | |||||||
| chr11:57722040 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+9233C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57722040 | |||||||
| chr11:57722232 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02145.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.189+9425G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57722232 | |||||||
| chr11:57722497 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.189+9690A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57722497 | |||||||
| chr11:57723041 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.189+10234G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723041 | |||||||
| chr11:57723072 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.189+10265A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723072 | |||||||
| chr11:57723092 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189+10285T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723092 | |||||||
| chr11:57723106 | G | A | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0260 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+10299G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723106 | |||||||
| chr11:57723115 | AAAAT | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(13): Show |
17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+10324_189+1032 others(8): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723115 | ||||||
| chr11:57723164 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.189+10357A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723164 | |||||||
| chr11:57723278 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.189+10471G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723278 | |||||||
| chr11:57723335 | T | G | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+10528T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723335 | |||||||
| chr11:57723502 | C | CA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0034 others(4): Show |
7 | HG00544.hp2 HG02056.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+10708dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723502 | ||||||
| chr11:57723540 | C | A | 1 | a0001c0001t0002g0081 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.189+10733C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723540 | |||||||
| chr11:57723805 | A | AAAT | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
79 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.189+11028_189+1103 others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723805 | A | AAATAAT | 15 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp1 HG01099.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.189+11025_189+1103 others(10): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723805 | A | AAATAATA others(2): Show |
21 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0118 others(18): Show |
22 | HG01168.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.189+11022_189+1103 others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723805 | A | AAATAATA others(5): Show |
12 | a0001c0001t0002g0030 a0001c0001t0002g0039 a0001c0001t0002g0041 others(9): Show |
12 | HG01069.hp2 HG01071.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.189+11019_189+1103 others(16): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723805 | A | AAATAATA others(8): Show |
37 | a0001c0001t0002g0037 a0001c0001t0002g0040 a0001c0001t0002g0042 others(34): Show |
37 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.189+11016_189+1103 others(19): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723805 | A | AAATAATA others(11): Show |
5 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0059 others(2): Show |
5 | HG02683.hp2 HG03834.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+11013_189+1103 others(22): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723805 | A | AAATAATA others(14): Show |
1 | a0001c0001t0002g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.189+11010_189+1103 others(25): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723805 | AAATAATA others(8): Show |
A | 1 | a0001c0001t0001g0157 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.189+11016_189+1103 others(19): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57723805 | ||||||
| chr11:57723899 | T | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.189+11092T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723899 | |||||||
| chr11:57723900 | T | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
106 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.189+11093T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723900 | |||||||
| chr11:57723968 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.189+11161A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57723968 | |||||||
| chr11:57724019 | G | A | 4 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02647.hp1 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+11212G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724019 | |||||||
| chr11:57724021 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0296 |
2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.189+11214A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724021 | |||||||
| chr11:57724647 | T | TA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0118 others(5): Show |
9 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+11845dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57724647 | ||||||
| chr11:57724697 | C | A | 1 | a0001c0001t0002g0049 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189+11890C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724697 | |||||||
| chr11:57724754 | A | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.189+11947A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57724754 | |||||||
| chr11:57725012 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.189+12205C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725012 | |||||||
| chr11:57725038 | C | CA | 24 | a0001c0001t0001g0033 a0001c0001t0001g0115 a0001c0001t0001g0133 others(21): Show |
24 | HG00733.hp1 HG01192.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.189+12248dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57725038 | ||||||
| chr11:57725052 | A | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(13): Show |
17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.189+12245A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725052 | |||||||
| chr11:57725056 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0285 |
2 | NA18985.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.189+12249G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725056 | |||||||
| chr11:57725057 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.189+12250A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725057 | |||||||
| chr11:57725666 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190-11942G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725666 | |||||||
| chr11:57725765 | C | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.190-11843C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725765 | |||||||
| chr11:57725785 | GTAC | G | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-11820_190-1181 others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57725785 | ||||||
| chr11:57725923 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.190-11685A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57725923 | |||||||
| chr11:57726024 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.190-11584A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726024 | |||||||
| chr11:57726150 | C | A | 51 | a0001c0001t0002g0030 a0001c0001t0002g0038 a0001c0001t0002g0039 others(48): Show |
51 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.190-11458C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726150 | |||||||
| chr11:57726285 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190-11323C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726285 | |||||||
| chr11:57726338 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(13): Show |
17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-11270G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726338 | |||||||
| chr11:57726726 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.190-10882T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57726726 | |||||||
| chr11:57727015 | A | C | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-10593A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727015 | |||||||
| chr11:57727038 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.190-10570T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727038 | |||||||
| chr11:57727562 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0026 |
2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.190-10046T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727562 | |||||||
| chr11:57727765 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.190-9843G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57727765 | |||||||
| chr11:57728014 | TTTGA | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(20): Show |
24 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.190-9588_190-9585d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57728014 | ||||||
| chr11:57728169 | C | CT | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(72): Show |
79 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.190-9428dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57728169 | ||||||
| chr11:57728174 | T | G | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-9434T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728174 | |||||||
| chr11:57728202 | G | A | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-9406G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728202 | |||||||
| chr11:57728414 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0144 others(5): Show |
9 | HG00621.hp1 HG02015.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-9194C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728414 | |||||||
| chr11:57728681 | C | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(3): Show |
6 | HG03831.hp2 NA18961.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-8927C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728681 | |||||||
| chr11:57728713 | A | C | 1 | a0001c0001t0003g0127 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.190-8895A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57728713 | |||||||
| chr11:57728733 | CAT | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG02622.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.190-8873_190-8872d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57728733 | ||||||
| chr11:57729018 | C | T | 7 | a0001c0001t0001g0232 a0001c0001t0001g0245 a0001c0001t0001g0284 others(4): Show |
7 | HG00733.hp2 HG01192.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-8590C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729018 | |||||||
| chr11:57729168 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.190-8440A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729168 | |||||||
| chr11:57729348 | C | T | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-8260C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729348 | |||||||
| chr11:57729363 | G | C | 1 | a0001c0001t0001g0006 | 2 | NA18970.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.190-8245G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729363 | |||||||
| chr11:57729539 | C | A | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-8069C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729539 | |||||||
| chr11:57729541 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0157 |
2 | HG00642.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.190-8067C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729541 | |||||||
| chr11:57729838 | T | C | 1 | a0001c0001t0009g0015 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.190-7770T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729838 | |||||||
| chr11:57729934 | C | A | 1 | a0001c0001t0002g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.190-7674C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729934 | |||||||
| chr11:57729937 | G | A | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-7671G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729937 | |||||||
| chr11:57729972 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0283 |
2 | NA18991.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.190-7636G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57729972 | |||||||
| chr11:57730041 | T | C | 7 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(4): Show |
7 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-7567T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730041 | |||||||
| chr11:57730108 | C | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-7500C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730108 | |||||||
| chr11:57730123 | T | TTA | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(39): Show |
46 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.190-7471_190-7470d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730123 | ||||||
| chr11:57730131 | A | G | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-7477A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730131 | |||||||
| chr11:57730298 | G | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG01175.hp1 HG01515.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.190-7310G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730298 | |||||||
| chr11:57730324 | G | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG01261.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-7284G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730324 | |||||||
| chr11:57730375 | C | T | 57 | a0001c0001t0002g0030 a0001c0001t0002g0037 a0001c0001t0002g0038 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-7233C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730375 | |||||||
| chr11:57730426 | T | TA | 9 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0100 others(6): Show |
9 | HG00639.hp2 HG01106.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-7154dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730426 | ||||||
| chr11:57730426 | TA | T | 159 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(156): Show |
163 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.190-7154delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730426 | ||||||
| chr11:57730426 | TAA | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(65): Show |
73 | HG00140.hp1 HG00544.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.190-7155_190-7154d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730426 | ||||||
| chr11:57730468 | G | A | 38 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(35): Show |
38 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.190-7140G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730468 | |||||||
| chr11:57730508 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.190-7100G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730508 | |||||||
| chr11:57730652 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.190-6956C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730652 | |||||||
| chr11:57730760 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
269 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(266): Show |
intron_variant | MODIFIER | c.190-6848C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730760 | |||||||
| chr11:57730834 | A | G | 8 | a0001c0001t0002g0040 a0001c0001t0002g0042 a0001c0001t0002g0043 others(5): Show |
8 | HG00323.hp1 HG00741.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-6774A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730834 | |||||||
| chr11:57730857 | A | G | 3 | a0001c0001t0003g0108 a0001c0001t0003g0109 a0001c0001t0003g0110 |
3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.190-6751A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57730857 | |||||||
| chr11:57730988 | C | CTTAAA | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
270 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.190-6617_190-6616i others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57730988 | ||||||
| chr11:57731109 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.190-6499C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731109 | |||||||
| chr11:57731111 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0305 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.190-6497G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731111 | |||||||
| chr11:57731125 | G | T | 3 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0045 |
3 | HG00741.hp2 HG01167.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.190-6483G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731125 | |||||||
| chr11:57731125 | GTTTT | G | 38 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
39 | HG00438.hp1 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.190-6458_190-6455d others(6): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | ||||||
| chr11:57731125 | GTTTTT | G | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
115 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.190-6459_190-6455d others(7): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | ||||||
| chr11:57731125 | GTTTTTT | G | 11 | a0001c0001t0001g0133 a0001c0001t0001g0175 a0001c0001t0001g0176 others(8): Show |
11 | HG01361.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.190-6460_190-6455d others(8): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | ||||||
| chr11:57731125 | GTTTTTTT | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0128 a0001c0001t0001g0134 others(14): Show |
18 | HG00621.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.190-6461_190-6455d others(9): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | ||||||
| chr11:57731125 | GTTTTTTT others(1): Show |
G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(61): Show |
67 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.190-6462_190-6455d others(10): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | ||||||
| chr11:57731125 | GTTTTTTT others(2): Show |
G | 18 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0112 others(15): Show |
19 | HG01261.hp2 HG02451.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-6463_190-6455d others(11): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731125 | ||||||
| chr11:57731133 | T | TTG | 9 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0043 others(6): Show |
9 | HG00741.hp2 HG01069.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-6474_190-6473i others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731133 | ||||||
| chr11:57731134 | T | TG | 45 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0002g0030 others(42): Show |
45 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.190-6474_190-6473i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731134 | |||||||
| chr11:57731135 | T | G | 13 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(10): Show |
13 | HG01496.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.190-6473T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731135 | |||||||
| chr11:57731136 | T | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0294 |
2 | NA18976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.190-6472T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731136 | |||||||
| chr11:57731137 | T | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0026 others(1): Show |
4 | NA18947.hp1 NA18960.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-6471T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731137 | |||||||
| chr11:57731139 | T | G | 5 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
5 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-6469T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731139 | |||||||
| chr11:57731140 | T | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG00544.hp2 HG02056.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.190-6468T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731140 | |||||||
| chr11:57731141 | T | G | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-6467T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731141 | |||||||
| chr11:57731142 | T | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0276 |
2 | HG02683.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.190-6466T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731142 | |||||||
| chr11:57731144 | T | G | 1 | a0001c0001t0001g0006 | 2 | NA18970.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.190-6464T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731144 | |||||||
| chr11:57731237 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.190-6371G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731237 | |||||||
| chr11:57731433 | C | CT | 130 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(127): Show |
132 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.190-6151dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731433 | ||||||
| chr11:57731433 | C | CTT | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(92): Show |
97 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.190-6152_190-6151d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731433 | ||||||
| chr11:57731433 | CT | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
15 | HG01261.hp2 HG02273.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.190-6151delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57731433 | ||||||
| chr11:57731442 | T | TC | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0260 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-6166_190-6165i others(3): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731442 | |||||||
| chr11:57731593 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
269 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(266): Show |
intron_variant | MODIFIER | c.190-6015C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731593 | |||||||
| chr11:57731726 | G | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.190-5882G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731726 | |||||||
| chr11:57731786 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.190-5822C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57731786 | |||||||
| chr11:57732000 | CAT | C | 3 | a0001c0001t0003g0108 a0001c0001t0003g0109 a0001c0001t0003g0110 |
3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.190-5605_190-5604d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57732000 | ||||||
| chr11:57732167 | A | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0319 |
2 | NA18950.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.190-5441A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732167 | |||||||
| chr11:57732183 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
108 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.190-5425T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732183 | |||||||
| chr11:57732251 | CTG | C | 3 | a0001c0001t0003g0108 a0001c0001t0003g0109 a0001c0001t0003g0110 |
3 | HG02451.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.190-5354_190-5353d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57732251 | ||||||
| chr11:57732494 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-5114A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732494 | |||||||
| chr11:57732607 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.190-5001A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732607 | |||||||
| chr11:57732661 | C | T | 2 | a0001c0001t0001g0275 a0001c0001t0001g0294 |
2 | NA18976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.190-4947C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732661 | |||||||
| chr11:57732662 | A | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-4946A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732662 | |||||||
| chr11:57732702 | T | G | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190-4906T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732702 | |||||||
| chr11:57732813 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.190-4795A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732813 | |||||||
| chr11:57732820 | G | T | 1 | a0001c0001t0001g0291 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.190-4788G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732820 | |||||||
| chr11:57732870 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.190-4738G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732870 | |||||||
| chr11:57732890 | T | G | 3 | a0001c0001t0002g0050 a0001c0001t0002g0064 a0001c0001t0002g0066 |
3 | HG01070.hp1 HG01081.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.190-4718T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732890 | |||||||
| chr11:57732927 | T | C | 6 | a0001c0001t0002g0030 a0001c0001t0002g0061 a0001c0001t0002g0062 others(3): Show |
6 | HG02129.hp1 HG02602.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-4681T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732927 | |||||||
| chr11:57732978 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.190-4630G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57732978 | |||||||
| chr11:57733056 | C | A | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.190-4552C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733056 | |||||||
| chr11:57733115 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.190-4493T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733115 | |||||||
| chr11:57733238 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.190-4370C>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733238 | |||||||
| chr11:57733247 | A | AT | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0021 others(36): Show |
39 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.190-4336dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | ||||||
| chr11:57733247 | AT | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
101 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.190-4336delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | ||||||
| chr11:57733247 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.190-4345_190-4336d others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | ||||||
| chr11:57733247 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0287 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.190-4346_190-4336d others(13): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57733247 | ||||||
| chr11:57733348 | C | T | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-4260C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733348 | |||||||
| chr11:57733447 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-4161G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733447 | |||||||
| chr11:57733548 | C | T | 6 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-4060C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733548 | |||||||
| chr11:57733694 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-3914G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733694 | |||||||
| chr11:57733710 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
107 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.190-3898C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733710 | |||||||
| chr11:57733748 | T | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.190-3860T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57733748 | |||||||
| chr11:57734067 | G | A | 3 | a0001c0001t0001g0307 a0001c0001t0001g0310 a0001c0001t0001g0323 |
3 | NA18973.hp2 NA19056.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.190-3541G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734067 | |||||||
| chr11:57734157 | C | CA | 12 | a0001c0001t0001g0104 a0001c0001t0001g0168 a0001c0001t0001g0172 others(9): Show |
12 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.190-3421dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | C | CAA | 7 | a0001c0001t0001g0113 a0001c0001t0001g0165 a0001c0001t0002g0043 others(4): Show |
7 | HG00741.hp2 HG01192.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-3422_190-3421d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | CA | C | 120 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0024 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.190-3421delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | CAA | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
135 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.190-3422_190-3421d others(4): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | CAAA | C | 6 | a0001c0001t0001g0235 a0001c0001t0001g0254 a0001c0001t0001g0271 others(3): Show |
6 | HG00738.hp1 HG01168.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-3423_190-3421d others(5): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0280 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.190-3430_190-3421d others(12): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-3433_190-3421d others(15): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | CAAAAAAA others(7): Show |
C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0117 others(13): Show |
17 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-3434_190-3421d others(16): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734157 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0147 |
2 | HG01891.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.190-3435_190-3421d others(17): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734157 | ||||||
| chr11:57734282 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.190-3326T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734282 | |||||||
| chr11:57734442 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0294 |
2 | NA18976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.190-3166A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734442 | |||||||
| chr11:57734466 | A | C | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.190-3142A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734466 | |||||||
| chr11:57734815 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.190-2793A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734815 | |||||||
| chr11:57734825 | AC | A | 5 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(2): Show |
5 | HG00408.hp1 HG00438.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-2781delC | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57734825 | ||||||
| chr11:57734920 | G | A | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.190-2688G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734920 | |||||||
| chr11:57734953 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.190-2655G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57734953 | |||||||
| chr11:57735160 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0118 others(5): Show |
9 | HG02451.hp1 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-2448G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735160 | |||||||
| chr11:57735209 | T | G | 1 | a0001c0001t0001g0330 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.190-2399T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735209 | |||||||
| chr11:57735277 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.190-2331C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735277 | |||||||
| chr11:57735385 | A | G | 1 | a0001c0001t0001g0314 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.190-2223A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735385 | |||||||
| chr11:57735483 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.190-2125T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735483 | |||||||
| chr11:57735506 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.190-2102C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735506 | |||||||
| chr11:57735735 | A | G | 1 | a0001c0003t0010g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190-1873A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735735 | |||||||
| chr11:57735745 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.190-1863A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735745 | |||||||
| chr11:57735767 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.190-1841G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735767 | |||||||
| chr11:57735789 | G | A | 6 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(3): Show |
6 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-1819G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735789 | |||||||
| chr11:57735794 | G | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
78 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.190-1814G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57735794 | |||||||
| chr11:57736053 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.190-1555T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736053 | |||||||
| chr11:57736108 | A | G | 1 | a0001c0001t0012g0216 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.190-1500A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736108 | |||||||
| chr11:57736142 | T | G | 3 | a0001c0001t0002g0062 a0001c0001t0002g0089 a0001c0001t0006g0088 |
3 | HG02129.hp1 HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.190-1466T>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736142 | |||||||
| chr11:57736212 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.190-1396C>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736212 | |||||||
| chr11:57736340 | TA | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
320 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.190-1253delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57736340 | ||||||
| chr11:57736342 | A | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.190-1266A>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736342 | |||||||
| chr11:57736481 | G | GT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG00621.hp1 NA18976.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-1126dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57736481 | ||||||
| chr11:57736539 | A | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.190-1069A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736539 | |||||||
| chr11:57736602 | T | C | 5 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | NA18945.hp2 NA18950.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-1006T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736602 | |||||||
| chr11:57736658 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.190-950C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736658 | |||||||
| chr11:57736752 | G | C | 7 | a0001c0001t0001g0232 a0001c0001t0001g0245 a0001c0001t0001g0284 others(4): Show |
7 | HG00733.hp2 HG01192.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.190-856G>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736752 | |||||||
| chr11:57736776 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.190-832T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736776 | |||||||
| chr11:57736807 | G | T | 1 | a0001c0001t0001g0280 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.190-801G>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736807 | |||||||
| chr11:57736883 | C | CA | 12 | a0001c0001t0001g0036 a0001c0001t0001g0233 a0001c0001t0001g0246 others(9): Show |
12 | HG00558.hp1 HG01257.hp2 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.190-709dupA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 57736883 | ||||||
| chr11:57736905 | CAT | C | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0260 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-702_190-701del others(2): Show |
TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57736905 | |||||||
| chr11:57737006 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA19009.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.190-602C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57737006 | |||||||
| chr11:57737061 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.190-547A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57737061 | |||||||
| chr11:57737489 | T | C | 5 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | NA18945.hp2 NA18950.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-119T>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 1/7 | chr11 | 57737489 | |||||||
| chr11:57737750 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250+82A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 2/7 | chr11 | 57737750 | |||||||
| chr11:57738048 | C | CT | 6 | a0001c0001t0002g0037 a0001c0001t0002g0048 a0001c0001t0002g0053 others(3): Show |
6 | HG02027.hp1 NA19002.hp2 NA19064.hp1 others(3): Show |
intron_variant | MODIFIER | c.364+35dupT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 57738048 | ||||||
| chr11:57738048 | CT | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0180 a0001c0001t0001g0191 others(8): Show |
11 | HG01261.hp2 HG03139.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.364+35delT | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 57738048 | ||||||
| chr11:57738116 | T | A | 1 | a0001c0001t0002g0081 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.364+90T>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 3/7 | chr11 | 57738116 | |||||||
| chr11:57738475 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.441+45G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 4/7 | chr11 | 57738475 | |||||||
| chr11:57739431 | A | C | 18 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0232 others(15): Show |
18 | HG00597.hp1 HG00733.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.744+171A>C | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739431 | |||||||
| chr11:57739500 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.744+240G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739500 | |||||||
| chr11:57739613 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.744+353C>T | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739613 | |||||||
| chr11:57739672 | G | A | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
161 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.744+412G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739672 | |||||||
| chr11:57739754 | GA | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0118 others(7): Show |
11 | HG02451.hp1 HG02486.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.745-332delA | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 57739754 | ||||||
| chr11:57739841 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.745-258A>G | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739841 | |||||||
| chr11:57739979 | G | A | 7 | a0001c0001t0001g0236 a0001c0001t0001g0248 a0001c0001t0001g0249 others(4): Show |
7 | HG00735.hp1 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.745-120G>A | TMX2 | ENSG00000213593.10 | transcript | ENST00000278422.9 | protein_coding | 7/7 | chr11 | 57739979 |