Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9968 |
| ensemblid | ENSG00000184634.17 |
| hgncid | 11957 |
| symbol | MED12 |
| name | mediator complex subunit 12 |
| refseq_nuc | NM_005120.3 |
| refseq_prot | NP_005111.2 |
| ensembl_nuc | ENST00000374080.8 |
| ensembl_prot | ENSP00000363193.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 71118596 |
| end | 71142450 |
| strand | + |
| ver | v1.2 |
| region | chrX:71118596-71142450 |
| region5000 | chrX:71113596-71147450 |
| regionname0 | MED12_chrX_71118596_71142450 |
| regionname5000 | MED12_chrX_71113596_71147450 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 2177 | 263 | 77 | 51 | 100 | 6 | 27 | 77 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2172): Show |
chrX | 71113596 | 71147450 |
| a0002 | 0/0 | 2181 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2176): Show |
chrX | 71113596 | 71147450 |
| a0003 | 0/0 | 2177 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2172): Show |
chrX | 71113596 | 71147450 |
| a0004 | 0/0 | 2177 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2172): Show |
chrX | 71113596 | 71147450 |
| a0005 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2172): Show |
chrX | 71113596 | 71147450 |
| a0006 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2172): Show |
chrX | 71113596 | 71147450 |
| a0007 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2172): Show |
chrX | 71113596 | 71147450 |
| a0008 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | MAAFG others(2172): Show |
chrX | 71113596 | 71147450 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 6531 | 218 | 61 | 34 | 93 | 3 | 26 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0002 | 0/1 | 6531 | 16 | 0 | 10 | 1 | 3 | 1 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0003 | 0/0 | 6531 | 10 | 1 | 6 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0004 | 0/0 | 6531 | 8 | 8 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0006 | 0/0 | 6531 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0008 | 0/0 | 6531 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0009 | 0/0 | 6531 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0011 | 0/0 | 6531 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0013 | 0/0 | 6531 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0014 | 0/0 | 6531 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0017 | 0/0 | 6531 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0018 | 0/0 | 6531 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0001c0020 | 0/0 | 6531 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0002c0005 | 0/0 | 6543 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6538): Show |
chrX | 71113596 | 71147450 | ||
| a0003c0007 | 0/0 | 6531 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0004c0019 | 0/0 | 6531 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0005c0012 | 0/0 | 6531 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0006c0015 | 0/0 | 6531 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0007c0016 | 0/0 | 6531 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 | ||
| a0008c0010 | 0/0 | 6531 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | ATGGC others(6526): Show |
chrX | 71113596 | 71147450 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6925 | 218 | 61 | 34 | 93 | 3 | 26 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0002t0001 | 0/1 | 6925 | 16 | 0 | 10 | 1 | 3 | 1 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0003t0001 | 0/0 | 6925 | 10 | 1 | 6 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0004t0001 | 0/0 | 6925 | 8 | 8 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0006t0001 | 0/0 | 6925 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0008t0001 | 0/0 | 6925 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0009t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0011t0001 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0013t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0014t0001 | 0/0 | 6925 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0017t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0018t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0001c0020t0001 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0002c0005t0001 | 0/0 | 6937 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6932): Show |
chrX | 71113596 | 71147450 |
| a0003c0007t0001 | 0/0 | 6925 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0004c0019t0001 | 0/0 | 6925 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0005c0012t0001 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0006c0015t0001 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0007c0016t0001 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| a0008c0010t0001 | 0/0 | 6925 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | AGTTT others(6920): Show |
chrX | 71113596 | 71147450 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 12 | 0 | 0 | 8 | 0 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0002 | 0/0 | 15 | 8 | 1 | 3 | 0 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 2 | 2 | 1 | 3 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0005 | 0/0 | 11 | 2 | 0 | 7 | 0 | 2 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0006 | 0/0 | 11 | 1 | 5 | 4 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 1 | 2 | 0 | 2 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0013 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0018 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0002t0001g0007 | 0/0 | 8 | 0 | 6 | 0 | 1 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0002t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0002t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0003t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0003t0001g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0004t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0008t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0009t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0011t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0013t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0014t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0017t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0018t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0001c0020t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0002c0005t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0002c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0003c0007t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0003c0007t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0004c0019t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0005c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0006c0015t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0007c0016t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| a0008c0010t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | GBR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00738 | hp1 | a0001 | c0014 | t0001 | g0043 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01257 | hp1 | a0003 | c0007 | t0001 | g0005 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01258 | hp1 | a0003 | c0007 | t0001 | g0108 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01884 | hp2 | a0001 | c0008 | t0001 | g0036 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0068 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02615 | hp2 | a0001 | c0013 | t0001 | g0131 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02630 | hp1 | a0001 | c0018 | t0001 | g0130 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02630 | hp2 | a0002 | c0005 | t0001 | g0007 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02818 | hp2 | a0001 | c0008 | t0001 | g0036 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0042 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02886 | hp2 | a0001 | c0017 | t0001 | g0128 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0041 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03516 | hp1 | a0001 | c0020 | t0001 | g0002 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0012 | AFR | GWD | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03579 | hp1 | a0002 | c0005 | t0001 | g0007 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03669 | hp2 | a0004 | c0019 | t0001 | g0011 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18940 | hp1 | a0005 | c0012 | t0001 | g0075 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18979 | hp1 | a0006 | c0015 | t0001 | g0055 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18988 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19001 | hp2 | a0007 | c0016 | t0001 | g0113 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19030 | hp2 | a0001 | c0009 | t0001 | g0044 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19056 | hp1 | a0001 | c0011 | t0001 | g0117 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19059 | hp2 | a0008 | c0010 | t0001 | g0077 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19088 | hp1 | a0001 | c0006 | t0001 | g0058 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ASW | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0136 | EUR | TSI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | TSI | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | USA | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA21309 | hp1 | a0002 | c0005 | t0001 | g0133 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0135 | REF | REF | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | MED12_chrX_71113596_71147450 | MED12 | chrX | 71113596 | 71147450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71122793 | T | A | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.1404T>A | p.Phe468Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/45 | 1563/6925 | 1404/6534 | 468/2177 | chrX | 71122793 | |||
| chrX:71124213 | T | A | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1799T>A | p.Phe600Tyr | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1958/6925 | 1799/6534 | 600/2177 | chrX | 71124213 | |||
| chrX:71124215 | T | A | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1801T>A | p.Cys601Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1960/6925 | 1801/6534 | 601/2177 | chrX | 71124215 | |||
| chrX:71124224 | A | T | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1810A>T | p.Ile604Phe | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1969/6925 | 1810/6534 | 604/2177 | chrX | 71124224 | |||
| chrX:71125060 | C | T | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2140C>T | p.Pro714Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2299/6925 | 2140/6534 | 714/2177 | chrX | 71125060 | |||
| chrX:71125061 | C | A | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2141C>A | p.Pro714His | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2300/6925 | 2141/6534 | 714/2177 | chrX | 71125061 | |||
| chrX:71125064 | A | T | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2144A>T | p.Lys715Met | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2303/6925 | 2144/6534 | 715/2177 | chrX | 71125064 | |||
| chrX:71125067 | A | T | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2147A>T | p.Glu716Val | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2306/6925 | 2147/6534 | 716/2177 | chrX | 71125067 | |||
| chrX:71125070 | A | T | 1 | a0005 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2150A>T | p.Lys717Met | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2309/6925 | 2150/6534 | 717/2177 | chrX | 71125070 | |||
| chrX:71126084 | C | T | 1 | a0004 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2471C>T | p.Pro824Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 18/45 | 2630/6925 | 2471/6534 | 824/2177 | chrX | 71126084 | |||
| chrX:71132900 | G | A | 1 | a0006 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.4471G>A | p.Gly1491Arg | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 32/45 | 4630/6925 | 4471/6534 | 1491/2177 | chrX | 71132900 | |||
| chrX:71135170 | G | T | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.4942G>T | p.Val1648Phe | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/45 | 5101/6925 | 4942/6534 | 1648/2177 | chrX | 71135170 | |||
| chrX:71136510 | C | T | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5255C>T | p.Pro1752Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5414/6925 | 5255/6534 | 1752/2177 | chrX | 71136510 | |||
| chrX:71136512 | G | C | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5257G>C | p.Ala1753Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5416/6925 | 5257/6534 | 1753/2177 | chrX | 71136512 | |||
| chrX:71136522 | T | C | 1 | a0003 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.5267T>C | p.Leu1756Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5426/6925 | 5267/6534 | 1756/2177 | chrX | 71136522 | |||
| chrX:71137828 | C | A | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5929C>A | p.His1977Asn | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/45 | 6088/6925 | 5929/6534 | 1977/2177 | chrX | 71137828 | |||
| chrX:71137829 | A | C | 1 | a0008 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.5930A>C | p.His1977Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/45 | 6089/6925 | 5930/6534 | 1977/2177 | chrX | 71137829 | |||
| chrX:71141278 | C | A | 1 | a0007 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.6316C>A | p.Gln2106Lys | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/45 | 6475/6925 | 6316/6534 | 2106/2177 | chrX | 71141278 | |||
| chrX:71141301 | A | ACAGCAAC others(5): Show |
1 | a0002 | 3 | HG02630.hp2 HG03579.hp1 NA21309.hp1 |
disruptive_inframe_insertion | MODERATE | c.6348_6359dupCCAGCA others(6): Show |
p.His2116_Gln2119dup | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/45 | 6519/6925 | 6360/6534 | 2120/2177 | INFO_REALIGN_3_PRIME | chrX | 71141301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71119862 | G | A | 1 | a0001c0009 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.381G>A | p.Thr127Thr | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 3/45 | 540/6925 | 381/6534 | 127/2177 | chrX | 71119862 | |||
| chrX:71119865 | A | G | 1 | a0001c0020 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.384A>G | p.Gln128Gln | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 3/45 | 543/6925 | 384/6534 | 128/2177 | chrX | 71119865 | |||
| chrX:71122775 | G | T | 1 | a0001c0008 | 2 | HG01884.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.1386G>T | p.Val462Val | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/45 | 1545/6925 | 1386/6534 | 462/2177 | chrX | 71122775 | |||
| chrX:71123671 | T | A | 1 | a0001c0011 | 1 | NA19056.hp1 | synonymous_variant | LOW | c.1695T>A | p.Ile565Ile | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 12/45 | 1854/6925 | 1695/6534 | 565/2177 | chrX | 71123671 | |||
| chrX:71124211 | G | A | 1 | a0005c0012 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.1797G>A | p.Leu599Leu | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/45 | 1956/6925 | 1797/6534 | 599/2177 | chrX | 71124211 | |||
| chrX:71125065 | G | A | 1 | a0005c0012 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.2145G>A | p.Lys715Lys | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/45 | 2304/6925 | 2145/6534 | 715/2177 | chrX | 71125065 | |||
| chrX:71125383 | G | A | 1 | a0001c0004 | 8 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
synonymous_variant | LOW | c.2259G>A | p.Arg753Arg | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 16/45 | 2418/6925 | 2259/6534 | 753/2177 | chrX | 71125383 | |||
| chrX:71126412 | G | A | 1 | a0001c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.2613G>A | p.Gln871Gln | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/45 | 2772/6925 | 2613/6534 | 871/2177 | chrX | 71126412 | |||
| chrX:71126430 | C | T | 1 | a0001c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.2631C>T | p.Phe877Phe | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/45 | 2790/6925 | 2631/6534 | 877/2177 | chrX | 71126430 | |||
| chrX:71127372 | C | T | 2 | a0001c0013 a0001c0018 |
2 | HG02615.hp2 HG02630.hp1 |
synonymous_variant | LOW | c.2886C>T | p.Ser962Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 21/45 | 3045/6925 | 2886/6534 | 962/2177 | chrX | 71127372 | |||
| chrX:71128600 | C | T | 1 | a0001c0017 | 1 | HG02886.hp2 | splice_region_variant&synonymous_variant | LOW | c.3357C>T | p.Val1119Val | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 24/45 | 3516/6925 | 3357/6534 | 1119/2177 | chrX | 71128600 | |||
| chrX:71129687 | G | A | 2 | a0001c0009 a0001c0014 |
2 | HG00738.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.3699G>A | p.Ala1233Ala | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 27/45 | 3858/6925 | 3699/6534 | 1233/2177 | chrX | 71129687 | |||
| chrX:71130097 | A | C | 3 | a0001c0002 a0002c0005 a0004c0019 |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
synonymous_variant | LOW | c.3930A>C | p.Pro1310Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/45 | 4089/6925 | 3930/6534 | 1310/2177 | chrX | 71130097 | |||
| chrX:71130109 | T | C | 1 | a0001c0006 | 2 | NA18988.hp1 NA19088.hp1 |
synonymous_variant | LOW | c.3942T>C | p.Ser1314Ser | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/45 | 4101/6925 | 3942/6534 | 1314/2177 | chrX | 71130109 | |||
| chrX:71136511 | T | G | 1 | a0008c0010 | 1 | NA19059.hp2 | synonymous_variant | LOW | c.5256T>G | p.Pro1752Pro | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/45 | 5415/6925 | 5256/6534 | 1752/2177 | chrX | 71136511 | |||
| chrX:71137013 | C | T | 1 | a0001c0003 | 10 | HG00609.hp1 HG01257.hp2 HG01496.hp2 others(7): Show |
synonymous_variant | LOW | c.5535C>T | p.Asn1845Asn | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 38/45 | 5694/6925 | 5535/6534 | 1845/2177 | chrX | 71137013 | |||
| chrX:71137602 | T | A | 1 | a0008c0010 | 1 | NA19059.hp2 | synonymous_variant | LOW | c.5793T>A | p.Thr1931Thr | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 40/45 | 5952/6925 | 5793/6534 | 1931/2177 | chrX | 71137602 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71119214 | C | A | 1 | a0001c0001t0001g0037 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.100-159C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | chrX | 71119214 | |||||||
| chrX:71119309 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
6 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-64A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 1/44 | chrX | 71119309 | |||||||
| chrX:71119535 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0038 |
3 | HG00099.hp2 HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.204+58G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 2/44 | chrX | 71119535 | |||||||
| chrX:71119648 | C | T | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-38C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 2/44 | chrX | 71119648 | |||||||
| chrX:71119975 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.397-39G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 3/44 | chrX | 71119975 | |||||||
| chrX:71120388 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.553+218G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120388 | |||||||
| chrX:71120472 | C | G | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.553+302C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120472 | |||||||
| chrX:71120536 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.553+366T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120536 | |||||||
| chrX:71120609 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.554-362A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120609 | |||||||
| chrX:71120615 | A | AT | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.554-343dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | INFO_REALIGN_3_PRIME | chrX | 71120615 | ||||||
| chrX:71120888 | A | G | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(48): Show |
99 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.554-83A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120888 | |||||||
| chrX:71120950 | C | A | 4 | a0001c0004t0001g0012 a0001c0004t0001g0021 a0001c0004t0001g0041 others(1): Show |
8 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.554-21C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 4/44 | chrX | 71120950 | |||||||
| chrX:71121272 | T | TACTTTAT others(7): Show |
8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.736-53_736-40dupCT others(12): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chrX | 71121272 | ||||||
| chrX:71121319 | A | C | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.736-8A>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 5/44 | chrX | 71121319 | |||||||
| chrX:71121843 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1101+27C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | chrX | 71121843 | |||||||
| chrX:71122064 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(37): Show |
77 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.1102-136G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | chrX | 71122064 | |||||||
| chrX:71122179 | T | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0129 a0001c0004t0001g0012 others(5): Show |
12 | HG00738.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1102-21T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 7/44 | chrX | 71122179 | |||||||
| chrX:71122386 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1248+40A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/44 | chrX | 71122386 | |||||||
| chrX:71122424 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1248+78G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 8/44 | chrX | 71122424 | |||||||
| chrX:71122691 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1349-47T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 9/44 | chrX | 71122691 | |||||||
| chrX:71122970 | A | G | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1485+96A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 10/44 | chrX | 71122970 | |||||||
| chrX:71123343 | A | G | 2 | a0001c0013t0001g0131 a0001c0018t0001g0130 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1617+117A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 11/44 | chrX | 71123343 | |||||||
| chrX:71123771 | A | G | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1744+51A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 12/44 | chrX | 71123771 | |||||||
| chrX:71124481 | G | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(48): Show |
99 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1974+93G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/44 | chrX | 71124481 | |||||||
| chrX:71124482 | AG | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
8 | HG01243.hp1 HG01255.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1974+100delG | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 13/44 | INFO_REALIGN_3_PRIME | chrX | 71124482 | ||||||
| chrX:71124913 | G | T | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.2056-63G>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 14/44 | chrX | 71124913 | |||||||
| chrX:71125235 | A | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2226+89A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 15/44 | chrX | 71125235 | |||||||
| chrX:71125743 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(15): Show |
35 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.2422+30C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | chrX | 71125743 | |||||||
| chrX:71125833 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2422+120T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | chrX | 71125833 | |||||||
| chrX:71125833 | T | G | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.2422+120T>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 17/44 | chrX | 71125833 | |||||||
| chrX:71126590 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG00423.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2685+106A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 19/44 | chrX | 71126590 | |||||||
| chrX:71127309 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2850-27C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 20/44 | chrX | 71127309 | |||||||
| chrX:71127611 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2981+144G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 21/44 | chrX | 71127611 | |||||||
| chrX:71128467 | G | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
44 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.3354+27G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 23/44 | chrX | 71128467 | |||||||
| chrX:71128494 | G | A | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.3354+54G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 23/44 | chrX | 71128494 | |||||||
| chrX:71128584 | G | T | 1 | a0001c0017t0001g0128 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3355-14G>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 23/44 | chrX | 71128584 | |||||||
| chrX:71128770 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3475+52C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 24/44 | chrX | 71128770 | |||||||
| chrX:71129658 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
8 | HG01243.hp1 HG01255.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3692-22A>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 26/44 | chrX | 71129658 | |||||||
| chrX:71129877 | C | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0082 a0001c0001t0001g0083 |
4 | NA18979.hp2 NA19070.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.3867+22C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 27/44 | chrX | 71129877 | |||||||
| chrX:71130437 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0034 others(9): Show |
19 | HG00423.hp2 HG00735.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.4047+223A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | chrX | 71130437 | |||||||
| chrX:71130748 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0105 a0001c0001t0001g0106 |
4 | HG01109.hp1 HG01934.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.4047+534T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | chrX | 71130748 | |||||||
| chrX:71131125 | C | CT | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(39): Show |
86 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.4048-405dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | ||||||
| chrX:71131125 | C | CTT | 5 | a0001c0001t0001g0035 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
7 | HG01106.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.4048-406_4048-405d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | ||||||
| chrX:71131125 | C | CTTTT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0121 others(8): Show |
17 | HG00423.hp2 HG01081.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.4048-408_4048-405d others(6): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | ||||||
| chrX:71131125 | CT | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(22): Show |
46 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.4048-405delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 28/44 | INFO_REALIGN_3_PRIME | chrX | 71131125 | ||||||
| chrX:71131669 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18949.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.4119+48A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131669 | |||||||
| chrX:71131796 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4119+175G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131796 | |||||||
| chrX:71131917 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4120-156C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131917 | |||||||
| chrX:71131988 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
141 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.4120-85C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 29/44 | chrX | 71131988 | |||||||
| chrX:71132233 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4253+27T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 30/44 | chrX | 71132233 | |||||||
| chrX:71132293 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4254-84A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 30/44 | chrX | 71132293 | |||||||
| chrX:71132327 | C | T | 1 | a0001c0003t0001g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4254-50C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 30/44 | chrX | 71132327 | |||||||
| chrX:71132567 | T | C | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.4415+29T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132567 | |||||||
| chrX:71132666 | A | G | 8 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(5): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.4415+128A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132666 | |||||||
| chrX:71132762 | T | C | 1 | a0006c0015t0001g0055 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-83T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132762 | |||||||
| chrX:71132767 | C | CCTCTT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0020 others(20): Show |
42 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.4416-20_4416-16dup others(5): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | C | CCTCTTCT others(3): Show |
10 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0057 others(7): Show |
15 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.4416-25_4416-16dup others(10): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | C | CCTCTTCT others(8): Show |
6 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0082 others(3): Show |
7 | HG00423.hp1 HG01109.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4416-30_4416-16dup others(15): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | C | CCTCTTCT others(13): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0122 |
3 | HG00423.hp2 HG00741.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4416-35_4416-16dup others(20): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | C | CCTCTTCT others(18): Show |
1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4416-40_4416-16dup others(25): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | C | T | 1 | a0006c0015t0001g0055 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-78C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132767 | |||||||
| chrX:71132767 | CCTCTT | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(19): Show |
52 | HG00639.hp1 HG00673.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.4416-20_4416-16del others(5): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | CCTCTTCT others(3): Show |
C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0024 others(6): Show |
15 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.4416-25_4416-16del others(10): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | CCTCTTCT others(8): Show |
C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0088 others(4): Show |
9 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.4416-30_4416-16del others(15): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | CCTCTTCT others(13): Show |
C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0050 others(2): Show |
7 | HG02280.hp1 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.4416-35_4416-16del others(20): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | CCTCTTCT others(18): Show |
C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0071 others(13): Show |
32 | HG00741.hp2 HG01884.hp2 HG02165.hp2 others(29): Show |
intron_variant | MODIFIER | c.4416-40_4416-16del others(25): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | CCTCTTCT others(23): Show |
C | 7 | a0001c0002t0001g0007 a0001c0002t0001g0011 a0001c0002t0001g0134 others(4): Show |
18 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.4416-45_4416-16del others(30): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132767 | CCTCTTCT others(28): Show |
C | 1 | a0001c0002t0001g0136 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4416-50_4416-16del others(35): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | 71132767 | ||||||
| chrX:71132788 | C | CCTTCTCT others(3): Show |
1 | a0006c0015t0001g0055 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4416-57_4416-56ins others(10): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132788 | |||||||
| chrX:71132795 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4416-50C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | chrX | 71132795 | |||||||
| chrX:71132991 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4527+35G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 32/44 | chrX | 71132991 | |||||||
| chrX:71133102 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4528-21T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 32/44 | chrX | 71133102 | |||||||
| chrX:71133237 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4617+25A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133237 | |||||||
| chrX:71133263 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0089 |
3 | HG02647.hp1 HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4617+51G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133263 | |||||||
| chrX:71133336 | G | GT | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(10): Show |
18 | HG00733.hp1 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.4617+138dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71133336 | ||||||
| chrX:71133545 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4617+333G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133545 | |||||||
| chrX:71133605 | A | T | 2 | a0001c0003t0001g0065 a0001c0003t0001g0079 |
2 | NA18944.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.4617+393A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133605 | |||||||
| chrX:71133609 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4617+397C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133609 | |||||||
| chrX:71133814 | G | A | 4 | a0001c0004t0001g0012 a0001c0004t0001g0021 a0001c0004t0001g0041 others(1): Show |
8 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.4618-543G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71133814 | |||||||
| chrX:71134046 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.4618-311G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71134046 | |||||||
| chrX:71134217 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4618-140C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71134217 | |||||||
| chrX:71134230 | C | CA | 25 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0032 others(22): Show |
40 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.4618-106dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71134230 | ||||||
| chrX:71134230 | CA | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0052 others(8): Show |
14 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.4618-106delA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | INFO_REALIGN_3_PRIME | chrX | 71134230 | ||||||
| chrX:71134252 | C | A | 2 | a0001c0002t0001g0011 a0004c0019t0001g0011 |
5 | HG00099.hp1 HG00642.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.4618-105C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 33/44 | chrX | 71134252 | |||||||
| chrX:71134585 | T | C | 1 | a0008c0010t0001g0077 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4727+119T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | chrX | 71134585 | |||||||
| chrX:71134586 | C | T | 1 | a0008c0010t0001g0077 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4727+120C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | chrX | 71134586 | |||||||
| chrX:71134676 | TTTC | T | 3 | a0001c0001t0001g0076 a0001c0013t0001g0131 a0001c0018t0001g0130 |
3 | HG02615.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4728-31_4728-29del others(3): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 34/44 | INFO_REALIGN_3_PRIME | chrX | 71134676 | ||||||
| chrX:71134961 | T | G | 1 | a0001c0001t0001g0029 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4863+113T>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/44 | chrX | 71134961 | |||||||
| chrX:71135038 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0138 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4864-54C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 35/44 | chrX | 71135038 | |||||||
| chrX:71135325 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5025+72T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135325 | |||||||
| chrX:71135373 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.5025+120C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135373 | |||||||
| chrX:71135408 | CTT | C | 11 | a0001c0001t0001g0076 a0001c0002t0001g0007 a0001c0002t0001g0011 others(8): Show |
22 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.5025+156_5025+157d others(4): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135408 | |||||||
| chrX:71135494 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0082 a0001c0001t0001g0083 |
4 | NA18979.hp2 NA19070.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.5025+241T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135494 | |||||||
| chrX:71135522 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5025+269C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135522 | |||||||
| chrX:71135538 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5025+285A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135538 | |||||||
| chrX:71135861 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.5026-420C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71135861 | |||||||
| chrX:71136012 | C | G | 1 | a0008c0010t0001g0077 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5026-269C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136012 | |||||||
| chrX:71136029 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5026-252G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136029 | |||||||
| chrX:71136032 | A | T | 11 | a0001c0001t0001g0076 a0001c0002t0001g0007 a0001c0002t0001g0011 others(8): Show |
22 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.5026-249A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136032 | |||||||
| chrX:71136091 | TGCCCCAC others(34): Show |
T | 1 | a0007c0016t0001g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5026-189_5026-149d others(43): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136091 | |||||||
| chrX:71136092 | G | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
162 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(159): Show |
intron_variant | MODIFIER | c.5026-189G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 36/44 | chrX | 71136092 | |||||||
| chrX:71136662 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | splice_region_variant&intron_variant | LOW | c.5400+7G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136662 | |||||||
| chrX:71136792 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
172 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(169): Show |
intron_variant | MODIFIER | c.5401-87T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136792 | |||||||
| chrX:71136833 | C | A | 1 | a0008c0010t0001g0077 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.5401-46C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136833 | |||||||
| chrX:71136854 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
45 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.5401-25C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 37/44 | chrX | 71136854 | |||||||
| chrX:71137475 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5749-83A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 39/44 | chrX | 71137475 | |||||||
| chrX:71138080 | C | T | 1 | a0001c0006t0001g0058 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6044+137C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138080 | |||||||
| chrX:71138382 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0034 others(8): Show |
18 | HG00423.hp2 HG00735.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.6044+439C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138382 | |||||||
| chrX:71138580 | T | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
45 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.6044+637T>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138580 | |||||||
| chrX:71138593 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6044+650A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138593 | |||||||
| chrX:71138596 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6044+653C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138596 | |||||||
| chrX:71138660 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6044+717A>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138660 | |||||||
| chrX:71138886 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6044+943A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71138886 | |||||||
| chrX:71139656 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG00423.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.6045-979T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71139656 | |||||||
| chrX:71139821 | C | A | 1 | a0007c0016t0001g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6045-814C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71139821 | |||||||
| chrX:71140080 | C | CT | 13 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0063 others(10): Show |
24 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.6045-538dupT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140080 | ||||||
| chrX:71140080 | CT | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0048 others(4): Show |
11 | HG01891.hp1 HG02559.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.6045-538delT | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | INFO_REALIGN_3_PRIME | chrX | 71140080 | ||||||
| chrX:71140144 | A | G | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0086 others(3): Show |
8 | HG01123.hp2 HG01361.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.6045-491A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140144 | |||||||
| chrX:71140246 | T | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0110 others(5): Show |
11 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.6045-389T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140246 | |||||||
| chrX:71140274 | G | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0138 a0001c0001t0001g0139 |
4 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.6045-361G>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140274 | |||||||
| chrX:71140366 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.6045-269G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 41/44 | chrX | 71140366 | |||||||
| chrX:71140894 | C | A | 1 | a0007c0016t0001g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6267+37C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71140894 | |||||||
| chrX:71141114 | A | G | 1 | a0007c0016t0001g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-116A>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71141114 | |||||||
| chrX:71141116 | G | C | 1 | a0007c0016t0001g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-114G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71141116 | |||||||
| chrX:71141117 | C | A | 1 | a0007c0016t0001g0113 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.6268-113C>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 42/44 | chrX | 71141117 | |||||||
| chrX:71141423 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
45 | HG00741.hp2 HG01123.hp2 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.6408+53C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141423 | |||||||
| chrX:71141618 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6408+248G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141618 | |||||||
| chrX:71141758 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
163 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(160): Show |
intron_variant | MODIFIER | c.6409-125T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141758 | |||||||
| chrX:71141769 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(41): Show |
84 | HG00423.hp2 HG00639.hp2 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.6409-114T>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | chrX | 71141769 | |||||||
| chrX:71141801 | C | CA | 20 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0062 others(17): Show |
35 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.6409-71dupA | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 43/44 | INFO_REALIGN_3_PRIME | chrX | 71141801 | ||||||
| chrX:71142015 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6490+51G>C | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142015 | |||||||
| chrX:71142016 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.6490+52C>G | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142016 | |||||||
| chrX:71142087 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.6491-88C>T | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142087 | |||||||
| chrX:71142117 | G | A | 13 | a0001c0001t0001g0035 a0001c0001t0001g0139 a0001c0002t0001g0007 others(10): Show |
29 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.6491-58G>A | MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 44/44 | chrX | 71142117 |