Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9441 |
| ensemblid | ENSG00000105085.11 |
| hgncid | 2376 |
| symbol | MED26 |
| name | mediator complex subunit 26 |
| refseq_nuc | NM_004831.5 |
| refseq_prot | NP_004822.2 |
| ensembl_nuc | ENST00000263390.8 |
| ensembl_prot | ENSP00000263390.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 16574919 |
| end | 16628204 |
| strand | - |
| ver | v1.2 |
| region | chr19:16574919-16628204 |
| region5000 | chr19:16569919-16633204 |
| regionname0 | MED26_chr19_16574919_16628204 |
| regionname5000 | MED26_chr19_16569919_16633204 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 600 | 265 | 77 | 62 | 78 | 6 | 40 | 46 | MED26_chr19_16569919_16633204 | MED26 | MTAAP others(595): Show |
chr19 | 16569919 | 16633204 |
| a0002 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | MTAAP others(595): Show |
chr19 | 16569919 | 16633204 |
| a0003 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | MTAAP others(595): Show |
chr19 | 16569919 | 16633204 |
| a0004 | 0/0 | 600 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | MTAAP others(595): Show |
chr19 | 16569919 | 16633204 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1800 | 248 | 64 | 60 | 77 | 6 | 39 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0001c0002 | 0/0 | 1800 | 12 | 11 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0001c0003 | 0/0 | 1800 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0001c0005 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0001c0006 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0001c0009 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0002c0007 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0003c0008 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 | ||
| a0004c0004 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ATGAC others(1795): Show |
chr19 | 16569919 | 16633204 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3172 | 231 | 54 | 56 | 76 | 6 | 37 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0001t0002 | 0/0 | 3171 | 11 | 7 | 3 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3166): Show |
chr19 | 16569919 | 16633204 |
| a0001c0001t0004 | 0/0 | 3172 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0001t0005 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3166): Show |
chr19 | 16569919 | 16633204 |
| a0001c0001t0006 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0001t0007 | 0/0 | 3172 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0001t0008 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0001t0009 | 0/0 | 3172 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0002t0001 | 0/0 | 3172 | 12 | 11 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0003t0001 | 0/0 | 3172 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0005t0003 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3166): Show |
chr19 | 16569919 | 16633204 |
| a0001c0006t0001 | 0/0 | 3172 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0001c0009t0001 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0002c0007t0001 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0003c0008t0001 | 0/0 | 3172 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3167): Show |
chr19 | 16569919 | 16633204 |
| a0004c0004t0002 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | ACTGG others(3166): Show |
chr19 | 16569919 | 16633204 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 3 | 6 | 0 | 4 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0002 | 1/0 | 8 | 0 | 1 | 6 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0004 | 0/0 | 6 | 3 | 1 | 0 | 1 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0003t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0005t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0001c0009t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0002c0007t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0003c0008t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| a0004c0004t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | GBR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0164 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0138 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02280 | hp1 | a0001 | c0005 | t0003 | g0077 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0171 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02922 | hp2 | a0002 | c0007 | t0001 | g0034 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02965 | hp1 | a0001 | c0009 | t0001 | g0132 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02976 | hp1 | a0003 | c0008 | t0001 | g0092 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03516 | hp2 | a0004 | c0004 | t0002 | g0196 | AFR | ESN | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0026 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18949 | hp1 | a0001 | c0006 | t0001 | g0082 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | YRI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ASW | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ASW | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | USA | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | LWK | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0187 | REF | REF | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | MED26_chr19_16569919_16633204 | MED26 | chr19 | 16569919 | 16633204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16576265 | C | T | 1 | a0002 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1565G>A | p.Arg522Gln | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1826/3172 | 1565/1803 | 522/600 | chr19 | 16576265 | |||
| chr19:16576775 | G | A | 1 | a0003 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1055C>T | p.Ala352Val | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1316/3172 | 1055/1803 | 352/600 | chr19 | 16576775 | |||
| chr19:16578405 | C | T | 1 | a0004 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.77G>A | p.Arg26Gln | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/3 | 338/3172 | 77/1803 | 26/600 | chr19 | 16578405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16576591 | C | T | 1 | a0001c0006 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.1239G>A | p.Ala413Ala | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1500/3172 | 1239/1803 | 413/600 | chr19 | 16576591 | |||
| chr19:16576891 | C | T | 1 | a0001c0005 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.939G>A | p.Pro313Pro | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1200/3172 | 939/1803 | 313/600 | chr19 | 16576891 | |||
| chr19:16576942 | G | A | 1 | a0001c0009 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.888C>T | p.Ser296Ser | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1149/3172 | 888/1803 | 296/600 | chr19 | 16576942 | |||
| chr19:16577059 | G | A | 1 | a0001c0002 | 12 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
synonymous_variant | LOW | c.771C>T | p.Asp257Asp | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1032/3172 | 771/1803 | 257/600 | chr19 | 16577059 | |||
| chr19:16577647 | G | A | 1 | a0001c0003 | 2 | HG00738.hp1 HG03927.hp2 |
synonymous_variant | LOW | c.183C>T | p.Arg61Arg | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 444/3172 | 183/1803 | 61/600 | chr19 | 16577647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16574921 | GT | G | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0005t0003 others(1): Show |
14 | HG01070.hp2 HG01071.hp2 HG01943.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1105delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 1105 | chr19 | 16574921 | ||||||
| chr19:16575124 | C | T | 1 | a0001c0001t0007 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 903 | chr19 | 16575124 | ||||||
| chr19:16575128 | G | A | 1 | a0001c0001t0008 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 899 | chr19 | 16575128 | ||||||
| chr19:16575521 | G | T | 1 | a0001c0001t0006 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 506 | chr19 | 16575521 | ||||||
| chr19:16575634 | A | G | 1 | a0001c0001t0005 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 393 | chr19 | 16575634 | ||||||
| chr19:16575809 | G | A | 1 | a0001c0001t0009 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 218 | chr19 | 16575809 | ||||||
| chr19:16575894 | C | T | 1 | a0001c0001t0004 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 133 | chr19 | 16575894 | ||||||
| chr19:16576025 | G | T | 1 | a0001c0005t0003 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 3/3 | 2 | chr19 | 16576025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16577714 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.148-32G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16577714 | |||||||
| chr19:16577943 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.148-261G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16577943 | |||||||
| chr19:16578017 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147+318C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578017 | |||||||
| chr19:16578069 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147+266A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578069 | |||||||
| chr19:16578270 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.147+65G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578270 | |||||||
| chr19:16578291 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+44G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 2/2 | chr19 | 16578291 | |||||||
| chr19:16578429 | T | A | 1 | a0001c0001t0001g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.73-20A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578429 | |||||||
| chr19:16578603 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0072 |
2 | NA18991.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.73-194G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578603 | |||||||
| chr19:16578804 | T | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-395A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578804 | |||||||
| chr19:16578828 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-419G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578828 | |||||||
| chr19:16578890 | C | T | 1 | a0001c0001t0005g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-481G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578890 | |||||||
| chr19:16578895 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-486C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578895 | |||||||
| chr19:16578929 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | NA18612.hp2 NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.73-520G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16578929 | |||||||
| chr19:16579106 | T | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0060 |
7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-697A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579106 | |||||||
| chr19:16579162 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.73-753C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579162 | |||||||
| chr19:16579424 | G | A | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-1015C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579424 | |||||||
| chr19:16579705 | C | G | 1 | a0001c0001t0007g0138 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.73-1296G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579705 | |||||||
| chr19:16579964 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.73-1555T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579964 | |||||||
| chr19:16579991 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.73-1582G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16579991 | |||||||
| chr19:16580002 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-1593G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580002 | |||||||
| chr19:16580202 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0169 |
2 | HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.73-1793C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580202 | |||||||
| chr19:16580215 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG02451.hp1 HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.73-1806C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580215 | |||||||
| chr19:16580493 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-2084G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580493 | |||||||
| chr19:16580541 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0058 others(1): Show |
7 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-2132C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580541 | |||||||
| chr19:16580729 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.73-2320C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580729 | |||||||
| chr19:16580818 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.73-2409G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580818 | |||||||
| chr19:16580847 | T | G | 1 | a0001c0009t0001g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.73-2438A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16580847 | |||||||
| chr19:16581170 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.73-2761C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581170 | |||||||
| chr19:16581283 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.73-2874T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581283 | |||||||
| chr19:16581441 | C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-3032G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581441 | |||||||
| chr19:16581518 | A | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-3109T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581518 | |||||||
| chr19:16581817 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-3408G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581817 | |||||||
| chr19:16581895 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-3486G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581895 | |||||||
| chr19:16581896 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.73-3487C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581896 | |||||||
| chr19:16581911 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-3502G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581911 | |||||||
| chr19:16581916 | G | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-3507C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16581916 | |||||||
| chr19:16582090 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.73-3681G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582090 | |||||||
| chr19:16582126 | A | G | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-3717T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582126 | |||||||
| chr19:16582143 | G | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0060 others(4): Show |
14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-3734C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582143 | |||||||
| chr19:16582182 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.73-3773C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582182 | |||||||
| chr19:16582213 | G | T | 1 | a0001c0003t0001g0026 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.73-3804C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582213 | |||||||
| chr19:16582297 | A | AT | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(26): Show |
36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.73-3889dupA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582297 | |||||||
| chr19:16582383 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.73-3974C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582383 | |||||||
| chr19:16582447 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0174 |
2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.73-4038G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582447 | |||||||
| chr19:16582461 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | NA18612.hp2 NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.73-4052A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582461 | |||||||
| chr19:16582578 | G | C | 1 | a0001c0001t0002g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.73-4169C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582578 | |||||||
| chr19:16582633 | G | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-4224C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582633 | |||||||
| chr19:16582639 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.73-4230G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582639 | |||||||
| chr19:16582701 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-4292C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582701 | |||||||
| chr19:16582794 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(26): Show |
36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.73-4385A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16582794 | |||||||
| chr19:16583006 | T | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-4597A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583006 | |||||||
| chr19:16583079 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0199 |
3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-4670C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583079 | |||||||
| chr19:16583095 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-4686G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583095 | |||||||
| chr19:16583283 | T | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-4874A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583283 | |||||||
| chr19:16583389 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.73-4980G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583389 | |||||||
| chr19:16583475 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(30): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-5066C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583475 | |||||||
| chr19:16583584 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-5175G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583584 | |||||||
| chr19:16583678 | G | GCAGGTCC others(4): Show |
1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-5280_73-5270dup others(11): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583678 | |||||||
| chr19:16583701 | T | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-5292A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583701 | |||||||
| chr19:16583737 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-5328G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583737 | |||||||
| chr19:16583799 | T | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(70): Show |
95 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.73-5390A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583799 | |||||||
| chr19:16583888 | C | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-5479G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16583888 | |||||||
| chr19:16584097 | A | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-5688T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584097 | |||||||
| chr19:16584168 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0053 |
2 | HG01891.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.73-5759C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584168 | |||||||
| chr19:16584287 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-5878T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584287 | |||||||
| chr19:16584300 | C | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0125 |
3 | NA19002.hp1 NA19074.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.73-5891G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584300 | |||||||
| chr19:16584300 | C | T | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-5891G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584300 | |||||||
| chr19:16584301 | C | A | 10 | a0001c0001t0001g0102 a0001c0002t0001g0017 a0001c0002t0001g0018 others(7): Show |
13 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-5892G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584301 | |||||||
| chr19:16584302 | C | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-5893G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584302 | |||||||
| chr19:16584303 | CG | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0064 others(13): Show |
23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-5895delC | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584303 | |||||||
| chr19:16584304 | G | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0006g0078 others(1): Show |
4 | HG00673.hp1 HG02280.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-5895C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584304 | |||||||
| chr19:16584306 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.73-5897G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584306 | |||||||
| chr19:16584311 | C | CA | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
47 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.73-5903dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584311 | |||||||
| chr19:16584426 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-6017C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584426 | |||||||
| chr19:16584445 | T | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-6036A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584445 | |||||||
| chr19:16584470 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.73-6061C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16584470 | |||||||
| chr19:16585070 | T | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.73-6661A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585070 | |||||||
| chr19:16585256 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.73-6847C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585256 | |||||||
| chr19:16585288 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(10): Show |
20 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.73-6879C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585288 | |||||||
| chr19:16585439 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-7030C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585439 | |||||||
| chr19:16585710 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-7301C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585710 | |||||||
| chr19:16585735 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(13): Show |
23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-7326G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585735 | |||||||
| chr19:16585763 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 |
4 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-7354A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585763 | |||||||
| chr19:16585858 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.73-7449T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585858 | |||||||
| chr19:16585907 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.73-7498G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585907 | |||||||
| chr19:16585909 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.73-7500G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16585909 | |||||||
| chr19:16586015 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.73-7606G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586015 | |||||||
| chr19:16586265 | A | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-7856T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586265 | |||||||
| chr19:16586279 | G | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-7870C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586279 | |||||||
| chr19:16586432 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.73-8023G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586432 | |||||||
| chr19:16586481 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0088 |
2 | HG00673.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.73-8072G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586481 | |||||||
| chr19:16586539 | C | T | 1 | a0001c0001t0004g0185 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.73-8130G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586539 | |||||||
| chr19:16586653 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.73-8244G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586653 | |||||||
| chr19:16586688 | G | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(30): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-8279C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586688 | |||||||
| chr19:16586897 | T | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.73-8488A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586897 | |||||||
| chr19:16586913 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.73-8504A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16586913 | |||||||
| chr19:16587023 | A | C | 1 | a0001c0001t0001g0025 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.73-8614T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587023 | |||||||
| chr19:16587093 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.73-8684C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587093 | |||||||
| chr19:16587095 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0013 others(17): Show |
26 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.73-8686C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587095 | |||||||
| chr19:16587119 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0042 |
4 | HG01256.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-8710G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587119 | |||||||
| chr19:16587764 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-9355A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587764 | |||||||
| chr19:16587805 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-9396T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587805 | |||||||
| chr19:16587914 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.73-9505G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16587914 | |||||||
| chr19:16588120 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-9711G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588120 | |||||||
| chr19:16588159 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.73-9750C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588159 | |||||||
| chr19:16588320 | T | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-9911A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588320 | |||||||
| chr19:16588513 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.73-10104C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588513 | |||||||
| chr19:16588529 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(30): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-10120C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588529 | |||||||
| chr19:16588532 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.73-10123G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588532 | |||||||
| chr19:16588804 | C | T | 1 | a0001c0003t0001g0026 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.73-10395G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588804 | |||||||
| chr19:16588809 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-10400G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588809 | |||||||
| chr19:16588875 | G | A | 18 | a0001c0001t0002g0028 a0001c0001t0002g0097 a0001c0001t0002g0098 others(15): Show |
22 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-10466C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16588875 | |||||||
| chr19:16589002 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(50): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.73-10593G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589002 | |||||||
| chr19:16589041 | C | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0032 others(18): Show |
24 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.73-10632G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589041 | |||||||
| chr19:16589081 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-10672C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589081 | |||||||
| chr19:16589209 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-10800C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589209 | |||||||
| chr19:16589216 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.73-10807C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589216 | |||||||
| chr19:16589240 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
157 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.73-10831T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589240 | |||||||
| chr19:16589441 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.73-11032C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589441 | |||||||
| chr19:16589933 | C | T | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.73-11524G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16589933 | |||||||
| chr19:16590076 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-11667G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590076 | |||||||
| chr19:16590331 | C | A | 5 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0194 others(2): Show |
5 | HG02280.hp2 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-11922G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590331 | |||||||
| chr19:16590429 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(30): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.73-12020G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590429 | |||||||
| chr19:16590645 | G | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 others(1): Show |
4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-12236C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590645 | |||||||
| chr19:16590768 | C | T | 8 | a0001c0001t0002g0028 a0001c0001t0002g0097 a0001c0001t0002g0098 others(5): Show |
9 | HG01070.hp2 HG01071.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.73-12359G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590768 | |||||||
| chr19:16590776 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-12367T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590776 | |||||||
| chr19:16590822 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73-12413C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590822 | |||||||
| chr19:16590899 | G | GCACC | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-12491_73-12490i others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590899 | |||||||
| chr19:16590925 | A | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-12516T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16590925 | |||||||
| chr19:16591043 | AAAATAAA others(14): Show |
A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-12655_73-12635d others(23): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591043 | |||||||
| chr19:16591048 | A | AAAAT | 4 | a0001c0001t0001g0009 a0001c0001t0001g0152 a0001c0002t0001g0017 others(1): Show |
4 | HG02015.hp1 HG02109.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-12643_73-12640d others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | |||||||
| chr19:16591048 | AAAAT | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
86 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.73-12643_73-12640d others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | |||||||
| chr19:16591048 | AAAATAAA others(1): Show |
A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
59 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.73-12647_73-12640d others(10): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | |||||||
| chr19:16591048 | AAAATAAA others(5): Show |
A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0016 others(16): Show |
26 | HG01070.hp1 HG01192.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.73-12651_73-12640d others(14): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | |||||||
| chr19:16591048 | AAAATAAA others(9): Show |
A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0022 others(6): Show |
10 | HG00609.hp1 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-12655_73-12640d others(18): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | |||||||
| chr19:16591048 | AAAATAAA others(13): Show |
A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-12659_73-12640d others(22): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591048 | |||||||
| chr19:16591053 | AAATAAAT others(4): Show |
A | 1 | a0001c0001t0001g0010 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.73-12655_73-12645d others(13): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591053 | |||||||
| chr19:16591142 | A | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-12733T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591142 | |||||||
| chr19:16591295 | C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-12886G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591295 | |||||||
| chr19:16591321 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.73-12912C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591321 | |||||||
| chr19:16591352 | ATG | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-12945_73-12944d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591352 | |||||||
| chr19:16591459 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.73-13050A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591459 | |||||||
| chr19:16591659 | C | T | 1 | a0001c0001t0002g0028 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.73-13250G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591659 | |||||||
| chr19:16591992 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.73-13583G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16591992 | |||||||
| chr19:16592209 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.73-13800A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592209 | |||||||
| chr19:16592541 | C | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(24): Show |
34 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-14132G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592541 | |||||||
| chr19:16592541 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-14132G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592541 | |||||||
| chr19:16592542 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-14133C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592542 | |||||||
| chr19:16592626 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-14217C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592626 | |||||||
| chr19:16592877 | C | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0060 others(4): Show |
14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-14468G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592877 | |||||||
| chr19:16592999 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(13): Show |
23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-14590G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16592999 | |||||||
| chr19:16593025 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.73-14616C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593025 | |||||||
| chr19:16593099 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-14690T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593099 | |||||||
| chr19:16593409 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-15000T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593409 | |||||||
| chr19:16593520 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-15111C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593520 | |||||||
| chr19:16593770 | A | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-15361T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593770 | |||||||
| chr19:16593928 | C | T | 1 | a0001c0001t0008g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.73-15519G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593928 | |||||||
| chr19:16593970 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.73-15561T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16593970 | |||||||
| chr19:16594031 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.73-15622C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16594031 | |||||||
| chr19:16594532 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.73-16123A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16594532 | |||||||
| chr19:16594896 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-16487C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16594896 | |||||||
| chr19:16595201 | G | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-16792C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595201 | |||||||
| chr19:16595327 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0199 |
3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-16918C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595327 | |||||||
| chr19:16595386 | T | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-16977A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595386 | |||||||
| chr19:16595437 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0060 others(4): Show |
14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-17028G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595437 | |||||||
| chr19:16595485 | T | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-17076A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595485 | |||||||
| chr19:16595621 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.73-17212T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16595621 | |||||||
| chr19:16596248 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.73-17839A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596248 | |||||||
| chr19:16596294 | C | G | 1 | a0001c0001t0009g0171 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.73-17885G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596294 | |||||||
| chr19:16596857 | G | GC | 2 | a0001c0001t0002g0028 a0001c0001t0002g0199 |
3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-18449dupG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596857 | |||||||
| chr19:16596873 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(13): Show |
23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-18464G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596873 | |||||||
| chr19:16596991 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.73-18582T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16596991 | |||||||
| chr19:16597087 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.73-18678G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597087 | |||||||
| chr19:16597205 | T | TA | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(13): Show |
23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-18797dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597205 | |||||||
| chr19:16597259 | A | G | 1 | a0001c0001t0008g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.73-18850T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597259 | |||||||
| chr19:16597369 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.73-18960G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597369 | |||||||
| chr19:16597622 | G | A | 1 | a0002c0007t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-19213C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597622 | |||||||
| chr19:16597623 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.73-19214G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597623 | |||||||
| chr19:16597774 | G | A | 1 | a0001c0002t0001g0017 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.73-19365C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597774 | |||||||
| chr19:16597810 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(13): Show |
23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.73-19401G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597810 | |||||||
| chr19:16597923 | T | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.73-19514A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16597923 | |||||||
| chr19:16598117 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(24): Show |
34 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-19708G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598117 | |||||||
| chr19:16598193 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0199 |
3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-19784G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598193 | |||||||
| chr19:16598200 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.73-19791C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598200 | |||||||
| chr19:16598229 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.73-19820G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598229 | |||||||
| chr19:16598336 | C | CA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.73-19928dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598336 | |||||||
| chr19:16598336 | C | CAA | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(38): Show |
51 | HG00621.hp1 HG00741.hp1 HG01256.hp1 others(48): Show |
intron_variant | MODIFIER | c.73-19929_73-19928d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598336 | |||||||
| chr19:16598336 | C | CAAA | 7 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0046 others(4): Show |
7 | HG01167.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-19930_73-19928d others(5): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598336 | |||||||
| chr19:16598481 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0139 a0001c0001t0001g0141 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-20072A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598481 | |||||||
| chr19:16598680 | C | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0060 |
7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-20271G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598680 | |||||||
| chr19:16598804 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.73-20395C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598804 | |||||||
| chr19:16598852 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.73-20443A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598852 | |||||||
| chr19:16598919 | T | TA | 25 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0016 others(22): Show |
35 | HG00609.hp2 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.73-20511dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598919 | |||||||
| chr19:16598935 | C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.73-20526G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16598935 | |||||||
| chr19:16599114 | G | C | 1 | a0001c0002t0001g0017 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.73-20705C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599114 | |||||||
| chr19:16599197 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0129 a0001c0001t0001g0186 |
4 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-20788G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599197 | |||||||
| chr19:16599211 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.73-20802G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599211 | |||||||
| chr19:16599759 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.73-21350C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599759 | |||||||
| chr19:16599872 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-21463T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599872 | |||||||
| chr19:16599951 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.73-21542T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16599951 | |||||||
| chr19:16600183 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0139 a0001c0001t0001g0141 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-21774T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600183 | |||||||
| chr19:16600266 | T | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-21857A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600266 | |||||||
| chr19:16600454 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.73-22045G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600454 | |||||||
| chr19:16600461 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.73-22052T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600461 | |||||||
| chr19:16600984 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.73-22575G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16600984 | |||||||
| chr19:16601136 | G | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-22727C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601136 | |||||||
| chr19:16601159 | C | CT | 48 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(45): Show |
63 | HG00621.hp1 HG01192.hp2 HG01256.hp1 others(60): Show |
intron_variant | MODIFIER | c.73-22751dupA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601159 | |||||||
| chr19:16601299 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-22890C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601299 | |||||||
| chr19:16601419 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-23010A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601419 | |||||||
| chr19:16601516 | C | T | 1 | a0003c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73-23107G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601516 | |||||||
| chr19:16601523 | G | A | 1 | a0001c0009t0001g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.73-23114C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601523 | |||||||
| chr19:16601652 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA19002.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.73-23243G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601652 | |||||||
| chr19:16601657 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-23248T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601657 | |||||||
| chr19:16601780 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 |
4 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-23371G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601780 | |||||||
| chr19:16601800 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.73-23391G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601800 | |||||||
| chr19:16601889 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0139 others(5): Show |
11 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-23480G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16601889 | |||||||
| chr19:16602091 | G | A | 1 | a0001c0001t0005g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-23682C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602091 | |||||||
| chr19:16602137 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.73-23728T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602137 | |||||||
| chr19:16602210 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.73-23801T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602210 | |||||||
| chr19:16602270 | G | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 others(1): Show |
4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-23861C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602270 | |||||||
| chr19:16602307 | C | G | 1 | a0001c0001t0001g0015 | 2 | HG01884.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.73-23898G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602307 | |||||||
| chr19:16602459 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.73-24050C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602459 | |||||||
| chr19:16602521 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(24): Show |
34 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.73-24112G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602521 | |||||||
| chr19:16602744 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-24335G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602744 | |||||||
| chr19:16602969 | A | C | 1 | a0003c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.73-24560T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16602969 | |||||||
| chr19:16603034 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.73-24625G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603034 | |||||||
| chr19:16603085 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.73-24676G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603085 | |||||||
| chr19:16603159 | A | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.72+24713T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603159 | |||||||
| chr19:16603470 | A | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+24402T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603470 | |||||||
| chr19:16603471 | A | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+24401T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603471 | |||||||
| chr19:16603657 | T | C | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72+24215A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603657 | |||||||
| chr19:16603791 | T | TCTGGCTC others(7): Show |
1 | a0001c0001t0002g0197 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.72+24067_72+24080d others(16): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16603791 | |||||||
| chr19:16604011 | T | A | 2 | a0001c0001t0001g0102 a0003c0008t0001g0092 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.72+23861A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604011 | |||||||
| chr19:16604155 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(25): Show |
35 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.72+23717A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604155 | |||||||
| chr19:16604323 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.72+23549A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604323 | |||||||
| chr19:16604420 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 |
4 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+23452G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604420 | |||||||
| chr19:16604461 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.72+23411C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604461 | |||||||
| chr19:16604486 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.72+23386G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604486 | |||||||
| chr19:16604647 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.72+23225A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604647 | |||||||
| chr19:16604795 | C | A | 7 | a0001c0001t0002g0028 a0001c0001t0002g0194 a0001c0001t0002g0195 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+23077G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604795 | |||||||
| chr19:16604812 | C | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.72+23060G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604812 | |||||||
| chr19:16604823 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+23049G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604823 | |||||||
| chr19:16604887 | A | T | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+22985T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16604887 | |||||||
| chr19:16605047 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.72+22825C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605047 | |||||||
| chr19:16605080 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.72+22792T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605080 | |||||||
| chr19:16605148 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.72+22724G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605148 | |||||||
| chr19:16605199 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0179 |
2 | HG03490.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.72+22673A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605199 | |||||||
| chr19:16605229 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+22643G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605229 | |||||||
| chr19:16605254 | T | C | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+22618A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605254 | |||||||
| chr19:16605314 | G | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(10): Show |
20 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.72+22558C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605314 | |||||||
| chr19:16605536 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+22336C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605536 | |||||||
| chr19:16605629 | T | G | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.72+22243A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605629 | |||||||
| chr19:16605769 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+22103C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16605769 | |||||||
| chr19:16606030 | G | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01934.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.72+21842C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606030 | |||||||
| chr19:16606034 | G | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+21838C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606034 | |||||||
| chr19:16606092 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0060 |
7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+21780G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606092 | |||||||
| chr19:16606421 | G | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0060 |
7 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+21451C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606421 | |||||||
| chr19:16606661 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.72+21211A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606661 | |||||||
| chr19:16606732 | A | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+21140T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606732 | |||||||
| chr19:16606824 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.72+21048A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606824 | |||||||
| chr19:16606864 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+21008T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606864 | |||||||
| chr19:16606875 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.72+20997C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606875 | |||||||
| chr19:16606882 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00544.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.72+20990G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606882 | |||||||
| chr19:16606943 | A | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
7 | HG00639.hp2 HG01168.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+20929T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16606943 | |||||||
| chr19:16607128 | T | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0060 others(4): Show |
14 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.72+20744A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607128 | |||||||
| chr19:16607191 | T | TA | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(26): Show |
36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.72+20680dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607191 | |||||||
| chr19:16607261 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.72+20611G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607261 | |||||||
| chr19:16607375 | G | GA | 11 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
12 | HG00733.hp1 HG00735.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+20496dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607375 | |||||||
| chr19:16607375 | GA | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0060 a0001c0001t0001g0102 others(3): Show |
11 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+20496delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607375 | |||||||
| chr19:16607376 | A | G | 7 | a0001c0001t0001g0125 a0001c0001t0001g0161 a0001c0001t0002g0097 others(4): Show |
7 | HG00741.hp2 HG02280.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+20496T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607376 | |||||||
| chr19:16607402 | T | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+20470A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607402 | |||||||
| chr19:16607448 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.72+20424G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607448 | |||||||
| chr19:16607698 | C | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+20174G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607698 | |||||||
| chr19:16607730 | A | AT | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+20141dupA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607730 | |||||||
| chr19:16607751 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+20121G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607751 | |||||||
| chr19:16607798 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.72+20074G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607798 | |||||||
| chr19:16607806 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.72+20066C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607806 | |||||||
| chr19:16607871 | C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+20001G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607871 | |||||||
| chr19:16607902 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0129 a0001c0001t0001g0186 |
4 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+19970T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16607902 | |||||||
| chr19:16608185 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.72+19687G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608185 | |||||||
| chr19:16608251 | T | C | 7 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0152 others(4): Show |
10 | HG00609.hp2 HG00621.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+19621A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608251 | |||||||
| chr19:16608644 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+19228A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608644 | |||||||
| chr19:16608705 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.72+19167C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608705 | |||||||
| chr19:16608958 | T | C | 1 | a0001c0002t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.72+18914A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16608958 | |||||||
| chr19:16609023 | G | A | 1 | a0001c0009t0001g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72+18849C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609023 | |||||||
| chr19:16609193 | T | C | 1 | a0001c0003t0001g0026 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.72+18679A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609193 | |||||||
| chr19:16609198 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+18674C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609198 | |||||||
| chr19:16609215 | A | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(28): Show |
40 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.72+18657T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609215 | |||||||
| chr19:16609236 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+18636G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609236 | |||||||
| chr19:16609294 | A | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0199 |
3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.72+18578T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609294 | |||||||
| chr19:16609311 | C | CA | 50 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
63 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.72+18560dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | |||||||
| chr19:16609311 | C | CAA | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(11): Show |
19 | HG00621.hp1 HG01884.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.72+18559_72+18560d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | |||||||
| chr19:16609311 | CA | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG01975.hp2 HG03098.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+18560delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | |||||||
| chr19:16609311 | CAAAA | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(10): Show |
20 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.72+18557_72+18560d others(6): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609311 | |||||||
| chr19:16609336 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0086 |
2 | HG04115.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.72+18535_72+18536i others(18): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609336 | |||||||
| chr19:16609336 | A | AAAAAAAA others(8): Show |
8 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG00099.hp1 HG01175.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+18535_72+18536i others(17): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609336 | |||||||
| chr19:16609336 | A | AAAAAAAA others(7): Show |
3 | a0001c0001t0001g0081 a0001c0001t0001g0088 a0001c0006t0001g0082 |
3 | HG00673.hp1 HG02071.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.72+18535_72+18536i others(16): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609336 | |||||||
| chr19:16609418 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.72+18454C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609418 | |||||||
| chr19:16609450 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+18422G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609450 | |||||||
| chr19:16609563 | TTCTTTTC others(519): Show |
T | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+17783_72+18308d others(2): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609563 | |||||||
| chr19:16609567 | T | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+18305A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609567 | |||||||
| chr19:16609826 | T | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+18046A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609826 | |||||||
| chr19:16609827 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02109.hp2 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+18045A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609827 | |||||||
| chr19:16609941 | T | TA | 12 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0032 others(9): Show |
13 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.72+17930dupT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | |||||||
| chr19:16609941 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.72+17921_72+17930d others(12): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | |||||||
| chr19:16609941 | T | TAAAAAAA others(4): Show |
2 | a0001c0001t0001g0064 a0001c0001t0006g0078 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.72+17920_72+17930d others(13): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | |||||||
| chr19:16609941 | TA | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
52 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.72+17930delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | |||||||
| chr19:16609941 | TAA | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(6): Show |
16 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.72+17929_72+17930d others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | |||||||
| chr19:16609941 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.72+17919_72+17930d others(14): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16609941 | |||||||
| chr19:16610039 | T | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(32): Show |
49 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.72+17833A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610039 | |||||||
| chr19:16610082 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.72+17790G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610082 | |||||||
| chr19:16610089 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(30): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+17783C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610089 | |||||||
| chr19:16610188 | A | G | 8 | a0001c0001t0002g0028 a0001c0001t0002g0097 a0001c0001t0002g0098 others(5): Show |
9 | HG01070.hp2 HG01071.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+17684T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610188 | |||||||
| chr19:16610305 | A | C | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+17567T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610305 | |||||||
| chr19:16610317 | A | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+17555T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610317 | |||||||
| chr19:16610340 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0074 |
3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+17532C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610340 | |||||||
| chr19:16610372 | T | G | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+17500A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610372 | |||||||
| chr19:16610394 | CT | C | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0087 others(4): Show |
8 | HG01496.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+17477delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610394 | |||||||
| chr19:16610417 | A | AG | 2 | a0001c0001t0001g0016 a0001c0001t0001g0074 |
3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+17454dupC | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610417 | |||||||
| chr19:16610429 | G | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+17443C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610429 | |||||||
| chr19:16610523 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.72+17349G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610523 | |||||||
| chr19:16610570 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.72+17302A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610570 | |||||||
| chr19:16610870 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+17002C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610870 | |||||||
| chr19:16610987 | A | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0060 a0001c0001t0001g0102 others(1): Show |
9 | HG00280.hp2 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+16885T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16610987 | |||||||
| chr19:16611030 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.72+16842C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611030 | |||||||
| chr19:16611196 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0074 a0001c0001t0001g0075 |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+16676C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611196 | |||||||
| chr19:16611258 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.72+16614C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611258 | |||||||
| chr19:16611395 | TC | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0074 |
3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+16476delG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611395 | |||||||
| chr19:16611474 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
14 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.72+16398A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611474 | |||||||
| chr19:16611497 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.72+16375G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611497 | |||||||
| chr19:16611537 | T | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 others(1): Show |
4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+16335A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611537 | |||||||
| chr19:16611939 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+15933G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16611939 | |||||||
| chr19:16612129 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72+15743G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612129 | |||||||
| chr19:16612137 | C | G | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+15735G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612137 | |||||||
| chr19:16612290 | TG | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
7 | HG00639.hp2 HG01168.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+15581delC | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612290 | |||||||
| chr19:16612663 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.72+15209G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612663 | |||||||
| chr19:16612690 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.72+15182A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612690 | |||||||
| chr19:16612720 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.72+15152C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612720 | |||||||
| chr19:16612729 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+15143C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612729 | |||||||
| chr19:16612772 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
44 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.72+15100T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612772 | |||||||
| chr19:16612818 | C | G | 1 | a0001c0001t0002g0199 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.72+15054G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612818 | |||||||
| chr19:16612834 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.72+15038A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612834 | |||||||
| chr19:16612989 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72+14883G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16612989 | |||||||
| chr19:16613182 | C | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
44 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.72+14690G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613182 | |||||||
| chr19:16613478 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0020 others(24): Show |
34 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.72+14394G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613478 | |||||||
| chr19:16613503 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(30): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+14369G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613503 | |||||||
| chr19:16613593 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.72+14279C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613593 | |||||||
| chr19:16613616 | G | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+14256C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16613616 | |||||||
| chr19:16614023 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0074 |
3 | HG02896.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.72+13849C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614023 | |||||||
| chr19:16614057 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.72+13815G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614057 | |||||||
| chr19:16614270 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+13602C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614270 | |||||||
| chr19:16614344 | A | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 others(1): Show |
4 | HG03098.hp2 HG03471.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+13528T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614344 | |||||||
| chr19:16614376 | A | C | 1 | a0001c0002t0001g0017 | 2 | HG01109.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.72+13496T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614376 | |||||||
| chr19:16614398 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72+13474C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614398 | |||||||
| chr19:16614404 | C | A | 8 | a0001c0001t0002g0028 a0001c0001t0002g0097 a0001c0001t0002g0098 others(5): Show |
9 | HG01070.hp2 HG01071.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+13468G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614404 | |||||||
| chr19:16614558 | G | T | 1 | a0003c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+13314C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614558 | |||||||
| chr19:16614559 | G | C | 1 | a0001c0001t0001g0040 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.72+13313C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614559 | |||||||
| chr19:16614652 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+13220C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614652 | |||||||
| chr19:16614655 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.72+13217C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614655 | |||||||
| chr19:16614700 | G | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.72+13172C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614700 | |||||||
| chr19:16614753 | C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+13119G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614753 | |||||||
| chr19:16614841 | C | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+13031G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16614841 | |||||||
| chr19:16615544 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0148 |
2 | HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.72+12328G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615544 | |||||||
| chr19:16615597 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.72+12275A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615597 | |||||||
| chr19:16615703 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(26): Show |
36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.72+12169T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615703 | |||||||
| chr19:16615753 | GA | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(31): Show |
42 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.72+12118delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16615753 | |||||||
| chr19:16616064 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.72+11808C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616064 | |||||||
| chr19:16616100 | G | C | 1 | a0001c0002t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.72+11772C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616100 | |||||||
| chr19:16616178 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.72+11694C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616178 | |||||||
| chr19:16616207 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(7): Show |
12 | HG01891.hp1 HG01934.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+11665C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616207 | |||||||
| chr19:16616242 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0058 others(1): Show |
7 | HG01884.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+11629delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616242 | |||||||
| chr19:16616318 | A | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(34): Show |
45 | HG00621.hp1 HG01256.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.72+11554T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616318 | |||||||
| chr19:16616380 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.72+11492A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616380 | |||||||
| chr19:16616441 | A | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02015.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.72+11431T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616441 | |||||||
| chr19:16616548 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+11324G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616548 | |||||||
| chr19:16616870 | C | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+11002G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16616870 | |||||||
| chr19:16617086 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+10786G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617086 | |||||||
| chr19:16617157 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72+10715T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617157 | |||||||
| chr19:16617229 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.72+10643T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617229 | |||||||
| chr19:16617230 | G | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.72+10642C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617230 | |||||||
| chr19:16617343 | T | G | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+10529A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617343 | |||||||
| chr19:16617531 | A | G | 5 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0194 others(2): Show |
5 | HG02280.hp2 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+10341T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617531 | |||||||
| chr19:16617569 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.72+10303T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617569 | |||||||
| chr19:16617572 | T | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0108 others(11): Show |
16 | HG00408.hp1 HG00423.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+10300A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617572 | |||||||
| chr19:16617785 | T | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+10087A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617785 | |||||||
| chr19:16617808 | GA | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
129 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.72+10063delT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617808 | |||||||
| chr19:16617911 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72+9961C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617911 | |||||||
| chr19:16617922 | G | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(26): Show |
36 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.72+9950C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16617922 | |||||||
| chr19:16618040 | CT | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0063 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+9831delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618040 | |||||||
| chr19:16618243 | A | G | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG00544.hp1 HG02083.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+9629T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618243 | |||||||
| chr19:16618392 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.72+9480G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618392 | |||||||
| chr19:16618597 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.72+9275T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618597 | |||||||
| chr19:16618685 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.72+9187A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618685 | |||||||
| chr19:16618704 | C | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0035 others(10): Show |
16 | HG00621.hp1 HG01256.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+9168G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618704 | |||||||
| chr19:16618923 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0199 |
3 | HG01070.hp2 HG01071.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.72+8949C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618923 | |||||||
| chr19:16618994 | G | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+8878C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16618994 | |||||||
| chr19:16619008 | GGGCC | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(5): Show |
14 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.72+8860_72+8863del others(4): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619008 | |||||||
| chr19:16619015 | C | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+8857G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619015 | |||||||
| chr19:16619019 | A | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(5): Show |
14 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.72+8853T>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619019 | |||||||
| chr19:16619046 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.72+8826G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619046 | |||||||
| chr19:16619265 | G | A | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+8607C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619265 | |||||||
| chr19:16619324 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(32): Show |
43 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.72+8548A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619324 | |||||||
| chr19:16619327 | A | C | 1 | a0002c0007t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+8545T>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619327 | |||||||
| chr19:16619349 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0139 a0001c0001t0001g0141 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+8523G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619349 | |||||||
| chr19:16619385 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
136 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.72+8487A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619385 | |||||||
| chr19:16619404 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0108 a0001c0001t0001g0109 |
4 | HG03017.hp1 HG03927.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+8468G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619404 | |||||||
| chr19:16619467 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.72+8405C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619467 | |||||||
| chr19:16619758 | G | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+8114C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619758 | |||||||
| chr19:16619967 | C | T | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+7905G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16619967 | |||||||
| chr19:16620008 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.72+7864A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620008 | |||||||
| chr19:16620022 | T | C | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+7850A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620022 | |||||||
| chr19:16620300 | C | T | 12 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(9): Show |
12 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+7572G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620300 | |||||||
| chr19:16620334 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
5 | HG00408.hp1 NA18990.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+7538C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620334 | |||||||
| chr19:16620591 | A | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG00544.hp2 NA18966.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+7281T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620591 | |||||||
| chr19:16620656 | T | C | 1 | a0002c0007t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+7216A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620656 | |||||||
| chr19:16620909 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
7 | HG00639.hp2 HG01168.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+6963G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16620909 | |||||||
| chr19:16621043 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0202 |
2 | NA19006.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.72+6829T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621043 | |||||||
| chr19:16621104 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+6768C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621104 | |||||||
| chr19:16621133 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.72+6739C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621133 | |||||||
| chr19:16621223 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.72+6649A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621223 | |||||||
| chr19:16621237 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.72+6635T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621237 | |||||||
| chr19:16621240 | C | T | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+6632G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621240 | |||||||
| chr19:16621249 | T | C | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+6623A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621249 | |||||||
| chr19:16621517 | A | G | 1 | a0001c0009t0001g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72+6355T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621517 | |||||||
| chr19:16621551 | T | C | 1 | a0002c0007t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+6321A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621551 | |||||||
| chr19:16621872 | C | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0002g0031 |
3 | HG03098.hp2 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.72+6000G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16621872 | |||||||
| chr19:16622291 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.72+5581C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622291 | |||||||
| chr19:16622323 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0067 others(8): Show |
18 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+5549C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622323 | |||||||
| chr19:16622574 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(30): Show |
41 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.72+5298C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622574 | |||||||
| chr19:16622890 | C | A | 7 | a0001c0001t0002g0028 a0001c0001t0002g0194 a0001c0001t0002g0195 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+4982G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16622890 | |||||||
| chr19:16623053 | C | G | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+4819G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623053 | |||||||
| chr19:16623399 | T | C | 2 | a0001c0001t0001g0102 a0003c0008t0001g0092 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.72+4473A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623399 | |||||||
| chr19:16623522 | C | T | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.72+4350G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623522 | |||||||
| chr19:16623684 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.72+4188C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623684 | |||||||
| chr19:16623759 | C | T | 1 | a0002c0007t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+4113G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623759 | |||||||
| chr19:16623762 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0130 a0001c0001t0001g0131 |
4 | HG00609.hp1 HG02040.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+4110G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16623762 | |||||||
| chr19:16624124 | AC | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+3747delG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624124 | |||||||
| chr19:16624125 | C | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0055 others(13): Show |
23 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.72+3747G>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624125 | |||||||
| chr19:16624235 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.72+3637C>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624235 | |||||||
| chr19:16624583 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.72+3289G>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624583 | |||||||
| chr19:16624661 | T | A | 1 | a0001c0005t0003g0077 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+3211A>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624661 | |||||||
| chr19:16624666 | A | G | 2 | a0001c0002t0001g0095 a0001c0002t0001g0096 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.72+3206T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624666 | |||||||
| chr19:16624811 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.72+3061A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624811 | |||||||
| chr19:16624977 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+2895G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16624977 | |||||||
| chr19:16625018 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.72+2854G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625018 | |||||||
| chr19:16625096 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+2776G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625096 | |||||||
| chr19:16625196 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+2676C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625196 | |||||||
| chr19:16625281 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(31): Show |
43 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.72+2591T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625281 | |||||||
| chr19:16625355 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.72+2517C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625355 | |||||||
| chr19:16625415 | G | A | 1 | a0001c0001t0006g0078 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+2457C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625415 | |||||||
| chr19:16625542 | GT | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0068 others(12): Show |
22 | HG01192.hp2 HG01261.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.72+2329delA | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625542 | |||||||
| chr19:16625555 | TC | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+2316delG | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16625555 | |||||||
| chr19:16626018 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG00099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.72+1854A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626018 | |||||||
| chr19:16626326 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG01071.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.72+1546A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626326 | |||||||
| chr19:16626418 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.72+1454A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626418 | |||||||
| chr19:16626565 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+1307G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626565 | |||||||
| chr19:16626644 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0080 others(10): Show |
13 | HG00099.hp1 HG00673.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+1228C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626644 | |||||||
| chr19:16626940 | A | AAC | 12 | a0001c0001t0001g0102 a0001c0001t0002g0031 a0001c0001t0002g0097 others(9): Show |
15 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.72+930_72+931dupGT | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626940 | |||||||
| chr19:16626961 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG01071.hp1 HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.72+911C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16626961 | |||||||
| chr19:16627024 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+848A>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627024 | |||||||
| chr19:16627241 | T | C | 1 | a0003c0008t0001g0092 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+631A>G | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627241 | |||||||
| chr19:16627362 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.72+510C>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627362 | |||||||
| chr19:16627543 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0094 |
5 | HG02257.hp2 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+329C>T | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627543 | |||||||
| chr19:16627558 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(72): Show |
98 | HG00099.hp1 HG00280.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.72+314T>C | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627558 | |||||||
| chr19:16627690 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72+182G>A | MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | 16627690 |