Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5469 |
| ensemblid | ENSG00000125686.12 |
| hgncid | 9234 |
| symbol | MED1 |
| name | mediator complex subunit 1 |
| refseq_nuc | NM_004774.4 |
| refseq_prot | NP_004765.2 |
| ensembl_nuc | ENST00000300651.11 |
| ensembl_prot | ENSP00000300651.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 39404285 |
| end | 39451263 |
| strand | - |
| ver | v1.2 |
| region | chr17:39404285-39451263 |
| region5000 | chr17:39399285-39456263 |
| regionname0 | MED1_chr17_39404285_39451263 |
| regionname5000 | MED1_chr17_39399285_39456263 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1581 | 272 | 79 | 51 | 99 | 13 | 28 | 69 | MED1_chr17_39399285_39456263 | MED1 | MKAQG others(1576): Show |
chr17 | 39399285 | 39456263 |
| a0002 | 0/0 | 1581 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | MKAQG others(1576): Show |
chr17 | 39399285 | 39456263 |
| a0003 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | MKAQG others(1576): Show |
chr17 | 39399285 | 39456263 |
| a0004 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | MKAQG others(1576): Show |
chr17 | 39399285 | 39456263 |
| a0005 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | MKAQG others(1576): Show |
chr17 | 39399285 | 39456263 |
| a0006 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | MKAQG others(1576): Show |
chr17 | 39399285 | 39456263 |
| a0007 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | MKAQG others(1576): Show |
chr17 | 39399285 | 39456263 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4743 | 256 | 66 | 51 | 99 | 12 | 26 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0001c0002 | 0/0 | 4743 | 13 | 11 | 0 | 0 | 1 | 1 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0001c0004 | 0/0 | 4743 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0001c0008 | 0/0 | 4743 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0002c0003 | 0/0 | 4743 | 3 | 3 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0003c0007 | 0/0 | 4743 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0004c0006 | 0/0 | 4743 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0005c0010 | 0/0 | 4743 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0006c0005 | 0/0 | 4743 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 | ||
| a0007c0009 | 0/0 | 4743 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | ATGAA others(4738): Show |
chr17 | 39399285 | 39456263 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8137 | 134 | 24 | 31 | 52 | 7 | 18 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0002 | 0/0 | 8137 | 98 | 35 | 17 | 38 | 4 | 4 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0003 | 0/0 | 8137 | 5 | 0 | 1 | 0 | 1 | 3 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0004 | 0/0 | 8136 | 5 | 5 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8131): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0005 | 0/0 | 8137 | 4 | 0 | 0 | 4 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0006 | 0/0 | 8138 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8133): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0007 | 0/0 | 8138 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8133): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0009 | 0/0 | 8137 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0011 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0012 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0013 | 0/0 | 8137 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0014 | 0/0 | 8137 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0016 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0001t0018 | 0/0 | 8136 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8131): Show |
chr17 | 39399285 | 39456263 |
| a0001c0002t0002 | 0/0 | 8137 | 9 | 9 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0002t0006 | 0/0 | 8138 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8133): Show |
chr17 | 39399285 | 39456263 |
| a0001c0002t0008 | 0/0 | 8137 | 2 | 0 | 0 | 0 | 1 | 1 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0004t0001 | 0/0 | 8137 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0001c0008t0017 | 0/0 | 8137 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0002c0003t0002 | 0/0 | 8137 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0002c0003t0015 | 0/0 | 8137 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0003c0007t0010 | 0/0 | 8138 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8133): Show |
chr17 | 39399285 | 39456263 |
| a0004c0006t0002 | 0/0 | 8137 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0005c0010t0001 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0006c0005t0002 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| a0007c0009t0002 | 0/0 | 8137 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | GAAGT others(8132): Show |
chr17 | 39399285 | 39456263 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0011g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0012g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0013g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0014g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0016g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0001t0018g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0002t0008g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0001c0008t0017g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0002c0003t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0002c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0002c0003t0015g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0003c0007t0010g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0004c0006t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0005c0010t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0006c0005t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| a0007c0009t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | GBR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0202 | EUR | GBR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | FIN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01081 | hp2 | a0003 | c0007 | t0010 | g0007 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01192 | hp2 | a0001 | c0001 | t0014 | g0123 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0236 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01516 | hp1 | a0004 | c0006 | t0002 | g0204 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | IBS | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02004 | hp2 | a0001 | c0001 | t0009 | g0095 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0181 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CDX | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02258 | hp2 | a0002 | c0003 | t0015 | g0271 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02647 | hp1 | a0002 | c0003 | t0002 | g0231 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02738 | hp1 | a0001 | c0002 | t0008 | g0180 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0266 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0275 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0261 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03195 | hp2 | a0002 | c0003 | t0002 | g0272 | AFR | ESN | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0233 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03491 | hp2 | a0001 | c0001 | t0018 | g0061 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03654 | hp1 | a0001 | c0008 | t0017 | g0066 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18961 | hp2 | a0005 | c0010 | t0001 | g0019 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18966 | hp1 | a0006 | c0005 | t0002 | g0195 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18971 | hp2 | a0001 | c0001 | t0011 | g0055 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19006 | hp2 | a0007 | c0009 | t0002 | g0244 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19007 | hp2 | a0001 | c0001 | t0016 | g0248 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19009 | hp1 | a0001 | c0001 | t0012 | g0128 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0179 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0263 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ASW | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20752 | hp2 | a0001 | c0002 | t0008 | g0265 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0174 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | GIH | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0152 | REF | REF | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0223 | REF | REF | MED1_chr17_39399285_39456263 | MED1 | chr17 | 39399285 | 39456263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:39407536 | G | A | 1 | a0003 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.4685C>T | p.Pro1562Leu | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 4886/8137 | 4685/4746 | 1562/1581 | chr17 | 39407536 | |||
| chr17:39408503 | T | C | 1 | a0002 | 3 | HG02258.hp2 HG02647.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.3718A>G | p.Ser1240Gly | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 3919/8137 | 3718/4746 | 1240/1581 | chr17 | 39408503 | |||
| chr17:39409642 | T | A | 1 | a0007 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.2579A>T | p.His860Leu | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2780/8137 | 2579/4746 | 860/1581 | chr17 | 39409642 | |||
| chr17:39410201 | C | T | 1 | a0004 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.2020G>A | p.Gly674Ser | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2221/8137 | 2020/4746 | 674/1581 | chr17 | 39410201 | |||
| chr17:39424721 | T | C | 1 | a0005 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.757A>G | p.Met253Val | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/17 | 958/8137 | 757/4746 | 253/1581 | chr17 | 39424721 | |||
| chr17:39440669 | A | T | 1 | a0006 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.220T>A | p.Leu74Ile | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 4/17 | 421/8137 | 220/4746 | 74/1581 | chr17 | 39440669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:39408117 | G | A | 1 | a0001c0008 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.4104C>T | p.Ser1368Ser | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 4305/8137 | 4104/4746 | 1368/1581 | chr17 | 39408117 | |||
| chr17:39419910 | A | G | 1 | a0001c0002 | 13 | HG02055.hp2 HG02280.hp2 HG02738.hp1 others(10): Show |
synonymous_variant | LOW | c.1104T>C | p.Pro368Pro | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/17 | 1305/8137 | 1104/4746 | 368/1581 | chr17 | 39419910 | |||
| chr17:39423369 | G | A | 1 | a0001c0004 | 2 | HG02055.hp1 HG02145.hp1 |
synonymous_variant | LOW | c.1053C>T | p.Asp351Asp | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/17 | 1254/8137 | 1053/4746 | 351/1581 | chr17 | 39423369 | |||
| chr17:39447900 | T | A | 1 | a0001c0002 | 13 | HG02055.hp2 HG02280.hp2 HG02738.hp1 others(10): Show |
synonymous_variant | LOW | c.30A>T | p.Ser10Ser | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/17 | 231/8137 | 30/4746 | 10/1581 | chr17 | 39447900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:39404520 | T | C | 1 | a0003c0007t0010 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2955A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2955 | chr17 | 39404520 | ||||||
| chr17:39404541 | A | G | 1 | a0002c0003t0015 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2934T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2934 | chr17 | 39404541 | ||||||
| chr17:39404558 | T | C | 1 | a0001c0001t0016 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2917A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2917 | chr17 | 39404558 | ||||||
| chr17:39404611 | G | T | 1 | a0001c0001t0005 | 4 | NA18955.hp1 NA18993.hp2 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2864C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2864 | chr17 | 39404611 | ||||||
| chr17:39404679 | T | C | 1 | a0003c0007t0010 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2796A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2796 | chr17 | 39404679 | ||||||
| chr17:39404878 | C | A | 1 | a0001c0001t0003 | 5 | HG00280.hp2 HG01243.hp2 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2597G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2597 | chr17 | 39404878 | ||||||
| chr17:39405360 | A | G | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(10): Show |
125 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2115T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2115 | chr17 | 39405360 | ||||||
| chr17:39405460 | T | A | 1 | a0001c0001t0001 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2015A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 2015 | chr17 | 39405460 | ||||||
| chr17:39405621 | C | A | 1 | a0001c0008t0017 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1854G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 1854 | chr17 | 39405621 | ||||||
| chr17:39405732 | G | C | 1 | a0001c0001t0012 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 1743 | chr17 | 39405732 | ||||||
| chr17:39405745 | A | G | 1 | a0001c0001t0014 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1730T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 1730 | chr17 | 39405745 | ||||||
| chr17:39405910 | G | T | 1 | a0001c0001t0013 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1565C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 1565 | chr17 | 39405910 | ||||||
| chr17:39406174 | A | G | 2 | a0001c0001t0011 a0001c0001t0012 |
2 | NA18971.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1301T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 1301 | chr17 | 39406174 | ||||||
| chr17:39406559 | C | CT | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0002t0006 others(1): Show |
6 | HG01081.hp2 HG01891.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*915dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 915 | chr17 | 39406559 | ||||||
| chr17:39406559 | CT | C | 2 | a0001c0001t0004 a0001c0001t0018 |
6 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*915delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 915 | chr17 | 39406559 | ||||||
| chr17:39406963 | A | C | 1 | a0001c0001t0009 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 512 | chr17 | 39406963 | ||||||
| chr17:39407314 | G | A | 1 | a0001c0002t0008 | 2 | HG02738.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 17/17 | 161 | chr17 | 39407314 | ||||||
| chr17:39451221 | G | C | 1 | a0001c0001t0001 | 1 | HG02523.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-159C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/17 | chr17 | 39451221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:39410897 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1500-176G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39410897 | |||||||
| chr17:39411188 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0091 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1500-467C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411188 | |||||||
| chr17:39411312 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1500-591G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411312 | |||||||
| chr17:39411374 | A | T | 12 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0181 others(9): Show |
13 | HG02055.hp2 HG02280.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1500-653T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411374 | |||||||
| chr17:39411560 | C | T | 10 | a0001c0001t0002g0168 a0001c0001t0002g0183 a0001c0001t0002g0184 others(7): Show |
10 | HG02109.hp2 HG02486.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1500-839G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411560 | |||||||
| chr17:39411599 | G | C | 1 | a0001c0001t0002g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1500-878C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411599 | |||||||
| chr17:39411721 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0001t0001g0116 others(1): Show |
4 | HG02080.hp2 NA18980.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.1500-1000G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411721 | |||||||
| chr17:39411737 | C | T | 3 | a0002c0003t0002g0231 a0002c0003t0002g0272 a0002c0003t0015g0271 |
3 | HG02258.hp2 HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1500-1016G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411737 | |||||||
| chr17:39411967 | A | G | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1500-1246T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411967 | |||||||
| chr17:39411985 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1500-1264A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39411985 | |||||||
| chr17:39412006 | CA | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1500-1286delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412006 | |||||||
| chr17:39412038 | G | C | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1500-1317C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412038 | |||||||
| chr17:39412228 | C | CT | 19 | a0001c0001t0001g0094 a0001c0001t0002g0153 a0001c0001t0002g0154 others(16): Show |
19 | HG01884.hp1 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1500-1508dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412228 | |||||||
| chr17:39412278 | G | T | 30 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.1500-1557C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412278 | |||||||
| chr17:39412290 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0113 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1500-1569C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412290 | |||||||
| chr17:39412404 | T | C | 5 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1500-1683A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412404 | |||||||
| chr17:39412533 | C | CT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0060 a0001c0001t0001g0120 others(11): Show |
14 | HG00597.hp1 HG01243.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1500-1813dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412533 | |||||||
| chr17:39412533 | CT | C | 14 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(11): Show |
14 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1500-1813delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412533 | |||||||
| chr17:39412537 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0002g0240 a0001c0001t0004g0243 |
3 | HG02976.hp1 HG03453.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1500-1816A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412537 | |||||||
| chr17:39412538 | T | C | 6 | a0001c0001t0002g0173 a0001c0001t0002g0175 a0001c0001t0002g0200 others(3): Show |
6 | HG01496.hp1 HG02015.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1500-1817A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412538 | |||||||
| chr17:39412540 | T | C | 2 | a0001c0001t0004g0158 a0001c0001t0004g0166 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1500-1819A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412540 | |||||||
| chr17:39412822 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1500-2101G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412822 | |||||||
| chr17:39412967 | T | C | 5 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499+2059A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39412967 | |||||||
| chr17:39413178 | A | T | 1 | a0001c0001t0002g0206 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1499+1848T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413178 | |||||||
| chr17:39413257 | T | G | 1 | a0001c0001t0004g0239 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1499+1769A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413257 | |||||||
| chr17:39413268 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1499+1758C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413268 | |||||||
| chr17:39413298 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1499+1728A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413298 | |||||||
| chr17:39413323 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1499+1703G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413323 | |||||||
| chr17:39413468 | G | A | 6 | a0001c0001t0002g0170 a0001c0001t0002g0174 a0001c0001t0002g0207 others(3): Show |
6 | HG00741.hp1 HG01123.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1499+1558C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413468 | |||||||
| chr17:39413734 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1499+1292G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413734 | |||||||
| chr17:39413738 | A | T | 5 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499+1288T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413738 | |||||||
| chr17:39413912 | T | TA | 11 | a0001c0001t0001g0273 a0001c0001t0002g0170 a0001c0001t0002g0174 others(8): Show |
11 | HG00741.hp1 HG01109.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1499+1113dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413912 | |||||||
| chr17:39413912 | TA | T | 53 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0029 others(50): Show |
54 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1499+1113delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413912 | |||||||
| chr17:39413912 | TAA | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(127): Show |
131 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1499+1112_1499+111 others(6): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413912 | |||||||
| chr17:39413965 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1499+1061C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39413965 | |||||||
| chr17:39414120 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1499+906T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414120 | |||||||
| chr17:39414253 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1499+773A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414253 | |||||||
| chr17:39414286 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1499+740G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414286 | |||||||
| chr17:39414338 | A | AT | 5 | a0001c0001t0001g0045 a0001c0001t0001g0115 a0001c0001t0002g0215 others(2): Show |
5 | HG00741.hp1 HG01515.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499+687dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414338 | |||||||
| chr17:39414370 | C | G | 1 | a0001c0001t0001g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1499+656G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414370 | |||||||
| chr17:39414484 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1499+542G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414484 | |||||||
| chr17:39414525 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1499+501G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414525 | |||||||
| chr17:39414571 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1499+455C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414571 | |||||||
| chr17:39414614 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1499+412G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414614 | |||||||
| chr17:39414626 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1499+400C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414626 | |||||||
| chr17:39414634 | C | CT | 27 | a0001c0001t0002g0002 a0001c0001t0002g0170 a0001c0001t0002g0171 others(24): Show |
28 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1499+391dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | C | CTT | 8 | a0001c0001t0002g0175 a0001c0001t0002g0200 a0001c0001t0002g0203 others(5): Show |
8 | HG00597.hp2 HG00621.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1499+390_1499+391d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | C | CTTTCTTT others(3): Show |
1 | a0001c0001t0002g0169 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1499+391_1499+392i others(12): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CT | C | 10 | a0001c0001t0002g0183 a0001c0001t0002g0185 a0001c0001t0002g0186 others(7): Show |
10 | HG02129.hp1 HG02818.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1499+391delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTT | C | 10 | a0001c0001t0001g0177 a0001c0001t0001g0260 a0001c0001t0002g0229 others(7): Show |
10 | HG01070.hp2 HG01258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1499+390_1499+391d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTT | C | 6 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0001t0002g0157 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1499+388_1499+391d others(6): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTT | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0140 others(3): Show |
6 | HG02071.hp2 HG02080.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1499+386_1499+391d others(8): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0029 others(14): Show |
17 | HG00639.hp1 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1499+385_1499+391d others(9): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(1): Show |
C | 73 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0020 others(70): Show |
73 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1499+384_1499+391d others(10): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(2): Show |
C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0023 others(51): Show |
55 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.1499+383_1499+391d others(11): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0007g0010 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1499+382_1499+391d others(12): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0247 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1499+381_1499+391d others(13): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0002g0003 a0001c0001t0002g0199 a0001c0001t0002g0201 others(3): Show |
7 | HG00423.hp2 HG01346.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499+380_1499+391d others(14): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0002g0004 a0001c0001t0002g0194 a0001c0001t0002g0213 others(3): Show |
7 | HG00738.hp2 HG01943.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499+379_1499+391d others(15): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0002g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1499+378_1499+391d others(16): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0162 others(3): Show |
6 | HG02451.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499+377_1499+391d others(17): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0002g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1499+374_1499+391d others(20): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0002g0258 a0001c0002t0006g0179 a0001c0002t0008g0180 |
3 | HG02145.hp2 HG02738.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1499+372_1499+391d others(22): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414634 | CTTTTTTT others(14): Show |
C | 15 | a0001c0001t0002g0240 a0001c0001t0002g0254 a0001c0001t0002g0255 others(12): Show |
16 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1499+371_1499+391d others(23): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414634 | |||||||
| chr17:39414674 | T | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1499+352A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414674 | |||||||
| chr17:39414733 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1499+293T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414733 | |||||||
| chr17:39414774 | AT | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0119 a0001c0001t0001g0134 |
3 | HG02056.hp2 HG02135.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1499+251delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414774 | |||||||
| chr17:39414818 | C | T | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1499+208G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414818 | |||||||
| chr17:39414950 | G | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1499+76C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | 39414950 | |||||||
| chr17:39415402 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1298-63C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415402 | |||||||
| chr17:39415574 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0091 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1298-235C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415574 | |||||||
| chr17:39415595 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1298-256C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415595 | |||||||
| chr17:39415598 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1298-259C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415598 | |||||||
| chr17:39415627 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1298-288T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415627 | |||||||
| chr17:39415672 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1298-333A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415672 | |||||||
| chr17:39415674 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1298-335C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415674 | |||||||
| chr17:39415677 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1298-338G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415677 | |||||||
| chr17:39415710 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1298-371C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415710 | |||||||
| chr17:39415756 | G | A | 26 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0037 others(23): Show |
26 | HG01106.hp1 HG01123.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1298-417C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415756 | |||||||
| chr17:39415779 | T | C | 2 | a0001c0001t0004g0158 a0001c0001t0004g0166 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1298-440A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415779 | |||||||
| chr17:39415814 | C | CA | 20 | a0001c0001t0001g0056 a0001c0001t0001g0177 a0001c0001t0001g0178 others(17): Show |
20 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1298-476dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415814 | |||||||
| chr17:39415814 | CA | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1298-476delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415814 | |||||||
| chr17:39415814 | CAA | C | 7 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0001t0002g0157 others(4): Show |
7 | HG02559.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1298-477_1298-476d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415814 | |||||||
| chr17:39415886 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1298-547C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415886 | |||||||
| chr17:39415989 | C | CA | 16 | a0001c0001t0002g0217 a0001c0001t0002g0245 a0001c0001t0002g0246 others(13): Show |
17 | HG00621.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1298-651dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39415989 | |||||||
| chr17:39416074 | C | T | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1298-735G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39416074 | |||||||
| chr17:39416299 | C | G | 1 | a0001c0001t0001g0011 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1298-960G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39416299 | |||||||
| chr17:39416812 | A | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(192): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1298-1473T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39416812 | |||||||
| chr17:39416893 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1298-1554G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39416893 | |||||||
| chr17:39416943 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1298-1604C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39416943 | |||||||
| chr17:39417074 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1298-1735A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417074 | |||||||
| chr17:39417192 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1298-1853A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417192 | |||||||
| chr17:39417193 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(142): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1298-1854C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417193 | |||||||
| chr17:39417263 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1298-1924T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417263 | |||||||
| chr17:39417329 | C | CA | 18 | a0001c0001t0001g0065 a0001c0001t0002g0153 a0001c0001t0002g0154 others(15): Show |
18 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1298-1991dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417329 | |||||||
| chr17:39417425 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1298-2086C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417425 | |||||||
| chr17:39417469 | A | G | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1298-2130T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417469 | |||||||
| chr17:39417521 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1298-2182G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417521 | |||||||
| chr17:39417588 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1297+2129G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417588 | |||||||
| chr17:39417615 | C | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02602.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1297+2102G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417615 | |||||||
| chr17:39417654 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1297+2063A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417654 | |||||||
| chr17:39417842 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1297+1875G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417842 | |||||||
| chr17:39417917 | G | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297+1800C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417917 | |||||||
| chr17:39417962 | A | C | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1297+1755T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417962 | |||||||
| chr17:39417989 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1297+1728G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39417989 | |||||||
| chr17:39418014 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1297+1703T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418014 | |||||||
| chr17:39418029 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1297+1688A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418029 | |||||||
| chr17:39418085 | C | CA | 25 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0002g0153 others(22): Show |
25 | HG00140.hp2 HG00673.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1297+1631dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418085 | |||||||
| chr17:39418085 | C | CAA | 11 | a0001c0001t0001g0069 a0001c0001t0001g0131 a0001c0001t0002g0160 others(8): Show |
12 | HG01516.hp2 HG01517.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297+1630_1297+163 others(6): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418085 | |||||||
| chr17:39418085 | C | CAAA | 87 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(84): Show |
88 | HG00280.hp1 HG00597.hp1 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.1297+1629_1297+163 others(7): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418085 | |||||||
| chr17:39418085 | C | CAAAA | 50 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0027 others(47): Show |
50 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1297+1628_1297+163 others(8): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418085 | |||||||
| chr17:39418085 | C | CAAAAA | 13 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0034 others(10): Show |
13 | HG00741.hp2 HG01071.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1297+1627_1297+163 others(9): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418085 | |||||||
| chr17:39418311 | A | C | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297+1406T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418311 | |||||||
| chr17:39418339 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0137 |
2 | HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1297+1378C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418339 | |||||||
| chr17:39418356 | T | TAG | 143 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(140): Show |
144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1297+1359_1297+136 others(6): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418356 | |||||||
| chr17:39418410 | A | G | 8 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(5): Show |
8 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297+1307T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418410 | |||||||
| chr17:39418436 | G | C | 1 | a0001c0001t0004g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1297+1281C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418436 | |||||||
| chr17:39418469 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1297+1248C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418469 | |||||||
| chr17:39418525 | C | T | 2 | a0001c0001t0002g0168 a0001c0001t0002g0187 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1297+1192G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418525 | |||||||
| chr17:39418682 | A | C | 1 | a0001c0001t0001g0259 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1297+1035T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418682 | |||||||
| chr17:39418724 | A | C | 1 | a0001c0002t0002g0266 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1297+993T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418724 | |||||||
| chr17:39418762 | T | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1297+955A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418762 | |||||||
| chr17:39418789 | A | AT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(139): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1297+927dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418789 | |||||||
| chr17:39418789 | A | ATT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0120 others(4): Show |
7 | HG00741.hp2 HG02056.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1297+926_1297+927d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418789 | |||||||
| chr17:39418977 | TG | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0139 |
3 | HG01346.hp2 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1297+739delC | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39418977 | |||||||
| chr17:39419065 | A | G | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1297+652T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39419065 | |||||||
| chr17:39419410 | A | AT | 19 | a0001c0001t0002g0155 a0001c0001t0002g0240 a0001c0001t0002g0254 others(16): Show |
20 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1297+306dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39419410 | |||||||
| chr17:39419421 | T | C | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297+296A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39419421 | |||||||
| chr17:39419428 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1297+289C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39419428 | |||||||
| chr17:39419452 | G | A | 30 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.1297+265C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39419452 | |||||||
| chr17:39419516 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(146): Show |
150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1297+201A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39419516 | |||||||
| chr17:39419601 | A | G | 17 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0002g0153 others(14): Show |
17 | HG01109.hp2 HG02451.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1297+116T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 14/16 | chr17 | 39419601 | |||||||
| chr17:39419962 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0135 |
3 | HG02132.hp1 NA18971.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1096-44A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39419962 | |||||||
| chr17:39420164 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1096-246A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420164 | |||||||
| chr17:39420197 | C | CT | 9 | a0001c0001t0001g0068 a0001c0001t0001g0126 a0001c0001t0001g0130 others(6): Show |
9 | HG00423.hp1 HG00673.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096-280dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420197 | |||||||
| chr17:39420197 | CT | C | 17 | a0001c0001t0001g0038 a0001c0001t0001g0086 a0001c0001t0001g0119 others(14): Show |
17 | HG00741.hp1 HG01081.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.1096-280delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420197 | |||||||
| chr17:39420293 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1096-375C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420293 | |||||||
| chr17:39420302 | C | A | 1 | a0001c0001t0013g0233 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1096-384G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420302 | |||||||
| chr17:39420505 | A | G | 1 | a0001c0008t0017g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1096-587T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420505 | |||||||
| chr17:39420622 | C | T | 1 | a0001c0001t0004g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1096-704G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420622 | |||||||
| chr17:39420791 | A | AT | 161 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
163 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1096-874dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420791 | |||||||
| chr17:39420791 | A | ATT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0133 others(3): Show |
6 | HG00741.hp2 HG02293.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-875_1096-874d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420791 | |||||||
| chr17:39420791 | ATT | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-875_1096-874d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420791 | |||||||
| chr17:39420859 | G | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0227 |
2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1096-941C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420859 | |||||||
| chr17:39420859 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1096-941C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420859 | |||||||
| chr17:39420870 | G | A | 15 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(12): Show |
15 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1096-952C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420870 | |||||||
| chr17:39420931 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1096-1013C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39420931 | |||||||
| chr17:39421033 | T | G | 1 | a0001c0001t0016g0248 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1096-1115A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421033 | |||||||
| chr17:39421066 | G | C | 1 | a0001c0001t0002g0171 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1096-1148C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421066 | |||||||
| chr17:39421075 | C | T | 8 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(5): Show |
8 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-1157G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421075 | |||||||
| chr17:39421085 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1096-1167G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421085 | |||||||
| chr17:39421091 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1096-1173G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421091 | |||||||
| chr17:39421206 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1096-1288C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421206 | |||||||
| chr17:39421238 | C | CA | 17 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(14): Show |
17 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1096-1321dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421238 | |||||||
| chr17:39421246 | AAAAAAAG | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1096-1335_1096-132 others(11): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421246 | |||||||
| chr17:39421499 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1096-1581C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421499 | |||||||
| chr17:39421559 | T | TA | 14 | a0001c0001t0001g0015 a0001c0001t0001g0037 a0001c0001t0001g0057 others(11): Show |
14 | HG01106.hp1 HG01123.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1096-1642dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421559 | |||||||
| chr17:39421848 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1095+1479C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421848 | |||||||
| chr17:39421848 | G | T | 1 | a0001c0001t0013g0233 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1095+1479C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421848 | |||||||
| chr17:39421866 | C | A | 4 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095+1461G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421866 | |||||||
| chr17:39421903 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1095+1424G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39421903 | |||||||
| chr17:39422127 | CA | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1095+1199delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422127 | |||||||
| chr17:39422181 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1095+1146A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422181 | |||||||
| chr17:39422391 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1095+936G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422391 | |||||||
| chr17:39422445 | A | G | 17 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(14): Show |
17 | HG01081.hp2 HG02451.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1095+882T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422445 | |||||||
| chr17:39422469 | G | GT | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(54): Show |
57 | HG00423.hp2 HG01081.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1095+857dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422469 | |||||||
| chr17:39422469 | G | GTT | 5 | a0001c0001t0001g0078 a0001c0001t0001g0120 a0001c0001t0002g0153 others(2): Show |
5 | HG02886.hp1 HG03209.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+856_1095+857d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422469 | |||||||
| chr17:39422576 | A | G | 2 | a0001c0001t0002g0240 a0001c0001t0004g0243 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1095+751T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422576 | |||||||
| chr17:39422863 | C | CT | 80 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0022 others(77): Show |
80 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1095+463dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422863 | |||||||
| chr17:39422863 | C | CTT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(63): Show |
67 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.1095+462_1095+463d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422863 | |||||||
| chr17:39422863 | CT | C | 5 | a0001c0001t0002g0183 a0001c0001t0002g0186 a0001c0001t0002g0220 others(2): Show |
5 | HG01081.hp2 HG02155.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1095+463delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422863 | |||||||
| chr17:39422870 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1095+457A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422870 | |||||||
| chr17:39422896 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0146 |
2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1095+431G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39422896 | |||||||
| chr17:39423014 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0146 |
2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1095+313G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39423014 | |||||||
| chr17:39423130 | G | A | 9 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0086 others(6): Show |
9 | HG00280.hp2 HG01243.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1095+197C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39423130 | |||||||
| chr17:39423189 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1095+138G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 13/16 | chr17 | 39423189 | |||||||
| chr17:39423831 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.852-10T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39423831 | |||||||
| chr17:39423950 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.852-129A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39423950 | |||||||
| chr17:39424032 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.852-211C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39424032 | |||||||
| chr17:39424043 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.852-222G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39424043 | |||||||
| chr17:39424162 | C | T | 2 | a0001c0001t0002g0155 a0001c0001t0002g0165 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.852-341G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39424162 | |||||||
| chr17:39424185 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.852-364T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39424185 | |||||||
| chr17:39424226 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.851+401T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39424226 | |||||||
| chr17:39424451 | C | T | 30 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.851+176G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 11/16 | chr17 | 39424451 | |||||||
| chr17:39424777 | T | C | 3 | a0001c0001t0002g0155 a0001c0001t0002g0165 a0001c0001t0002g0167 |
3 | HG03130.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.740-39A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39424777 | |||||||
| chr17:39424879 | G | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.740-141C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39424879 | |||||||
| chr17:39424902 | CAG | C | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.740-166_740-165del others(2): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39424902 | |||||||
| chr17:39425100 | C | T | 30 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.740-362G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425100 | |||||||
| chr17:39425116 | T | G | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.740-378A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425116 | |||||||
| chr17:39425183 | G | A | 8 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(5): Show |
8 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.740-445C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425183 | |||||||
| chr17:39425260 | G | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.740-522C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425260 | |||||||
| chr17:39425337 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.740-599A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425337 | |||||||
| chr17:39425530 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.740-792C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425530 | |||||||
| chr17:39425552 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.740-814G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425552 | |||||||
| chr17:39425619 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.740-881G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425619 | |||||||
| chr17:39425804 | G | GA | 14 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0140 others(11): Show |
14 | HG00423.hp1 HG00621.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.740-1067dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425804 | |||||||
| chr17:39425804 | GA | G | 31 | a0001c0001t0001g0087 a0001c0001t0001g0177 a0001c0001t0001g0178 others(28): Show |
32 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.740-1067delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425804 | |||||||
| chr17:39425806 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.740-1068T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425806 | |||||||
| chr17:39425986 | G | T | 1 | a0001c0001t0002g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.740-1248C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39425986 | |||||||
| chr17:39426115 | A | G | 15 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(12): Show |
15 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.740-1377T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426115 | |||||||
| chr17:39426132 | G | C | 3 | a0001c0002t0002g0264 a0001c0002t0006g0179 a0001c0002t0006g0275 |
3 | HG02809.hp1 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.740-1394C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426132 | |||||||
| chr17:39426301 | G | C | 15 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(12): Show |
15 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.739+1400C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426301 | |||||||
| chr17:39426403 | C | T | 2 | a0001c0001t0004g0158 a0001c0001t0004g0166 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.739+1298G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426403 | |||||||
| chr17:39426424 | G | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.739+1277C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426424 | |||||||
| chr17:39426458 | T | C | 10 | a0001c0001t0002g0168 a0001c0001t0002g0183 a0001c0001t0002g0184 others(7): Show |
10 | HG02109.hp2 HG02486.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.739+1243A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426458 | |||||||
| chr17:39426462 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.739+1239G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426462 | |||||||
| chr17:39426691 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.739+1010G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426691 | |||||||
| chr17:39426793 | C | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.739+908G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426793 | |||||||
| chr17:39426809 | C | G | 1 | a0006c0005t0002g0195 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.739+892G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426809 | |||||||
| chr17:39426825 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0065 |
2 | NA18975.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.739+876G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426825 | |||||||
| chr17:39426826 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.739+875C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39426826 | |||||||
| chr17:39427076 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.739+625T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427076 | |||||||
| chr17:39427212 | C | T | 3 | a0001c0001t0002g0209 a0001c0001t0002g0214 a0001c0001t0002g0218 |
3 | NA18987.hp2 NA18993.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.739+489G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427212 | |||||||
| chr17:39427324 | G | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.739+377C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427324 | |||||||
| chr17:39427328 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.739+373G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427328 | |||||||
| chr17:39427470 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0119 a0001c0001t0001g0134 |
3 | HG02056.hp2 HG02135.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.739+231C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427470 | |||||||
| chr17:39427526 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.739+175A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427526 | |||||||
| chr17:39427619 | C | G | 15 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(12): Show |
15 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.739+82G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427619 | |||||||
| chr17:39427662 | C | T | 1 | a0001c0002t0008g0265 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.739+39G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 10/16 | chr17 | 39427662 | |||||||
| chr17:39428039 | AGACTCCA others(110): Show |
A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | NA18964.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.650-366_650-250del | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39428039 | |||||||
| chr17:39428115 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(190): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.650-325T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39428115 | |||||||
| chr17:39428479 | G | A | 3 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0258 |
3 | HG02145.hp2 HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.650-689C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39428479 | |||||||
| chr17:39428754 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.650-964C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39428754 | |||||||
| chr17:39428877 | A | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.650-1087T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39428877 | |||||||
| chr17:39429185 | C | T | 5 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-1395G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429185 | |||||||
| chr17:39429681 | G | A | 15 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(12): Show |
15 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.649+1434C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429681 | |||||||
| chr17:39429702 | T | TA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(136): Show |
140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.649+1412dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429702 | |||||||
| chr17:39429702 | T | TAA | 34 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0032 others(31): Show |
34 | HG00621.hp2 HG01070.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.649+1411_649+1412d others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429702 | |||||||
| chr17:39429702 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0002g0270 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.649+1403_649+1412d others(12): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429702 | |||||||
| chr17:39429901 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.649+1214A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429901 | |||||||
| chr17:39429915 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.649+1200G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39429915 | |||||||
| chr17:39430394 | C | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.649+721G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430394 | |||||||
| chr17:39430541 | A | C | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.649+574T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430541 | |||||||
| chr17:39430603 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.649+512C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430603 | |||||||
| chr17:39430650 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.649+465C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430650 | |||||||
| chr17:39430688 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.649+427C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430688 | |||||||
| chr17:39430692 | TA | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(184): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.649+422delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430692 | |||||||
| chr17:39430744 | G | A | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.649+371C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430744 | |||||||
| chr17:39430927 | G | A | 16 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(13): Show |
16 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.649+188C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430927 | |||||||
| chr17:39430967 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.649+148G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 9/16 | chr17 | 39430967 | |||||||
| chr17:39431281 | CT | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(162): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.576-94delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 8/16 | chr17 | 39431281 | |||||||
| chr17:39431288 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0120 |
3 | HG02683.hp2 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.576-100A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 8/16 | chr17 | 39431288 | |||||||
| chr17:39431354 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.576-166G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 8/16 | chr17 | 39431354 | |||||||
| chr17:39432069 | C | T | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.501-53G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432069 | |||||||
| chr17:39432342 | C | CA | 18 | a0001c0001t0001g0015 a0001c0001t0001g0059 a0001c0001t0001g0083 others(15): Show |
18 | HG02071.hp1 HG02135.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.501-327dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432342 | |||||||
| chr17:39432342 | C | CAA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(178): Show |
183 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.501-328_501-327dup others(2): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432342 | |||||||
| chr17:39432405 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.501-389A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432405 | |||||||
| chr17:39432474 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(142): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.501-458C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432474 | |||||||
| chr17:39432647 | G | A | 16 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(13): Show |
16 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.501-631C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432647 | |||||||
| chr17:39432740 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.501-724C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432740 | |||||||
| chr17:39432753 | C | CA | 5 | a0001c0001t0001g0090 a0001c0001t0001g0142 a0001c0001t0002g0214 others(2): Show |
5 | HG01981.hp1 HG02145.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-738dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432753 | |||||||
| chr17:39432790 | C | T | 16 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(13): Show |
16 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.501-774G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432790 | |||||||
| chr17:39432808 | T | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.501-792A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432808 | |||||||
| chr17:39432830 | C | T | 30 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0260 others(27): Show |
31 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.501-814G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432830 | |||||||
| chr17:39432870 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.501-854C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39432870 | |||||||
| chr17:39433111 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(145): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.501-1095C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433111 | |||||||
| chr17:39433152 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.500+1097C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433152 | |||||||
| chr17:39433168 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0116 a0001c0001t0001g0125 |
3 | HG02080.hp2 NA18980.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.500+1081T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433168 | |||||||
| chr17:39433182 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0165 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.500+1067C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433182 | |||||||
| chr17:39433233 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500+1016C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433233 | |||||||
| chr17:39433370 | A | T | 1 | a0001c0001t0013g0233 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.500+879T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433370 | |||||||
| chr17:39433379 | G | GA | 6 | a0001c0001t0001g0122 a0001c0001t0001g0274 a0001c0001t0002g0193 others(3): Show |
6 | HG02630.hp1 HG03831.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.500+869dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433379 | |||||||
| chr17:39433527 | C | CTA | 47 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0082 others(44): Show |
50 | HG00423.hp2 HG00738.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.500+720_500+721dup others(2): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433527 | |||||||
| chr17:39433527 | C | CTATA | 8 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0112 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.500+718_500+721dup others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433527 | |||||||
| chr17:39433527 | C | CTATATAT others(1): Show |
7 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(4): Show |
7 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.500+714_500+721dup others(8): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433527 | |||||||
| chr17:39433527 | C | CTATATAT others(3): Show |
4 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0001t0002g0157 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+712_500+721dup others(10): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433527 | |||||||
| chr17:39433527 | C | CTATATAT others(11): Show |
1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.500+704_500+721dup others(18): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433527 | |||||||
| chr17:39433536 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.500+713A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433536 | |||||||
| chr17:39433546 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | NA18964.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.500+703A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433546 | |||||||
| chr17:39433546 | T | TAC | 3 | a0001c0001t0001g0049 a0001c0001t0001g0086 a0001c0001t0001g0274 |
3 | HG01993.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.500+701_500+702dup others(2): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433546 | |||||||
| chr17:39433546 | T | TATATATA others(19): Show |
1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.500+702_500+703ins others(26): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39433546 | |||||||
| chr17:39434003 | A | G | 1 | a0001c0002t0002g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.500+246T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39434003 | |||||||
| chr17:39434018 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.500+231G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 7/16 | chr17 | 39434018 | |||||||
| chr17:39434327 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.429-7C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39434327 | |||||||
| chr17:39434688 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0086 |
2 | HG01993.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.429-368C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39434688 | |||||||
| chr17:39434896 | G | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(142): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.429-576C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39434896 | |||||||
| chr17:39434946 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.429-626T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39434946 | |||||||
| chr17:39435036 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.429-716G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435036 | |||||||
| chr17:39435100 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.429-780C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435100 | |||||||
| chr17:39435169 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.429-849T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435169 | |||||||
| chr17:39435173 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.429-853T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435173 | |||||||
| chr17:39435362 | G | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.429-1042C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435362 | |||||||
| chr17:39435422 | T | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.429-1102A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435422 | |||||||
| chr17:39435424 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429-1104A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435424 | |||||||
| chr17:39435543 | C | A | 7 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(4): Show |
7 | HG02451.hp1 HG02559.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.429-1223G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435543 | |||||||
| chr17:39435610 | G | A | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.429-1290C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435610 | |||||||
| chr17:39435794 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.429-1474A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39435794 | |||||||
| chr17:39436258 | G | A | 3 | a0001c0001t0001g0012 a0001c0004t0001g0013 a0001c0004t0001g0014 |
3 | HG02055.hp1 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.429-1938C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436258 | |||||||
| chr17:39436292 | C | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.429-1972G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436292 | |||||||
| chr17:39436346 | G | A | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.429-2026C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436346 | |||||||
| chr17:39436348 | A | G | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.429-2028T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436348 | |||||||
| chr17:39436369 | GA | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(149): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.429-2050delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436369 | |||||||
| chr17:39436467 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.429-2147G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436467 | |||||||
| chr17:39436768 | T | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.428+2397A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436768 | |||||||
| chr17:39436885 | A | C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0259 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+2280T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436885 | |||||||
| chr17:39436888 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.428+2277G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436888 | |||||||
| chr17:39436906 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.428+2259A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436906 | |||||||
| chr17:39436911 | G | A | 2 | a0001c0001t0001g0085 a0001c0002t0008g0265 |
2 | NA18966.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.428+2254C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436911 | |||||||
| chr17:39436924 | T | A | 4 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+2241A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39436924 | |||||||
| chr17:39437066 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0086 |
2 | HG01993.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.428+2099C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437066 | |||||||
| chr17:39437152 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.428+2013C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437152 | |||||||
| chr17:39437184 | G | A | 12 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0259 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.428+1981C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437184 | |||||||
| chr17:39437398 | G | C | 1 | a0001c0001t0002g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.428+1767C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437398 | |||||||
| chr17:39437488 | C | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0062 others(3): Show |
6 | HG01192.hp2 HG01346.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+1677G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437488 | |||||||
| chr17:39437549 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.428+1616T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437549 | |||||||
| chr17:39437622 | G | GA | 17 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(14): Show |
17 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.428+1542dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437622 | |||||||
| chr17:39437805 | A | G | 5 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+1360T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437805 | |||||||
| chr17:39437851 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.428+1314A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437851 | |||||||
| chr17:39437872 | T | C | 8 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(5): Show |
8 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+1293A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437872 | |||||||
| chr17:39437999 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.428+1166G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39437999 | |||||||
| chr17:39438041 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.428+1124C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438041 | |||||||
| chr17:39438173 | A | AT | 19 | a0001c0001t0001g0138 a0001c0001t0002g0153 a0001c0001t0002g0154 others(16): Show |
19 | HG02056.hp1 HG02451.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.428+991dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438173 | |||||||
| chr17:39438337 | A | AT | 16 | a0001c0001t0002g0168 a0001c0001t0002g0189 a0001c0001t0002g0192 others(13): Show |
16 | HG00140.hp2 HG00741.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.428+827dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438337 | |||||||
| chr17:39438337 | AT | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(146): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.428+827delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438337 | |||||||
| chr17:39438337 | ATT | A | 26 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0259 others(23): Show |
26 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.428+826_428+827del others(2): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438337 | |||||||
| chr17:39438383 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.428+782C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438383 | |||||||
| chr17:39438709 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.428+456A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438709 | |||||||
| chr17:39438806 | G | T | 25 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
25 | HG00280.hp1 HG00621.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.428+359C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438806 | |||||||
| chr17:39438886 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.428+279A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438886 | |||||||
| chr17:39438960 | G | A | 2 | a0001c0001t0002g0168 a0001c0001t0002g0187 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.428+205C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 6/16 | chr17 | 39438960 | |||||||
| chr17:39439371 | T | G | 1 | a0001c0001t0002g0213 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.400-178A>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439371 | |||||||
| chr17:39439825 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.399+561G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439825 | |||||||
| chr17:39439919 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.399+467G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439919 | |||||||
| chr17:39439965 | G | GGAAA | 3 | a0001c0001t0002g0155 a0001c0001t0002g0165 a0001c0001t0002g0167 |
3 | HG03130.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.399+417_399+420dup others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439965 | |||||||
| chr17:39439965 | GGAAA | G | 15 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0002g0182 others(12): Show |
16 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.399+417_399+420del others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439965 | |||||||
| chr17:39439981 | A | AGAAG | 6 | a0001c0001t0002g0172 a0001c0001t0002g0254 a0001c0001t0002g0255 others(3): Show |
6 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.399+404_399+405ins others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439981 | |||||||
| chr17:39439981 | AGAAAGAA others(1): Show |
A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
14 | HG00280.hp1 HG00621.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.399+397_399+404del others(8): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439981 | |||||||
| chr17:39439985 | A | AGAAG | 24 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0065 others(21): Show |
24 | HG00140.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.399+397_399+400dup others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439985 | |||||||
| chr17:39439985 | A | AGAAGGAA others(1): Show |
6 | a0001c0001t0001g0259 a0001c0001t0002g0184 a0001c0001t0002g0186 others(3): Show |
6 | HG01361.hp1 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+393_399+400dup others(8): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439985 | |||||||
| chr17:39439985 | A | AGAAGGAA others(5): Show |
3 | a0001c0001t0002g0238 a0001c0001t0002g0250 a0001c0001t0002g0257 |
3 | HG01109.hp1 HG02132.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.399+389_399+400dup others(12): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439985 | |||||||
| chr17:39439985 | A | AGAAGGAA others(9): Show |
5 | a0001c0001t0001g0260 a0001c0001t0002g0251 a0001c0001t0002g0252 others(2): Show |
5 | HG01258.hp1 NA18975.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+385_399+400dup others(16): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439985 | |||||||
| chr17:39439985 | A | G | 9 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0172 others(6): Show |
9 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+401T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439985 | |||||||
| chr17:39439985 | AGAAG | A | 11 | a0001c0001t0001g0052 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG00738.hp1 HG01109.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+397_399+400del others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439985 | |||||||
| chr17:39439989 | G | A | 5 | a0001c0001t0002g0154 a0001c0001t0002g0156 a0001c0001t0002g0157 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+397C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39439989 | |||||||
| chr17:39440005 | GGAAGGAA others(9): Show |
G | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.399+365_399+380del others(16): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440005 | |||||||
| chr17:39440009 | GGAAGGAA others(5): Show |
G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG02602.hp2 HG04204.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+365_399+376del others(12): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440009 | |||||||
| chr17:39440013 | GGAAGGAA others(1): Show |
G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG02809.hp2 HG03834.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+365_399+372del others(8): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440013 | |||||||
| chr17:39440017 | GGAAA | G | 44 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(41): Show |
44 | HG00280.hp2 HG00639.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.399+365_399+368del others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440017 | |||||||
| chr17:39440019 | A | AAGGAAGG others(8): Show |
1 | a0001c0001t0002g0249 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.399+366_399+367ins others(15): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440019 | |||||||
| chr17:39440021 | A | G | 35 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(32): Show |
35 | HG00280.hp1 HG00621.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.399+365T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440021 | |||||||
| chr17:39440023 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.399+363T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440023 | |||||||
| chr17:39440025 | A | G | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.399+361T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440025 | |||||||
| chr17:39440032 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01952.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.399+354T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440032 | |||||||
| chr17:39440036 | G | A | 2 | a0001c0001t0002g0172 a0003c0007t0010g0007 |
2 | HG01081.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.399+350C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440036 | |||||||
| chr17:39440040 | A | G | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.399+346T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440040 | |||||||
| chr17:39440044 | G | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.399+342C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440044 | |||||||
| chr17:39440046 | A | G | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.399+340T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440046 | |||||||
| chr17:39440073 | AAAGC | A | 3 | a0001c0001t0004g0158 a0001c0001t0004g0166 a0003c0007t0010g0007 |
3 | HG01081.hp2 HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.399+309_399+312del others(4): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440073 | |||||||
| chr17:39440089 | C | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.399+297G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440089 | |||||||
| chr17:39440125 | A | G | 1 | a0001c0002t0002g0261 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.399+261T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440125 | |||||||
| chr17:39440181 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(267): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.399+205A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440181 | |||||||
| chr17:39440282 | T | A | 12 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0259 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.399+104A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440282 | |||||||
| chr17:39440317 | C | G | 1 | a0001c0001t0011g0055 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.399+69G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | 39440317 | |||||||
| chr17:39440601 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.266+22A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 4/16 | chr17 | 39440601 | |||||||
| chr17:39440845 | G | A | 8 | a0001c0001t0002g0193 a0001c0001t0002g0249 a0001c0001t0002g0250 others(5): Show |
8 | HG02129.hp1 HG02132.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-168C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39440845 | |||||||
| chr17:39440932 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(192): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.212-255T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39440932 | |||||||
| chr17:39441085 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0091 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-408C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441085 | |||||||
| chr17:39441237 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0139 |
3 | HG01346.hp2 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.212-560T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441237 | |||||||
| chr17:39441285 | G | A | 12 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0259 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.212-608C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441285 | |||||||
| chr17:39441495 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.212-818G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441495 | |||||||
| chr17:39441586 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(192): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.212-909C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441586 | |||||||
| chr17:39441760 | C | G | 1 | a0001c0001t0001g0027 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.212-1083G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441760 | |||||||
| chr17:39441857 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.212-1180G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39441857 | |||||||
| chr17:39442080 | ACGACAGA others(10): Show |
A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.212-1420_212-1404d others(19): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442080 | |||||||
| chr17:39442105 | G | GA | 40 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0051 others(37): Show |
41 | HG01123.hp1 HG01943.hp1 HG01981.hp1 others(38): Show |
intron_variant | MODIFIER | c.212-1429dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442105 | |||||||
| chr17:39442468 | GC | G | 17 | a0001c0001t0002g0182 a0001c0001t0002g0254 a0001c0001t0002g0255 others(14): Show |
18 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+1081delG | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442468 | |||||||
| chr17:39442524 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.211+1026C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442524 | |||||||
| chr17:39442589 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(199): Show |
204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.211+961T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442589 | |||||||
| chr17:39442598 | G | GA | 42 | a0001c0001t0001g0260 a0001c0001t0002g0153 a0001c0001t0002g0156 others(39): Show |
42 | HG00423.hp2 HG00621.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.211+951dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442598 | |||||||
| chr17:39442598 | GA | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(102): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.211+951delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442598 | |||||||
| chr17:39442645 | G | A | 8 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0150 others(5): Show |
8 | HG01255.hp2 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+905C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442645 | |||||||
| chr17:39442663 | T | C | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.211+887A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442663 | |||||||
| chr17:39442677 | T | C | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.211+873A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442677 | |||||||
| chr17:39442905 | C | CA | 55 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0030 others(52): Show |
55 | HG00423.hp1 HG00621.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.211+644dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442905 | |||||||
| chr17:39442905 | CA | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0002g0153 others(23): Show |
27 | HG01081.hp2 HG01515.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.211+644delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442905 | |||||||
| chr17:39442945 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.211+605G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442945 | |||||||
| chr17:39442996 | C | CT | 91 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0034 others(88): Show |
94 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.211+553dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442996 | |||||||
| chr17:39442996 | C | CTT | 26 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(23): Show |
26 | HG00423.hp2 HG01123.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.211+552_211+553dup others(2): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442996 | |||||||
| chr17:39442999 | T | A | 1 | a0001c0001t0002g0258 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.211+551A>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39442999 | |||||||
| chr17:39443126 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.211+424G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39443126 | |||||||
| chr17:39443158 | C | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.211+392G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39443158 | |||||||
| chr17:39443176 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.211+374T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39443176 | |||||||
| chr17:39443232 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0146 |
2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.211+318G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39443232 | |||||||
| chr17:39443320 | C | T | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.211+230G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39443320 | |||||||
| chr17:39443411 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.211+139A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39443411 | |||||||
| chr17:39443461 | C | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.211+89G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 3/16 | chr17 | 39443461 | |||||||
| chr17:39443809 | C | CAAAGGAA others(2): Show |
195 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(192): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.133-182_133-181ins others(9): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39443809 | |||||||
| chr17:39443973 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.133-345T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39443973 | |||||||
| chr17:39444133 | A | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.133-505T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444133 | |||||||
| chr17:39444368 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.133-740C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444368 | |||||||
| chr17:39444441 | A | G | 1 | a0007c0009t0002g0244 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.133-813T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444441 | |||||||
| chr17:39444508 | A | C | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.133-880T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444508 | |||||||
| chr17:39444812 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133-1184A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444812 | |||||||
| chr17:39444864 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.133-1236T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444864 | |||||||
| chr17:39444894 | C | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(139): Show |
143 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.133-1266G>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444894 | |||||||
| chr17:39444898 | A | C | 7 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0002g0251 others(4): Show |
7 | HG02129.hp1 HG02132.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-1270T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39444898 | |||||||
| chr17:39445217 | C | CT | 5 | a0001c0001t0001g0111 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-1590dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39445217 | |||||||
| chr17:39445281 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0145 |
2 | HG01106.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.133-1653A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39445281 | |||||||
| chr17:39445453 | C | T | 1 | a0001c0001t0002g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.133-1825G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39445453 | |||||||
| chr17:39445502 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(192): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.133-1874T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39445502 | |||||||
| chr17:39445539 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.133-1911G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39445539 | |||||||
| chr17:39445779 | A | C | 2 | a0001c0001t0002g0240 a0001c0001t0004g0243 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.132+2019T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39445779 | |||||||
| chr17:39445906 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.132+1892C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39445906 | |||||||
| chr17:39446014 | C | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02602.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.132+1784G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446014 | |||||||
| chr17:39446029 | TA | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0002g0153 others(6): Show |
9 | HG01070.hp1 HG01256.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+1768delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446029 | |||||||
| chr17:39446211 | G | A | 31 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0259 others(28): Show |
32 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.132+1587C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446211 | |||||||
| chr17:39446449 | C | CA | 31 | a0001c0001t0001g0012 a0001c0001t0001g0273 a0001c0001t0002g0154 others(28): Show |
31 | HG01109.hp1 HG01109.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.132+1348dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446449 | |||||||
| chr17:39446449 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0020 others(98): Show |
102 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.132+1348delT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446449 | |||||||
| chr17:39446508 | G | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.132+1290C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446508 | |||||||
| chr17:39446635 | G | C | 1 | a0001c0001t0002g0228 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.132+1163C>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446635 | |||||||
| chr17:39446646 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(200): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.132+1152A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446646 | |||||||
| chr17:39446739 | A | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG01071.hp1 HG01256.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+1059T>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446739 | |||||||
| chr17:39446778 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.132+1020T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39446778 | |||||||
| chr17:39447126 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.132+672G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447126 | |||||||
| chr17:39447142 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.132+656C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447142 | |||||||
| chr17:39447387 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.132+411C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447387 | |||||||
| chr17:39447394 | T | TA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.132+403dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447394 | |||||||
| chr17:39447521 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(139): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.132+277A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447521 | |||||||
| chr17:39447612 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.132+186C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447612 | |||||||
| chr17:39447742 | G | T | 16 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(13): Show |
16 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+56C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 2/16 | chr17 | 39447742 | |||||||
| chr17:39448101 | G | A | 31 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0259 others(28): Show |
32 | HG01070.hp2 HG01071.hp2 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-197C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448101 | |||||||
| chr17:39448125 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.26-221T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448125 | |||||||
| chr17:39448135 | C | CT | 18 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0030 others(15): Show |
18 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-232dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448135 | |||||||
| chr17:39448135 | CT | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0002g0182 others(5): Show |
8 | HG01081.hp2 HG01975.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.26-232delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448135 | |||||||
| chr17:39448190 | G | A | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.26-286C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448190 | |||||||
| chr17:39448319 | G | A | 5 | a0001c0001t0002g0153 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-415C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448319 | |||||||
| chr17:39448497 | C | G | 10 | a0001c0001t0002g0168 a0001c0001t0002g0183 a0001c0001t0002g0184 others(7): Show |
10 | HG02109.hp2 HG02486.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-593G>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448497 | |||||||
| chr17:39448548 | C | CA | 18 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(15): Show |
18 | HG00423.hp1 HG01070.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.26-645dupT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448548 | |||||||
| chr17:39448548 | C | CAA | 31 | a0001c0001t0001g0178 a0001c0001t0001g0259 a0001c0001t0001g0260 others(28): Show |
32 | HG01071.hp2 HG01081.hp2 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.26-646_26-645dupTT | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448548 | |||||||
| chr17:39448597 | A | T | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-693T>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448597 | |||||||
| chr17:39448841 | G | A | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.26-937C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448841 | |||||||
| chr17:39448849 | C | T | 15 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(12): Show |
15 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.26-945G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448849 | |||||||
| chr17:39448957 | A | G | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.26-1053T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39448957 | |||||||
| chr17:39449028 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.26-1124T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449028 | |||||||
| chr17:39449111 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.26-1207A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449111 | |||||||
| chr17:39449178 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.26-1274C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449178 | |||||||
| chr17:39449300 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.26-1396G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449300 | |||||||
| chr17:39449514 | CT | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(142): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.25+1523delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449514 | |||||||
| chr17:39449809 | C | CT | 18 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0273 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+1228dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449809 | |||||||
| chr17:39449809 | CT | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0029 others(127): Show |
131 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.25+1228delA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449809 | |||||||
| chr17:39449839 | A | G | 15 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(12): Show |
15 | HG02451.hp1 HG02559.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.25+1199T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449839 | |||||||
| chr17:39449844 | C | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.25+1194G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449844 | |||||||
| chr17:39449943 | TAGCTGGG others(5): Show |
T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.25+1083_25+1094del others(12): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39449943 | |||||||
| chr17:39450122 | A | AT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(142): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.25+915dupA | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39450122 | |||||||
| chr17:39450180 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.25+858C>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39450180 | |||||||
| chr17:39450200 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0001g0274 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.25+838C>T | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39450200 | |||||||
| chr17:39450555 | T | C | 1 | a0001c0002t0006g0275 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.25+483A>G | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39450555 | |||||||
| chr17:39450623 | C | T | 1 | a0003c0007t0010g0007 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.25+415G>A | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39450623 | |||||||
| chr17:39450722 | A | G | 1 | a0001c0002t0002g0006 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.25+316T>C | MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 1/16 | chr17 | 39450722 |